A central goal of HIV-1 vaccine research is the elicitation of antibodies capable of neutralizing diverse primary isolates of HIV-1. Here we show that focusing the immune response to exposed N-terminal residues of the fusion peptide, a critical component of the viral entry machinery and the epitope of antibodies elicited by HIV-1 infection, through immunization with fusion peptide-coupled carriers and prefusion stabilized envelope trimers, induces cross-clade neutralizing responses. In mice, these immunogens elicited monoclonal antibodies capable of neutralizing up to 31% of a cross-clade panel of 208 HIV-1 strains. Crystal and cryoelectron microscopy structures of these antibodies revealed fusion peptide conformational diversity as a molecular explanation for the cross-clade neutralization. Immunization of guinea pigs and rhesus macaques induced similarly broad fusion peptide-directed neutralizing responses, suggesting translatability. The N terminus of the HIV-1 fusion peptide is thus a promising target of vaccine efforts aimed at eliciting broadly neutralizing antibodies.


Since crossing from chimpanzees ~100 years ago1, HIV-1 has evolved to be one of the more diverse viruses to infect humans2. While antibodies capable of neutralizing ~50% of circulating HIV-1 strains arise in half of those infected after several years3, vaccine elicitation of antibodies capable of neutralizing divergent strains of HIV-1 remains an unsolved problem: antibodies elicited by current candidate vaccines fail to neutralize more than a small fraction of the diverse primary isolates that typify transmitted strains of HIV-14,5.

We and others have isolated broadly neutralizing antibodies from HIV-1-infected donors and coupled antibody identification with structural characterization to delineate sites of vulnerability to neutralizing antibodies6,7. These antibodies target the viral entry machinery, the envelope (Env) trimer, composed of three glycoprotein (gp) 120 subunits and three gp41 subunits. Dozens of structurally defined epitopes have been determined that can be categorized into a handful of Env regions. The majority of identified neutralizing antibodies have characteristics that may make them difficult to elicit by vaccination, including those to the CD4-binding site8,9, where extensive somatic hypermutation (SHM) appears to be required10,11,12; those to a quaternary site at the trimer apex13,14,15,16, where unusual recombination appears to be required13,14,17,18; those to a glycan-V3 supersite19,20,21, where recognition of N-linked glycan appears to be required20,21,22; and those to the membrane-proximal external region23,24,25,26, where co-recognition of membrane27,28,29 and immune tolerance appear to be required30.

Recently, we identified an antibody, N123-VRC34.0131, named for donor (N123), lineage (VRC34), and clone number (01), and hereafter referenced without donor prefix. VRC34.01 targets primarily the conserved N-terminal region of the HIV-1 fusion peptide (FP), a critical component of viral entry machinery32. FP is composed of 15–20 hydrophobic amino acids at the N terminus of the gp41 subunit of HIV Env and had been thought to be poorly immunogenic: hidden from the immune system in the native prefusion state of Env and buried in the cell membrane after Env rearranges into the postfusion state. The VRC34.01 antibody, however, revealed the N-terminal half of FP to be a site of neutralization vulnerability. VRC34.01 directs the majority of its binding energy to eight N-terminal residues of FP, with the rest coming from interactions with Env including glycan N8831. The ability to neutralize HIV-1 through recognition of a linear peptide that is both conserved in sequence and exposed in the prefusion, closed conformation of Env, suggested that the site of vulnerability defined by VRC34.01 might be amenable to epitope-based approaches to vaccine design. In this study, we describe an antibody-to-vaccine development process. Beginning with the epitope of VRC34.01, we engineered immunogens with antigenic specificity for FP-directed antibodies, immunized C57BL/6 mice, and analyzed the resultant antibodies. Based on these analyses, we devised second-generation immunization regimens that generated improved neutralizing monoclonal antibodies. We extracted insights from the murine immunizations and applied these to immunize guinea pigs and rhesus macaques. While breadth, potency, and consistency need to be improved, overall, these vaccine studies demonstrated the ability, in standard vaccine-test species, to induce serum responses capable of neutralizing a substantial fraction of primary isolate strains representative of the global diversity of HIV-1.

Fusion peptide-based immunogens

The eight N-terminal residues of FP were chosen as a vaccine target, based on their recognition by antibody VRC34.01 in co-crystal structures and on molecular dynamics simulations, which showed these residues to be exposed and flexible in conformation31. To obtain immunogens capable of eliciting FP-directed antibodies, we used structure-based design to engineer FP-containing immunogens and assessed their antigenic specificity against a panel of antibodies encompassing both broadly neutralizing antibodies and poorly or non-neutralizing antibodies, with an emphasis on antibodies reported to engage FP as part of their recognized epitope such as ACS20233 and PGT15134 (Fig. 1a). We used an antigenicity score derived from the binding affinity of epitope-specific neutralizing and weakly or non-neutralizing antibodies (see Methods) to estimate the epitope-specific suitability of each immunogen (Supplementary Fig. 1a). We produced epitope scaffolds that incorporated the eight N-terminal amino acids of FP and, in some cases, included sites of N-linked glycosylation, which we positioned analogously to FP and glycan N88 in the VRC34.01 epitope. We characterized two scaffolds, which were trimeric and tetrameric, from Protein Data Bank (PDB) 3HSH35 and 1SLF36, respectively, and also assessed epitope scaffolds engineered from PDB 1M6T37 and from PDB 1Y1238, which we previously described31 (Supplementary Fig. 1b–g); the oligomeric scaffolds generally showed stronger binding to the FP-directed antibodies.

Fig. 1: Design, properties, and immunogenicity of FP immunogens based on the epitope of antibody VRC34.01.
Fig. 1

a, Structure-based design, antigenic characteristics, and EM structure of FP immunogens. The glycosylated structure of the HIV-1 Env trimer is shown at far left, with exposed N terminus of FP highlighted in red. Subsequent images show site recognized by VRC34.01 antibody, schematics and antigenicity of FP immunogens, and negative stain EM of FP-KLH (see Supplementary Fig. 1 for details of FP antigenicity). For the EM study, n = 3 independent experiments were performed with similar results. b, Immunization regimen 1. At day 52, mouse spleens were harvested and hybridomas created. c, ELISA and neutralization of serum from regimen 1-immunized mice. Protein probes used for ELISA are defined in top row and include BG505 SOSIP.664 (green), FP-epitope scaffold based on PDB 1M6T (red), and 1M6T scaffold with no FP (blue). Column 1 defines mouse identification number and subsequent columns show ELISA and neutralization. ELISAs are shown as a function of serum dilution for prebleed, days 21, 35, and 52 (ELISA curves colored according to probe, with sera mostly unreactive with IM6T scaffold with no FP; OD450 is tthe optical density at the 450-nm wavelength). Neutralization (ID50, ID80) values provided for day-52 serum; see Supplementary Fig. 2a for neutralization details. d, Immunization regimen 2. At day 38, mouse spleens were harvested and hybridomas created. e, ELISA and serum neutralization of serum from regimen 2-immunized mice, displayed as in c.

We also created a FP-carrier protein conjugate, by coupling the eight N-terminal residues of FP through an appended C-terminal cysteine using a bifunctional reagent to covalently link to lysine residues in keyhole limpet hemocyanin (KLH), a carrier protein often used to improve immunogenicity39. The resultant FP8-KLH was robustly recognized by FP-directed antibodies and stable to extremes of temperature and osmolality, and at pH 10.0, but not at pH 3.5; and negative-stain electron microscopy (EM) revealed that FP-conjugated KLH retained the barrel shape of KLH (Supplementary Fig. 1b,c,h,i). When assessed with the FP-antigenicity score (Fig. 1a), FP8-KLH was superior to the FP-epitope scaffolds and similar to stabilized Env trimers, such as the SOSIP.66440 or DS-SOSIP41 trimers from the clade A strain BG505.

Immunogens with high FP-antigenic specificity induce FP-directed neutralizing responses

To assess the ability of the first-generation epitope-based vaccine immunogens to elicit neutralizing responses, we tested immunization regimens using the two immunogens with the highest FP-antigenicity scores, FP8-KLH and stabilized Env trimer. In an initial experiment, 4 C57BL/6 mice each received 50 µg of BG505 SOSIP Env trimer and were boosted with 25 µg of FP8-KLH at day 14 (Fig. 1b). After a second boost at day 28, strong FP responses in enzyme-linked immunosorbent assay (ELISA) were observed at day 35. After a final boost at day 49, we tested day-52 serum for neutralization of the Env pseudovirus BG505 and for neutralization of a BG505 Env variant missing glycans at positions 88 or 611 (Δ88 or Δ611, respectively), as these Env variants are more sensitive to FP-directed antibodies31. While serum neutralization of wild-type BG505 generally did not pass our ID50 (reciprocal plasma or serum dilutions causing a 50% reduction) threshold for murine neutralization (at least 1:40 and at least twofold above background), we did observe unambiguous serum neutralization for the Δ88+611 glycan-deleted variant of BG505 by all 4 of the mice (Fig. 1c and Supplementary Fig. 2a).

In a subsequent experiment, 3 mice each received 25 µg of FP-KLH, followed by boosts at day 14 and day 35 (Fig. 1d). Serum ELISAs revealed Env trimer recognition in mouse 2586 at days 21 and 38; this also appeared in a second mouse after the final boost. We tested day-38 serum for neutralization and observed neutralization for the Δ88+611 glycan-deleted variant of BG505 by two of the sera (Fig. 1e and Supplementary Fig. 2a).

First generation FP-directed antibodies neutralize up to ~10% of HIV-1 strains

To provide insight into the antibodies elicited by FP-containing immunogens, we selected B cell hybridomas capable of binding both BG505 SOSIP trimer and FP-1M6T scaffold, using B cells from mouse 1868 (immunized with Env trimer and FP-KLH) and mouse 2586 (immunized with FP-KLH only). Sequences of seven hybridomas from mouse 1868 and five hybridomas from mouse 2586 revealed seven vaccine-elicited (v) antibody lineages (vFP1–vFP7), which could be segregated into three classes defined by B cell ontogeny and structural mode of recognition6 and which we named vFP1, vFP5, and vFP6, after the first identified member of each class (Supplementary Fig. 3a,b and Supplementary Tables 1 and 2).

We tested neutralization of the 12 vFP antibodies on a panel of wild-type and glycan-deleted HIV-1 variants. Clear neutralization of wild-type HIV-1 strains was observed with only a few of the vFP1-class antibodies (vFP1.01, vFP7.04, and vFP7.05). We assessed the three best vFP1-class antibodies along with antibody vFP5.01 on a well-characterized panel of 208 Env pseudoviruses5, encompassing diverse strains of primary isolates from all of the major clades, of which 154 were resistant to neutralization by CD4-induced antibodies 17b and 48d, the V3-directed antibodies 447-52D and 3074, and antibody F105, which recognized open conformations of Env (Supplementary Fig. 3c and Supplementary Table 3a). Notably, vFP1.01 neutralized 18 strains at 50 µg/mL (8.2% breadth on 208-strain panel; 7.7% breadth on 154-resistant strain panel), while vFP7.04 neutralized 20 strains at 50 µg/mL (9.6% breadth on 208-strain panel; 8.3% breadth on 154-resistant strain panel). vFP5.01, by contrast, neutralized only two strains, both sensitive to V3 and CD4-induced antibodies. Overall, neutralization by these first-generation monoclonal antibodies was of limited breadth and potency, although the best vFP antibodies could neutralize selected diverse strains of HIV-1.

Disparate antibody-bound FP conformations

To provide insight into the structural basis for neutralization by the first-generation vaccine-elicited antibodies, we determined crystal structures for the antigen-binding fragment (Fab) of vFP1.01 and vFP5.01 antibodies in complex with the eight N-terminal residues of FP (Ala512–Phe519) at 2.0- and 1.5-Å resolutions, respectively (Supplementary Table 4a and Supplementary Fig. 4; also see expanded views in Fig. 2a,b). The vFP1.01 co-crystals with FP were orthorhombic with four molecules per asymmetric unit, and in all four independent copies, Fab and FP assumed similar conformations, with FP adopting a curved structure with no intrachain-backbone hydrogen bonds. The N terminus of FP (Ala512) was buried between heavy and light chains, with the amino terminus forming a buried salt bridge with Glu34vFP1.01-LC, which was germline-encoded and shielded from solvent by a tetratyrosine cage, comprising tyrosines at residues 27DvFP1.01-LC, 32vFP1.01-LC, 96vFP1.01-LC, and 98vFP1.01-HC (for clarity, we reference the molecule as a subscript for all molecules other than HIV Env by antibody name and HC or LC for heavy or light chain, respectively). The FP-main chain paralleled the curvature of the vFP1.01 complementarity-determining region (CDR) H3, albeit with opposite orientation, up to residue Ile515, which packed against the body of the heavy chain before extending from antibody into the main body of the trimer with Gly516–Phe519 (Supplementary Fig. 4a,b).

Fig. 2: FP assumes disparate antibody-bound conformations, with neutralization restricted to a select angle of trimer approach.
Fig. 2

a, Structural definition of vFP1.01 recognition. Top: cryo-EM reconstruction at 8.6-Å resolution (density shown in gray) of Fab vFP1.01 in complex with BG505 DS-SOSIP trimer. Expanded view: crystal structure of Env trimer and FP-bound Fab vFP1.01 at 2.0-Å resolution, as modeled into the cryo-EM map by rigid-body docking. Env trimer for gp120 (green) and gp41 (gray), Fab vFP1.01 heavy chain (cyan) and light chain (yellow), and FP N terminus (purple). Surface areas provided for N-terminal region of FP. b, As in a, but for vFP5.01 (blue and yellow) and FP (pink). Note that the angle of the lower right Fab differs from the angles of the other two. c, Comparison of FP bound by vFP1.01 vs. VRC34.01, with antibody shown in ribbons and FP in stick representation. d, As in c, but for vFP5.01. e, Angle of recognition and Fv-domain overlap for vFP1.01, vFP5.01, and VRC34.01. Measured angles (red) are between antibody angle of approach and Env-trimer axis (left, with viral membrane located below trimer) and between antibody angle of approach parallel to viral membrane and Env protomer (right, looking down trimer axis toward viral membrane).

The vFP5.01 co-crystals with FP were monoclinic, with one molecule per asymmetric unit. vFP5.01 bound FP at the interface of heavy and light chains, with the peptide adopting an overall hook structure: starting with a surface-exposed Ala512, dipping into the hydrophobic antibody interface with aliphatic side chains of Val513 and Ile515 anchoring the FP N terminus, before turning at Gly516 and extending from antibody toward Env (Supplementary Fig. 4c,d).

Comparison of antibody-bound crystal structures indicated substantial differences in FP conformation (Fig. 2c,d). While antibodies VRC34.01, vFP1.01, and vFP5.01 recognized the N terminus of FP by using a similar region at the CDR-H3–CDR-L3 interface of each antibody, the conformations of the antibody-bound FPs were substantially different: the vFP1.01-bound FP formed a U-shaped structure focused at the heavy–light interface, vFP5.01 bound FP in an extended conformation to interact with CDR H3, and VRC34.01 bound FP in an extended conformation to interact with CDR H1. To place these disparate antibody-recognized conformations of FP into a more general context, we used principal component analysis to cluster N-terminal FP conformations from a molecular dynamics simulation of fully glycosylated HIV-1 Env. Four prevalent clusters of FP conformations were observed (Supplementary Fig. 4e,f), with FP-directed antibodies recognizing disparate but prevalent conformations of FP.

Restricted angle of approach for FP-directed neutralization

To position the vFP1.01 and vFP5.01 structures with FP into the context of the HIV-1 Env trimer, we collected cryo-EM data for these FP-directed antibodies complexed to the BG505 SOSIP trimer. With Fab vFP1.01, approximately 14,000 particles yielded an 8.6-Å resolution reconstruction after threefold averaging (Supplementary Fig. 5a–e); the resulting structure (Fig. 2a) showed three Fabs laterally interacting with the Env trimer. With Fab vFP5.01, several particle classes were observed yielding reconstructions at 14.7- and 19.6-Å resolutions (Supplementary Fig. 5f–h); these asymmetric reconstructions indicated each of the vFP5.01 Fabs to approach Env differently (Fig. 2b).

To provide insight into recognition of the Env trimer, we analyzed the approach angle of the FP-recognizing antibodies (Fig. 2e). Overall, the approach of antibodies directed primarily to FP and capable of neutralizing diverse HIV-1 strains was similar, suggesting restrictions on trimer approach for effective FP-directed neutralization.

Considerations for improved immunizations

Analysis of the first-generation antibodies indicated that effective FP-directed neutralization would occur preferentially at a restricted angle of trimer approach, thereby suggesting that boosting with Env trimer might elicit improved neutralization. We sought additional clues from analysis of the first-generation vFP antibodies to improve FP immunization.

To provide insight into sequence requirements for neutralization, we created a panel of peptides comprising Ala and Gly mutants of the N terminus of FP and screened for recognition by vaccine-elicited antibodies and by VRC34.01 (Supplementary Fig. 6a and Supplementary Table 5). The Ala–Gly mutants only affected vFP1.01 recognition if they occurred within the first four residues of FP (512–515). For vFP5.01, a more extensive range was observed, with alterations to Ala–Gly at residues 513, 514, 515, 516, and 519 affecting recognition. VRC34.01 recognition was intermediate between vFP1.01 and vFP5.01, being sensitive to changes at 512, 513, 515, and 516, and partially sensitive to changes at 518 and 519. These results indicated a preference for N-terminal residues for effective neutralization, thereby suggesting that N-terminal focusing might improve neutralization of the vaccine-elicited antibodies.

Although we did not observe a substantial improvement in neutralization titers upon Env priming (Fig. 1), we nevertheless analyzed the degree of affinity maturation for vFP1-class antibodies, as this would lend insight into the induction of these antibodies. We identified vFP1-class antibodies from three additional mice, two of them (1882 and 1883) primed with Env trimer and one (2602) immunized with only FP-KLH (Supplementary Fig. 7a). Notably, vFP1-class antibodies primed with Env trimer showed higher SHM with statistical significance (P = 0.0046; Supplementary Fig. 7b). Thus, while Env-trimer priming did not improve neutralization, it did appear to prime vFP1-class antibodies.

Second-generation FP-directed antibodies neutralize up to 31% of HIV-1 strains

To elicit improved FP-directed antibodies, we tested 11 immunization regimens on 16 C57BL/6 mice (Supplementary Fig. 8a). The vaccine regimens included a BG505 SOSIP trimer prime and various FP-KLH boosts, along with a BG505 DS-SOSIP boost on a subset of 5 of the mice. The FP-KLH boosts used different lengths of FP, ranging from FP6 through FP10, which incorporated 6–10 residues from the N-terminal FP sequence of strain BG505. Serum neutralization titers for the 5 trimer-boosted animals were especially improved, reaching an ID50 as high as 77,379 (mouse 2716) for the glycan-deleted (Δ88+611) BG505 (Supplementary Fig. 8a,b). We tested the serum neutralization for the 5 trimer-boosted mice on a panel of 10 selected wild-type strains, which were chosen for their sensitivity to VRC34.01 or vFP1.01 and to encompass divergent HIV-1 clades (Supplementary Figs. 2b and 8c). While modest neutralization from these 5 sera was observed against the selected strains, serum from mouse 2716 achieved ID50 neutralization against all ten of these strains and ID80 against seven of them. Analysis by peptide competition indicated neutralization by the mouse 2716 serum to be targeted primarily to FP (Supplementary Fig. 2c).

For each of the 16 immunized C57BL/6 mice, we isolated and characterized monoclonal antibodies. These could be parsed into 21 lineages, vFP12–vFP32 (Supplementary Table 1a–c), and we screened each of the vFP antibodies against two wild-type viruses, clade A BG505 and clade B 3988.25; 24 antibodies showed wild-type neutralization, with most neutralizing 70% or more of the ten-strain panel (Supplementary Table 3b).

We chose two antibodies, 2712-vFP16.02 and 2716-vFP20.01, for in-depth assessment (vaccine-elicited FP antibodies were named for mouse ID-lineage.clone, with antibody 2716-vFP20.01 being clone 01 from lineage vFP20 isolated from mouse ID 2716). Notably, on the 208-strain panel, these two antibodies achieved 31% and 27% neutralization breadth, respectively, when assessed at a maximum IC50 level of 50 µg/mL (Fig. 3 and Supplementary Table 3a). The breadth and potency of these two vFP antibodies were similar to that of antibody 2G12 (Supplementary Fig. 11b), which has been shown to delay rebound and to induce selection pressure on the viral quasispecies when passively infused42,43,44. Neutralization extended to multiple clades, including clades A, B, and C, but for several clades, including clades AC, AG, D, CD, and G, no neutralization was observed. In the neutralized clades, the immunized FP8 sequence was generally present, whereas in the non-neutralized clades, this FP8 sequence was not present (in clade AE, the prevalent FP8 sequences included changes in the C-terminal region of FP8 (Supplementary Table 6), which were apparently tolerated by both vFP16.02 and vFP20.01 antibodies). We observed strong correlation between FP-directed antibody breadth on the 208-strain panel and the 58-strain panel with identical FP8 sequences, indicating overall breadth of the vFP antibodies to correlate with the ability to neutralize strains with the most prevalent FP8 sequence (Fig. 3). These results provide proof of principle for the ability of FP-epitope focusing to induce FP-directed antibodies with promising neutralization breadth.

Fig. 3: FP-directed vaccine-elicited antibodies neutralize up to 31% of HIV-1.
Fig. 3

Neutralization dendrograms display the diversity of tested viral strains, with branches colored according to neutralization potency (non-neutralized branches shown in gray). Top row: 208-strain panel for vaccine-elicited antibodies vFP16.02 and vFP20.01. Bottom left: 58-strain panel, displaying only branches with FP8 = AVGIGAVF. Bottom right: comparison of breadth on 58- and 208-strain panels shown with Pearson correlation (n = 7 antibodies).

Structures and Env interactions of second-generation antibodies vFP16.02 and vFP20.01

To gain insight into the cross-clade breadth observed with vFP16.02 and vFP20.01 antibodies, we determined their crystal structures in complex with FP (Supplementary Fig. 4g,h) and their cryo-EM structures in complex with HIV-1 Env trimer (Fig. 4). The crystal structures with FP revealed highly similar recognition of residues 512–517, with vFP1-class antibodies constraining little of the FP conformation beyond residue 517 (Supplementary Fig. 4g,h and Supplementary Table 4a). The cryo-EM data were collected on a quaternary complex with BG505 DS-SOSIP trimer bound by antibodies PGT122 and VRC03, in addition to vFP16.02 or vFP20.01; the added antibodies increased the size of the complex and provided fiducial markers allowing better particle visualization and alignment. The resultant reconstructions displayed resolutions of 3.6 and 3.8 Å, respectively, when calculated according to the FSC 0.143 gold-standard criterion with soft-edged masks from which flexible constant regions had been removed (Fig. 4, Supplementary Fig. 9a–f, and Supplementary Table 4b). In the reconstructions, we observed electron density for the vFP16.02 and vFP20.01 antibodies focused around the fusion peptide, with density becoming weaker farther from the fusion peptide site of recognition (Supplementary Fig. 10a,b).

Fig. 4: Substantial glycan contacts by vaccine-elicited FP-directed antibodies.
Fig. 4

a, Cryo-EM map of quaternary complex with antibody 2712-vFP16.02, segmented by components at a contour level that allowed visualization of Fv domains of antibodies (also see Supplementary Figs. 9 and 10). b, As in a, but with 2716-vFP20.01. c, Details of vFP16.02 interaction. Right: experimental EM density in blue mesh, with contour level adjusted to allow visualizing of partially ordered glycan. Residues altered by SHM highlighted in cyan. Antibody vFP16.02 contacts both FP and neighboring glycans to achieve 31% breadth. d, As in c, but for vFP20.01. e, Sequence alignment of vaccine-elicited FP-directed antibodies and origin genes. FP contacts (red highlight), glycan contacts (green rectangles), and SHM (cyan font) are highlighted. Additional Env contacts are indicated by double underlining. Because the density from the cryo-EM reconstructions was not always sufficient to allow for atomic-level fitting, contacts shown with dotted green rectangles were inferred.

Glycan contacts between vFP antibodies and Env trimer were observed (Fig. 4c,d), and SHM was observed to occur preferentially at the interface with Env, especially involving interactions with FP and with N-linked glycan (Fig. 4e). In both antibody–Env complexes, glycans N448 and N611 displayed similar orientations, with glycan N448 buttressed by the light chain on one side and by glycan N295 on the other, and with glycan N611 projecting from a neighboring Env protomer directed toward the antibody heavy chain. Glycan N88 also displayed ordered density for its protein-proximal sugars, though this differed in the two antibody complexes: in vFP16.02, substantial ordering was observed, with the glycan lodged between gp41 and the heavy chain (Fig. 4c); in vFP20.01, glycan N88 was less ordered and assumed a substantially different conformation to accommodate the SHM-altered Gly56TyrvFP20.01-HC side chain (Fig. 4d). We note that even though removal of glycans neighboring FP (for example, glycan 611) improved neutralization by these antibodies, resistance analysis (Supplementary Table 7) indicated that neutralization in the 208-strain panel was not dependent on the absence of FP-neighboring glycans. Overall, the structures indicated murine vFP antibodies with promising breadth to substantially accommodate, if not partially recognize, FP-proximal N-linked glycan.

Translation of murine vaccine regimens into guinea pigs and nonhuman primates

We extracted insights from the murine immunization regimens, such as trimer boost and FP N-terminal focusing, and applied these to guinea pigs and rhesus macaques (nonhuman primates; NHPs). We immunized 5 guinea pigs using a scheme modeled on the mouse-2716 immunization regimen (Fig. 5a). At week 28, 4 of 5 guinea pigs showed some heterologous virus neutralization on the ten-strain panel. When compared to guinea pigs immunized with DS-SOSIP alone (Supplementary Fig. 7e), the ten-strain breadth induced by the FP-KLH-primed DS-SOSIP boost was significantly higher than that induced by DS-SOSIP alone (Fig. 5a,b).

Fig. 5: Immunization of guinea pigs and NHPs with FP-coupled carriers and DS-SOSIP trimer elicits heterologous neutralizing responses.
Fig. 5

a, Elicitation of serum neutralizing responses in guinea pigs. Immunization regimen and week 28 serum ID50 titers as measured on a panel of 10 wild-type strains, 5 with complete glycans around FP and 5 naturally missing glycans at sites shown. Also shown are titers for Δ88, Δ611, and Δ88+611 glycan-deleted variants of BG505. b, Plot comparing guinea pig-serum neutralization breadth for FP-KLH prime + DS-SOSIP trimer-boost regimen versus DS-SOSIP-alone regimen (one-tailed Mann–Whitney test; see Supplementary Fig. 7 for DS-SOSIP alone immunizations at 0, 4, and 16 weeks; n = 5 animals for each group). c, Elicitation of heterologous neutralizing responses in rhesus macaques. Immunization scheme and week 46 serum titers assessed and displayed as in a. d, Plot comparing NHP serum neutralization breadth for immunization regimens, displayed as in b; n = 5 animals for each group.

For NHP, we also used a regimen similar to that used for mouse 2716, but omitted the initial trimer prime and used three trimer boosts so that we could compare to NHPs immunized with trimer only. We used a total of 5 FP-KLH primes with FP peptides of lengths eight, eight, eight, seven, and six. At week 46, 4 of 5 NHP plasmas showed heterologous virus neutralization on the ten-strain panel (Fig. 5c,d). As seen in the GP immunization study, this breadth of neutralization by NHP plasma was higher than that induced by immunization with DS-SOSIP alone (Supplementary Fig. 7f)45.

We further assessed week-46 plasma from all 5 NHP on a 58-strain subset of the 208-strain panel, restricted to strains for which the sequence of FP was AVGIGAVF, the most prevalent FP sequence and the sequence in the FP8-KLH and BG505 DS-SOSIP immunogens. At a 1:20 dilution, 3 of 5 NHP plasmas showed substantial neutralization breadth, with the broadest, NHP DF1W, achieving ID50 neutralization on 41 of 58 strains (70%) and ID80 neutralization of 13 of 58 strains (22%; Fig. 6a and Supplementary Table 3c). Neutralization competition of the NHP DF1W plasma tested against neutralization-resistant HIV-1 strains with complete glycan around FP from four different clades indicated that a linear FP, matching the immunogen sequence, could adsorb virtually all of the neutralizing activity (Fig. 6b and Supplementary Fig. 2d). A dendrogram of these 58 Env strains (Fig. 6c) indicated that neutralization was distributed over several clades, consistent with the distribution of the immunized FP8 sequence in HIV-1. Additionally, the neutralization fingerprints of the three NHP plasmas, with substantial breadth clustered next to the neutralization fingerprints of the murine vFP1-class antibodies (Fig. 6d), provided strong indication for the similarity of induced murine and NHP immune responses.

Fig. 6: Patterns of neutralization indicate broad FP-directed responses in mice and NHP are related.
Fig. 6

a, Neutralization on a 58-strain panel, comprising strains from the 208-strain panel with the FP sequence AVGIGAVF matching both FP8-KLH and BG505 trimer immunogens. Top: IC50 values for FP-directed antibodies. Bottom: ID50 titers for NHP plasma: top 5 rows, FP-KLH primer + DS-SOSIP trimer-boost regimen at week 46, 2 weeks after third trimer boost; bottom row, DS-SOSIP alone regimen at week 18, 2 weeks after third trimer boost. Numbers of neutralized strains and neutralization breadths are shown. (IC80 and ID80 provided in Supplementary Table 3c and Supplementary Fig. 7.) b, Neutralization curves of NHP plasma (DF1W week 46) and control monoclonal antibodies (VRC34.01 and VRC01) on four representative strains in the presence of no peptide (black), FP (red), or an irrelevant Flag peptide (blue). Mean and s.d. of results from triplicated experiments shown (n = 3 independent experiments). c, Neutralization dendrogram (ID50) for NHP DF1W week 46 plasma on 58-strain panel, showing location of representative strains tested in b. d, Neutralization-fingerprint dendrogram calculated from 58-strain panel. Vaccine-elicited vFP antibodies (light-green background) and 3 NHP week-46 plasmas (dark-green background for 3 of 5 NHPs with sufficient neutralization to yield accurate fingerprint analysis) clustered next to each other (see also fingerprint dendrogram on 132 curated strains shown in Supplementary Fig. 11a).


The vaccine elicitation of antibodies capable of neutralizing diverse strains of HIV-1 has been a goal of HIV-1 research for over 30 years. While substantial strides have been made in the creation of prefusion-stabilized Env trimers40,41,46,47,48,49, responses elicited by these trimers have been primarily strain-specific. Here we show that focusing the immune response on the exposed N-terminal residues of FP elicits antibodies of promising neutralization breadth in multiple vaccine-test species. Several factors contributed to the successful elicitation of neutralizing antibodies. First, antibody VRC34.0131 defined a precise target—not the entire FP, but only exposed N-terminal residues—upon which to focus. Second, glycan-deleted viruses50 provided a readout sensitive enough to detect initial weak serum responses. Third, we found prefusion-closed Env trimers40 to be necessary for boosting serum responses. Most important, however, may be the characteristics of the target site—the FP N terminus—a conserved and exposed site of vulnerability, for which high conformational variability was compatible with broad neutralization (Supplementary Figs. 4e and 11c–g).

FP-directed antibodies of substantial breadth have been reported for other viral pathogens, including influenza A virus51,52, Ebola virus53,54,55, and Lassa virus56. Although the fusion peptides of these pathogens are substantially different from that of HIV-1, the generality of FP-targeted neutralizing antibodies suggests that characteristics of FP may be especially suited to vaccine targeting. Such characteristics include its conservation (related to function), its chemistry (hydrophobic residues afford high binding energy), and its exposure (FP is often proximal to a site of proteolytic activation).

Is there a neutralization limit or constraint for vFP antibodies based on viral properties (for example, related to strain-specific conformation or accessibility) other than the diversity of FP itself? A strong correlation was observed between Env trimer affinity and neutralization breadth (Supplementary Figs. 6b,c and 11d), suggesting that enhanced Env-trimer affinity would lead to increased breadth. Indeed, at tenfold higher concentration (500 µg/mL), vFP16.02 neutralized 97% (56 of 58 strains) with the immunized FP8 sequence, and 47% of the 208-strain panel (97 of 208 strains; Supplementary Table 3a). Thus, for strains with the same sequence as used in the FP immunizations, there did not appear to be an intrinsic limit to elicited FP-directed breadth.

Finally, is the observed elicitation of vFP-neutralizing antibodies in animal models translatable to humans? While broadly neutralizing antibodies against HIV-1 have been induced in animals such as cows57 and llamas58, these antibodies rely on species-specific characteristics59,60 (knob domains for cow and unpaired heavy chains for llama), which are not present in human antibodies. By contrast, there does not appear to be an intrinsic barrier to eliciting vFP antibodies in humans: genetic analysis indicates that humans have V-genes with some similarity to the germline genes of the murine vFP1-antibody class (Supplementary Fig. 12a,b), FP-directed antibodies can often be detected in HIV-1-infected donors by ELISA31, and FP-directed antibodies showed almost no indication of polyreactivity (Supplementary Fig. 12c,d). Overall, our results provide proof of principle for the ability of epitope-based vaccine design to induce FP-directed antibodies with neutralization breadth and indicate that the exposed N terminus of FP is a site of exceptional HIV-1 vaccine promise.


Peptide synthesis and peptide-carrier protein conjugate preparation

HIV-1 fusion peptides (FPs) were synthesized (GenScript) with a free amine at the N terminus. FP His-tagged peptides were synthesized (GenScript) with a six-histidine-residue tag at the C terminus. To prepare peptide-carrier protein conjugates, each peptide with a cysteine residue appended to the C terminus was conjugated to lysine residuse on the carrier protein keyhole limpet hemocyanin (KLH; Thermo-Scientific) using m-maleimidobenzoyl-N-hydroxysuccinimide ester (MBS), following the manufacturer's protocol.

Protein expression and purification

BG505 SOSIP, BG505 DS-SOSIP, and their glycan-deficient variants were expressed and purified as described previously41. FP-epitope scaffold proteins, including FP-1M6T, FP-1Y12, FP-3HSH, and FP-1SLF were expressed and purified as described previously31. vFP1.01, vFP7.04, vFP16.02, and vFP20.01 antibodies used for structure determination were prepared as below. Heavy chain plasmids, encoding the chimera of mouse variable domain and human constant domain, with HRV3C cleavage site in the hinge region; and light chain plasmids, encoding the chimera of mouse variable domain and human constant domain, were co-transfected in Expi293F cells (Thermo Fisher) using Turbo293 transfection reagent (SPEED BioSystem) according to the manufacturer's protocol. Transfected cells were incubated in shaker incubators at 120 rpm, 37 °C, 9% CO2 overnight. On the second day, one-tenth culture volume of AbBooster medium (ABI scientific) was added to each flask of transfected cells and cell cultures were incubated at 120 rpm, 33 °C, 9% CO2 for an additional 5 d. Cell culture supernatants were harvested 6 d post-transfection. IgGs were purified from the supernatants using protein A chromatography: after PBS wash and low pH glycine buffer elution, the eluate was immediately neutralized using 10% volume of 1 M Tris buffer, pH 8.0. Fabs were obtained either by HRV3C cleavage or papain digestion. The fragmented Fabs were further purified by size-exclusion chromatograph (SEC) in a Superdex 200 column (GE) with a buffer containing 5 mM HEPES, pH 7.5, and 150 mM NaCl.

Negative-stain electron microscopy

Samples were diluted with a buffer containing 20 mM HEPES, pH 7.0, and 150 mM NaCl, adsorbed to a freshly glow-discharged carbon-film grid, washed with the above buffer, and stained with 0.7% uranyl formate. Images were collected semiautomatically at a magnification of 100,000× using SerialEM61 on a FEI Tecnai T20 microscope equipped with a 2k × 2k Eagle CCD camera and operated at 200 kV. The pixel size was 0.22 nm/pixel. Particles were picked manually using the swarm mode in e2boxer from the EMAN2 software package62. Reference-free 2D classification was performed using EMAN2 and SPIDER63.

Antigenic characteristics of fusion peptide immunogens with Biolayer Interferometry and MSD-ECLIA

Antigenic characteristics of KLH-coupled fusion peptide, FP scaffolds, and BG505 Env trimers to various FP-targeting and non-FP-targeting HIV antibodies were assessed with Biolayer Interferometry on an Octet RED384 (ForteBio) instrument and with MSD-ECLIA as previously described41.

Antigenicity score

Antigenicity scores for the FP immunogens were calculated according to the metric defined in Supplementary Fig. 1a. This metric sums the average binding of neutralizing antibodies versus poorly/non-neutralizing antibodies, with binding defined as a function of the logarithm of antigen-binding affinity relative to upper and lower binding limits. This summation is weighted by the site targeted. An antigenicity score of 1 for an FP immunogen therefore indicates both high specificity and tight affinity for FP-directed neutralizing antibodies; an antigenicity score of 0 for an FP immunogen would indicate either low specificity or weak affinity for FP-directed neutralizing antibodies. In Fig. 1a, the antigenicity score was calculated with only FP-directed antibodies; we anticipate that the FP-antigenicity score for trimer immunogens would decease relative to FP-specific immunogens, such as FP8-KLH, if non-FP-directed antibodies were considered.

Mouse immunization (GenScript)

Female mice (C57BL/6) around 8 weeks old were immunized in 2-week intervals with either HIV-1 Env trimer or FP-KLH, using either Adjuplex as adjuvant (Sigma-Aldrich Inc., MO) for trimer or GS-adjuvant (GenScript) for FP-KLH. We used 50 µg of immunogens for prime immunization and 25 µg immunogens in boost immunization. Intraperitoneal (IP) injections were used for all mouse immunizations. Sera samples were collected either 7 d or 14 d after each immunization for ELISA and other analyses.

All experiments were performed in accordance with protocols reviewed and approved by GenScript's Institutional Animal Care and Use Committee (IACUC, #ANT14-003 and #ANT17-003). All mice were housed and cared for in a GenScript facility accredited by the Association for Assessment and Accreditation of Laboratory Animal Care International (AAALAC International).

Hybridoma creation and monoclonal antibody production

Terminal boosts were performed on the top responders from each immunization scheme, as assessed with ELISA, against the immunogens 3 weeks after the last immunization. Mice spleens were harvested 3 d after the terminal boost, and hybridomas were generated for monoclonal antibody selection following the standard procedure at GenScript. Monoclonal antibody selection was based on affinity to FP-scaffold (FP-1M6T) and BG505 Env trimer as measured by ELISA.

Guinea pig and NHP protocols and immunizations

For immunization studies, all animals were housed and cared for in accordance with local, state, federal, and institute policies in an American Association for Accreditation of Laboratory Animal Care-accredited facility at the Vaccine Research Center, NIAID, NIH, or at a contract facility (Bioqual Inc., MD). All animal experiments were reviewed and approved by the Animal Care and Use Committee of the Vaccine Research Center, NIAID, NIH, and covered under protocols VRC-13-431, VRC16-552, and VRC-16-667.

Female Hartley guinea pigs with body weights of 300 g each were purchased from Charles River Laboratories, MA. For each immunization, 400 μL of immunogen mix, containing 25 μg of specified, filter-sterilized protein immunogen and 80 μL of Adjuplex (Sigma-Aldrich Inc., MO, or Adjuplex equivalent formulated at VRC based on US patent No. 6,676,958 B2, Example 1) in PBS, was injected into the muscle of the two hind legs. While animals were under anesthesia, blood was collected through retro-orbital bleeding for serological analyses.

Female and male Indian-origin rhesus macaques with body weights of 2–9 kg were used for immunization studies. For each immunization, 1 mL of immunogen mix, containing 100 μg of specified, filter-sterilized protein immunogen and 200 μL of Adjuplex (Sigma-Aldrich Inc., MO, or Adjuplex equivalent formulated at VRC based on US patent No. 6,676,958 B2, Example 1) in PBS, was injected via a needle syringe into the caudal thighs of the two hind legs. Blood was collected 2 weeks postimmunization for serological analyses.


Fusion peptide ELISAs: Costar High Binding Half-Area 96-well plates (Corning, Kennebunk, ME) were coated with 50 µL/well of 2 µg/mL scaffold proteins in PBS overnight at 4 °C. Between steps, plates were washed five times with PBS-T (PBS + 0.05% Tween) and incubated at 37 °C for 1 h. After coating, plates were blocked with 100 μL/well of blocking buffer (B3T: 150 mM NaCl, 50 mM Tris-HCl, 1 mM EDTA, 3.3% FBS, 2% bovine albumin, 0.07% Tween 20, 0.02% thimerosal). Twofold serial dilution of 1:100 preimmunization and 1:1,000 postimmunization sera were used in the ELISA. Goat anti-mouse IgG (HRP-conjugated, GenScript) at 1:5,000 dilution was used for detection. Plates were developed with tetramethylbenzidine (TMB) substrate (SureBlue, KPL, Gaithersburg, MD) for 10 min before adding 1 N sulfuric acid (Fisher Chemical) to stop the reaction. Plates were read at 450 nm (Molecular Devices, SpectraMax using SoftMax Pro 5 software) and the optical densities (OD) were recorded.

BG505 SOSIP D7324 capture ELISAs: Costar High Binding Half-Area 96-well plates (Corning, Kennebunk, ME) were coated with 50 µL/well of 2 µg/mL of sheep D7324 antibody (AALTO Bio Reagents) in PBS overnight at 4 °C. Between steps, except for addition of trimer, plates were washed five times with PBS-T (PBS + 0.05% Tween) and incubated at room temperature (RT; 20–25 °C) for 1 h. After coating, plates were blocked with 100 μL/well of blocking buffer (5% skim milk, 2% bovine albumin, 0.1% Tween 20 in TBS). Next, 50 µL/well of 0.5 µg/mL D7324-tagged BG505.SOSIP trimer diluted in 10% FBS in PBS was added and incubated at RT for 2 h. Twofold serial dilution of 1:100 preimmunization and 1:1,000 postimmunization sera were used in the ELISA. Goat anti-mouse IgG (HRP-conjugated, GenScript) at 1:5,000 dilution was used for detection. Plates were developed with tetramethylbenzidine (TMB) substrate (SureBlue, KPL, Gaithersburg, MD) for 10 min before adding 1 N sulfuric acid (Fisher Chemical) to stop the reaction. Plates were read at 450 nm (Molecular Devices, SpectraMax using SoftMax Pro 5 software) and the optical densities (OD) were recorded. ELISA responses were plotted using PRISM (PRISM 7 GraphPad Software for Mac OS X).

Genetic assignment of antibodies

Antibody sequences were submitted to the ImMunoGeneTics information system (IMGT, http://www.imgt.org), subjected to variable (V), diverse (D), and joining (J) gene identification by alignment with the mouse germline sequences of the IMGT reference directory, and subject to IMGT/JunctionAnalysis for a detailed analysis of the V–J and V–D–J junctions. We only considered confirmed functional germline genes for the assigned germline. Clustal Omega software was used to prepare multiple-sequence alignments of antibody sequences for maximum-likelihood phylogenetic tree construction using the DNAML program in the PHYLIP package version 3.69 (http://evolution.genetics.washington.edu/phylip.html). Calculations were performed based on empirical base frequencies with transition/transversion (Ti/Tv) ratio of 2.0. Dendroscope 3 (dendroscope.org) was used to visualize phylogenetic trees64. The amino acid sequence alignments were visualized using BioEdit v7.2.5 editing software65. To calculate the minimum number of mutations required to switch between two different unmutated common ancestors, the unmutated common ancestor sequence was prepared by reverting the assigned V(D)J gene sequences into their corresponding germline sequences. Differences between unmutated common ancestor sequences were counted as the minimal mutation number required to switch from one unmutated common ancestor to another.

Antibody alanine/glycine scan

Binding of the vaccine elicited mouse vFP antibodies to 16 His-tagged fusion peptide (residues 512–521), including wild-type and alanine/glycine mutants, was assessed using a fortéBio Octet Red384 instrument. Briefly, the 16 peptides at 50 µg/mL in PBS were loaded onto Ni-NTA biosensors using their C-terminal histidine tags for 60 s. Typical capture levels were between 1.1 and 1.3 nm, and variability within a row of eight tips did not exceed 0.1 nm. These peptide-bound biosensors were equilibrated in PBS for 60 s followed by capture of the antigen binding fragments (Fabs, 250 nM) of the vaccine elicited vFP antibodies, VRC34.01, and an RSV F antibody (motavizumab) for 120 s and a subsequent dissociation step in PBS.

In all Octet measurements, parallel correction to subtract systematic baseline drift was carried out by subtracting the measurements recorded for a loaded sensor incubated in PBS. Data analysis was carried out using Octet software, version 9.0. The normalized responses obtained from one dataset or from a triplicate dataset were plotted using PRISM (PRISM 7 GraphPad software).

Surface plasmon resonance assay

Binding affinities and kinetics of antibodies to HIV-1 DS-SOSIP trimers and His-tagged fusion peptide were assessed by surface plasmon resonance on a Biacore T-200 (GE Healthcare) at 25 °C. To test antibody binding with HIV-1 DS-SOSIP trimers, 2G12 IgG was first immobilized on flow cells of a CM5 chip at ~3,000–8,000 response units. BG505 DS-SOSIP trimer and its glycan-deleted mutants, BG505 DS-SOSIP.∆88 and BG505 DS-SOSIP.∆611, at 500 nM in HBS-EP+ buffer (10 mM HEPES, pH 7.4, 150 mM NaCl, 3 mM EDTA, and 0.05% surfactant P-20) were then captured onto the 2G12 of one flow cell by flowing the protein solution over it for 60 s at a rate of 6 µL/min. Binding affinities for the 2G12-captured trimer were determined using a serial dilution of antibody Fab solutions, starting at 200 nM during the association phase. A dissociation phase at 30 µL/min for 300 s was used to determine binding kinetics. The surface was regenerated by flowing 3 M MgCl2 solution over it for 30 s at a flow rate of 50 µL/min. Blank sensorgrams were obtained injecting the same volume of HBS-EP+ buffer in place of the antibody Fab solution. Sensorgrams of the concentration series were corrected with corresponding blank curves and fitted globally with Biacore T200 evaluation software using a 1:1 Langmuir model of binding.

Affinity of antibody Fab to the His-tagged fusion peptide was measured on a Ni-NTA sensor chip (GE Healthcare). The Ni-NTA surface was activated by injection of 5 mM of Ni2SO4 in HBS-P+ buffer (10 mM HEPES, pH 7.4, 150 mM NaCl, and 0.05% surfactant P-20) for 60 s at 6 µL/min and then stabilized by washing with HBS-EP+ buffer containing 3 mM EDTA for 60 s at 30 µL/min. Fusion peptide with His-tag at 20 ng/mL was captured at 6 µL/min flow rate for 60 s over the nickel-activated sensor surface. Binding affinities for the 2G12-captured trimer were determined using a serial dilution of antibody Fab solutions starting at 200 nM during the association phase. A dissociation phase at 30 µL/min for 300 s was used to determine binding kinetics. The surface was regenerated by flowing 300 mM imidazole to both channels at 6 µL/min for 60 s. Sensorgrams of the concentration series were corrected with corresponding blank curves and fitted globally with Biacore T200 evaluation software using a 1:1 Langmuir model of binding.

HIV-1 Env mutagenesis

Site-directed mutagenesis on HIV-1 Env plasmids was performed through GeneImmune Biotechnology LLC, NY. T90A and S613A mutations were created to remove glycans 88 and 611, respectively.

HIV-1 Env-pseudotyped virus

293T-grown HIV-1 Env-pseudotyped virus stocks were generated by cotransfection of the wild-type or mutant Env expression plasmids with a pSG3ΔEnv backbone11.

Neutralization assays

A single round of entry neutralization assays using TZM-bl target cells were performed to assess monoclonal antibody neutralization as described11. Briefly, the monoclonal antibodies were tested via fivefold serial dilutions starting at up to 500 μg/mL. Monoclonal antibodies were mixed with the virus stocks in a total volume of 50 μL and incubated at 37 °C for 1 h. We then added 20 μL of TZM-bl cells (0.5 million/mL) to the mixture and incubated it at 37 °C overnight. On day 2, 130 μL cDMEM were added, and cells were lysed on day 3 and assessed for luciferase activity (RLU). The 50% and 80% inhibitory concentrations (IC50 and IC80) were determined using a hill-slope regression analysis as described11.

To assess monoclonal antibody neutralization on a panel of 208 HIV-1 Env-pseudotyped viruses, an automated 384-well microneutralization assay was performed as described previously66.

Serum neutralization was also assessed in the single round of entry neutralization assays using TZM-bl target cells, as described above. Before evaluation, all sera from immunized and control animal were heat-inactivated at 56 °C for 1 h. All sera were tested via fourfold serial dilutions starting at 1:20 dilution.

Serum neutralization with FP competition was performed with serum in presence of either PEGylated FP9 (AVGIGAVFL) or PEGylated noncognate FLAG peptide. Mean and s.d. of results from triplicated experiments were determined.

Protein complex preparation

Antibody Fab and fusion peptide (residues 512–518) complexes were prepared by first dissolving fusion peptide in 100% DMSO at 50 mg/mL concentration, then mixing it with Fab solution in a 10:1 molar ratio to reach a final protein complex centration of 15 mg/mL.

Protein crystal screening

Antibody Fab and fusion peptide (residues 512–518) complexes were screened for crystallization in JCSG1-4 protein-crystal screening kits using a Cartesian Honeybee crystallization robot, as described previously15, and a mosquito robot. Crystals initially observed from the wells were manually reproduced. The vFP1.01/FP complex crystal grew in 0.2 M AmSO4 and 0.1 M NaOAc, pH 4.6; the vFP7.04/FP complex crystal grew in 0.1 M MES, pH 6.0, 30% PEG 6000; the vFP16.02/FP complex crystal grew in 0.1 M NaOAc, pH 4.5, and 2 M AmSO4; the vFP20.01/FP complex crystal grew in 0.1 M citric acid, pH 3.5, ad 2 M AmSO4; and the vFP5.01/FP complex crystals grew in 0.2 M MgCl2, 0.1 M Tris-HCl, pH 8.5, and 20% PEG 8000.

X-ray data collection, structure solution, model building, and refinement

Crystals were cryoprotected in 20% glycerol and flash-frozen in liquid nitrogen. Data were collected at a temperature of 100 K and a wavelength of 1.00 Å at the SER-CAT beamline ID-22 (Advanced Photon Source, Argonne National Laboratory). Diffraction data were processed with the HKL2000 suite67. Structure solution was obtained by molecular replacement with Phaser using homologous Fab structures (PDB IDs: 3BKY for vFP1-class antibody complex and 3LEY for vFP5.01 antibody complex) as search models. Model building was carried out with Coot68. Refinement was carried out with Phenix69. Ramachandran statistical analysis indicated that the final structures contained no disallowed residues or no more than 0.23% disallowed residues. Data collection and refinement statistics are shown in Supplementary Table 4.

Cryo-EM data collection and processing

The Env trimer used in cryo-EM was generated in the GNTI– cell line as described previously41. To prepare Env complexes, BG505 DS-SOSIP at a final concentration of 0.3–0.5 mg/mL was incubated with four- to fivefold molar excess of the antibody Fab fragments for 30–60 min. To prevent aggregation during vitrification, the sample was incubated in 0.085 mM n-dodecyl β-D-maltoside (DDM). The vFP1.01 and vFP5.01 bound complexes were vitrified by applying 3 μL of sample to freshly plasma-cleaned C-flat holey carbon grids (CF-1.2/1.3-4C; EMS, Hatfield, PA) for vFP1.01 and gold grids for vFP5.01, allowing the sample to adsorb to the grid for 60 s, followed by blotting with filter paper and plunge-freezing into liquid ethane using the CP3 cryo-plunger (Gatan, Inc.; 20 °C, 85–90% relative humidity).

The vFP16.02 and vFP20.01 bound complexes were vitrified using a semiautomated Spotiton V1.0 robot70,71 The grids used were specially designed Nanowire self-blotting grids with a carbon lacey supporting substrate72. Sample was dispensed onto these nanowire grids using a picoliter piezo dispensing head. A total of ~5 nL sample was dispensed in a stripe across each grid, followed by a pause of a few milliseconds before the grid was plunged into liquid ethane.

Data were acquired using the Leginon system installed on a Titan Krios electron microscopes operating at 300 kV and fitted with a Gatan K2 Summit direct detection device. The dose was fractionated over 50 raw frames and collected over a 10-s exposure time. Individual frames were aligned and dose-weighted using MotionCor273.

CTF was estimated using the GCTF package74. Particles were picked using DoG Picker within the Appion pipeline75. 2D and 3D classifications were performed using RELION76. A map of unliganded BG505 SOSIP.664 (EMDB ID EMD-5782), lowpass-filtered to 60 Å, was used as the starting point of 3D classification, followed by 3D refinement in either RELION or cryoSparc77. For the vFP16.02 and vFP20.01 complexes, after 3D classification in RELION, an additional step of ab initio reconstruction was performed using cryoSparc.

Cryo-EM model fitting

Fits of HIV-1 trimer and Fab to the cryo-EM reconstructed maps were performed using Chimera78. Glycosylated BG505 SOSIP trimer structure (PDB ID: 5FYL) was used for the trimer fits. For antibody fitting, we used the fusion peptide-bound coordinates of vFP1.01 and vFP5.01. For the antibody Fabs, both orientations (rotated ~180° about the Fab longitudinal axis) were tested, and the optimal fit was decided based on map-to-model correlation and positioning of the fusion peptide bound to the Fab relative to Env. For the vFP16.02 and vFP20.01 bound complexes, the coordinates were further fit to the electron density by an iterative process of manual fitting using Coot68 and real space refinement within Phenix69. Molprobity79 and EMRinger80 were used to check geometry and evaluate structures at each iteration step. Figs. were generated in UCSF Chimera and PyMOL. Map-fitting cross correlations were calculated using the Fit-in-Map feature in UCSF Chimera. Map-to-model FSC curves were generated using EMAN2. Local resolution of cryo-EM maps was determined using RELION.

Defining vFP1-class antibody V-gene sequence signature

The V-gene sequence signatures for vFP1 class antibodies were defined by examining the vFP1 class antibody sequences that neutralize at least seven of the ten tested strains and the structures of FP in complex with vFP1.01, vFP16.02, and vFP20.01. A residue position was considered part of the sequence signature if at least one side-chain heavy atom was within 5 Å of any fusion peptide heavy atom for all three complex structures, no more than three similar amino acid types had a combined prevalence of more than 90%, and each of these amino acid types had a prevalence of more than 10%.

Molecular dynamics simulation of mannose-5 Env trimer

By using the BG505 SOSIP.664 Env trimer structure (PDB ID: 4TVP) as a starting template, we modeled in a fully extended mannose-5 moiety at each N-linked glycosylation sequon. The fusion peptide structure was then grafted onto our full mannose-5 model followed by 5,000 steps of conjugate gradient energy minimization in implicit solvent using NAMD. The obtained structure was then solvated in a 17-Å padding water box, neutralized by the addition of NaCl at a concentration of 150 mM. The CHARMM force field (https://www.charmm.org) was used to parameterize the protein (including CMAP corrections and mannose-9). TIP3P water parameterization81 was used to describe the water molecules.

Two independent molecular simulations were carried out using ACEMD molecular dynamics software on their METROCUBO workstation (https://www.acellera.com/products/GPU-hardware-molecular-dynamics-metrocubo/). The system was minimized for 2,000 steps, followed by equilibration using the NPT ensemble for 50 ns at 1 atm and 300 K using a timestep of 2 fs. We also used rigid bonds and a 9-Å cutoff using PME for long range electrostatics. During the equilibration phase, heavy atoms on the protein were constrained by a 1 kcal/molÅ2 spring constant and slowly relaxed over the first 5 ns. Following the relaxation phase, the protein was allowed to move freely and simulated for 500 ns under the NVT ensemble using ACEMD's NVT ensemble with a Langevin thermostat. To achieve a timestep of 4 ps, we used damping at 0.1 ps –1 and a hydrogen mass repartitioning scheme. Each simulation ran up to 500 ns.

Conformations of the fusion peptide (residues 512–519) were extracted from the MD simulations every 100 ps, producing an ensemble of 30,000 structures. Prody (http://prody.csb.pitt.edu) was used to perform the principal component analysis of backbone atoms. The conformations of five crystalized fusion peptides were then projected into the eigenspace defined by the first two components: vFP1.01, vF5.01, PGT151 (PDB: 5FUU), VRC34.01 (PDB: 5I8H) and clade G (PDB: 5FYJ).

Analysis of antibody angle of approach to HIV-1 Env

To compare modes of antibody recognition of HIV-1 Env by vaccine-elicited fusion peptide antibodies and VRC34.01, structural models of antibody in complex with HIV-1 BG505 SOSIP Env trimer derived from X-ray crystallography and EM were superimposed by pairwise alignment of the Cα atom coordinates of the HIV-1 Env. To simplify the comparison, we first defined two common axes on the HIV-1 Env, the trimer axis and the protomer axis, as reference lines. The trimer axis was defined by two points, each with x, y, z coordinates obtained by averaging the coordinates of the Cα atom of a residue and its threefold symmetry mates on the same trimer. The protomer axis was defined by a line perpendicular to the trimer axis and that passes through the center of the protomer. On the antibody side, we also defined two axes for each Fab. The long axis of a Fab was defined by two points, one point from the variable domain with x, y, z coordinates obtained by averaging the coordinates of the Cα atom of the four conserved Cys (Cys 22 and Cys92 of heavy chain, and Cys23 and Cys88 of light chain), and the other point from the constant domain with x, y, z coordinates obtained by averaging the coordinates of the Cα atom of the four conserved Cys (Cys 140 and Cys196 of heavy chain, and Cys134 and Cys194 of light chain). The short axis of a Fab was defined by a line connecting Cα atoms of heavy chain Cys22 and light chain Cys23. Approaching angles of each antibody were then calculated as (i) angle between trimer axis and Fab long axis, and (ii) angle between the axis of major interacting protomer and Fab long axis. In addition, the angles between Fab variable domains were defined by the angles of their short axes. The axes were visualized in PyMOL by placing their coordinates in a PDB file.

Autoreactivity assay

Antibodies were assessed for autoreactivity by testing for binding to HEp2 cells by indirect immunofluorescence (Zeus Scientific, ANA HEp2 test system) and cardiolipin by ELISA (Inova Diagnostics, QUANTA Lite ACA IgG III), per the manufacturers’ instructions. On HEp2 cells, antibodies were assigned a score between 0 and 3+, using control antibodies as reference. In the cardiolipin binding assay, OD values were converted to GPLs using standard samples provided in the kit. Monoclonal antibodies that scored greater than 20 GPLs at 33 µg/mL were considered autoreactive.

Neutralization fingerprinting analysis

The neutralization fingerprint of a monoclonal antibody or polyclonal plasma is defined as the potency pattern with which the antibody/plasma neutralizes a set of diverse viral strains. The neutralization fingerprints of a set of monoclonal antibodies and NHP plasma were compared and clustered according to fingerprint similarity, as described previously82. A set of 132 strains83 was used in the neutralization fingerprint analysis for Supplementary Fig. 11, and the 58 FP-selected strains were used for Fig. 6.

Associations between glycosylation patterns versus neutralization

We calculated the associations between the sequence variability of FP-neighboring glycosylation sites (HXB2 numbering 88, 241, 448, and 611) and large-panel neutralization using an approach implemented with R package SeqFeatR (https://seqfeatr.zmb.uni-due.de). Briefly, for each residue position we created contingency table based on glycan occurrence and neutralization sensitivity and evaluated the association using Fisher's exact test. The resulting P values were corrected using Holm's multiple testing method.

Statistical analysis

The correlation between neutralization breadth on the 58-strain panel with FP8 = AVGIGAVF and neutralization breadth on the full 208-strain panel was performed using Pearson correlation. The differences in number of neutralized strains between the FP-KLH-primed + DS-SOSIP-boosted group and the DS-SOSIP-alone group were evaluated using one-tailed Mann–Whitney tests. The differences in neutralization between FP-KLH groups and the KLH-only group were evaluated using one-tailed Mann–Whitney tests. The correlation between antibody trimer binding and antibody neutralization breadth was performed using Pearson correlation. The differences in divergence of germline between antibodies from trimer-primed groups and antibodies from non-trimer-primed groups were evaluated using two-tailed Mann–Whitney tests. The differences in sera neutralization between trimer-boosted animals and non-trimer-boosted animals were evaluated using one-tailed Mann–Whitney tests. The association of FP-proximal N-glycan sequons (N88, N241, N448, and N611) and neutralization based on the 208-strain panel was evaluated using two-tailed Fisher's exact tests. Unless otherwise indicated, all data were plotted and graphed using GraphPad Prism, version 7.0; and P < 0.05 indicated a statistically significant difference.

Reporting Summary

Further information on experimental design is available in the Nature Research Reporting Summary linked to this article.

Code availability

No studies deemed central to the conclusions were carried out with custom code.

Data availability

All data generated or analyzed during this study are included in this published article (and its Supplementary Information files). Atomic coordinates and structure factors of the reported crystal structures were deposited in the Protein Data Bank with PDB IDs 5TKJ, 5TKK, 6CDM, 6CDO, 6CDP. Cryo-EM reconstructions were deposited in the Electron Microscopy Data Bank with EMDB accession codes EMD-7460, EMD-7459, EMD-8420, EMD-8421, and EMD-8422, and in Protein Data Bank with PDB ID 6CDI and 6CDE. Heavy chain- and light chain-variable sequences of monoclonal antibodies vFP1.01–vFP7.05 and vFP7.06–vFP 32.07 were deposited with GenBank under accession numbers KX949064KX949087 and MH017667MH017826, respectively.

Additional information

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We thank J. Chrzas, U. Chinte, Z. Jin, and staff at SER-CAT (Southeast Regional Collaborative Access Team) for help with X-ray diffraction data collection; B. DeKosky for suggestions on lineage discrimination, W. Rice and SEMC staff for assistance with cryo-EM data collection; and J. Stuckey for assistance with figures. We thank D. Burton and M. Fineberg (International AIDS Vaccine Initiative (IAVI), Neutralizing Antibody Consortium (NAC)) for antibodies, including PGT122 used in cryo-EM studies, B. Haynes (The Duke Center for HIV/AIDS Vaccine Immunology and Immunogen Discovery (CHAVI-ID)) for information on antibody CH07, R. Sanders (Academisch Medisch Centrum Universiteit van Amsterdam (AMC)) for information on antibody ACS202, B. Graham (Vaccine Research Center, NIAID, NIH) for murine antibody 5C4, and the WCMC/AMC/TSRI HIVRAD team for their contributions to the design and validation of near-native mimicry for soluble BG505 SOSIP.664 trimers. We thank members of the Structural Biology Section, Structural Bioinformatics Core Section, and Human Immunology Section of the Vaccine Research Center for helpful comments. Support for this work was provided by the Intramural Research Program of the Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health. This work was also supported in part by IAVI's NAC (J.R.M and P.D.K.) and with federal funds from the Frederick National Laboratory for Cancer Research, NIH, under contract HHSN261200800001E (Y.T.). I.S.G. received support from NIH grant R01 AI131722. Some of this work was performed at the Simons Electron Microscopy Center and National Resource for Automated Molecular Microscopy, located at the New York Structural Biology Center, supported by grants from the Simons Foundation (SF349247) NYSTAR, and the NIH National Institute of General Medical Sciences (GM103310), with additional support from Agouron Institute (F00316) and NIH (OD019994). Use of insertion device 22 (SER-CAT) at the Advanced Photon Source was supported by the US Department of Energy, Basic Energy Sciences, Office of Science, under contract W-31-109-Eng-38.

Author information

Author notes

  1. These authors contributed equally: Kai Xu, Priyamvada Acharya, Rui Kong, Cheng Cheng.


  1. Vaccine Research Center, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Bethesda, MD, USA

    • Kai Xu
    • , Priyamvada Acharya
    • , Rui Kong
    • , Cheng Cheng
    • , Gwo-Yu Chuang
    • , Kevin Liu
    • , Mark K. Louder
    • , Sijy O’Dell
    • , Reda Rawi
    • , Mallika Sastry
    • , Chen-Hsiang Shen
    • , Baoshan Zhang
    • , Tongqing Zhou
    • , Mangaiarkarasi Asokan
    • , Robert T. Bailer
    • , Michael Chambers
    • , Xuejun Chen
    • , Chang W. Choi
    • , Nicole A. Doria-Rose
    • , Aliaksandr Druz
    • , S. Katie Farney
    • , Kathryn E. Foulds
    • , Hui Geng
    • , Jason Gorman
    • , Kurt R. Hill
    • , Alexander J. Jafari
    • , Young D. Kwon
    • , Yen-Ting Lai
    • , Krisha McKee
    • , Tiffany Y. Ohr
    • , Li Ou
    • , Dongjun Peng
    • , Ariana P. Rowshan
    • , John-Paul Todd
    • , Elise G. Viox
    • , Yiran Wang
    • , Yongping Yang
    • , Amy F. Zhou
    • , Diana G. Scorpio
    • , Adrian B. McDermott
    • , Lawrence Shapiro
    • , John R. Mascola
    •  & Peter D. Kwong
  2. National Resource for Automated Molecular Microscopy, Simons Electron Microscopy Center, New York Structural Biology Center, New York, NY, USA

    • Priyamvada Acharya
    • , Venkata P. Dandey
    • , Edward T. Eng
    • , Hui Wei
    • , Bridget Carragher
    •  & Clinton S. Potter
  3. Vanderbilt Vaccine Center, Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, and Department of Electrical Engineering and Computer Science, Vanderbilt University, Nashville, TN, USA

    • Ivelin S. Georgiev
  4. Department of Pharmaceutical Chemistry, University of California San Francisco, San Francisco, CA, USA

    • Thomas Lemmin
  5. Department of Biochemistry and Molecular Biophysics, Columbia University, New York, NY, USA

    • Zizhang Sheng
    • , Lawrence Shapiro
    •  & Peter D. Kwong
  6. Department of Systems Biology, Columbia University, New York, NY, USA

    • Zizhang Sheng
    •  & Lawrence Shapiro
  7. Electron Microscopy Laboratory, Cancer Research Technology Program, Leidos Biomedical Research, Inc., Frederick National Laboratory for Cancer Research, Frederick, MD, USA

    • Yaroslav Tsybovsky
  8. GenScript USA, Piscataway, NJ, USA

    • Rui Chen
    •  & Lu Yang


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K.X. conceived and led the project and determined crystal structures; P.A. determined cryo-EM structures; R.K. and N.A.D.-R. coordinated neutralization assessments; C.C. coordinated guinea pig and NHP immunization; G.-Y.C. coordinated statistical and bioinformatical analyses; K.L. prepared proteins and co-determined crystal structures; M.K.L. and R.T.B. assessed antibody neutralization in the large panel; C.-H.S. performed antibody sequence analyses; M.S. performed all Alanine–Glycine scans; B.Z. prepared antibodies for the large panel and performed various binding analyses; T.Z. performed SPR analyses, calculated the antibody's approach angle to the trimer, and made antibody neutralization dendrograms; M.A. performed antibody autoreactivity tests; I.S.G. performed antibody neutralization fingerprint analyses; T.L. performed molecular dynamics analyses; S.O’D., K.M., C.W.C., E.G.V., and A.P.R. co-performed neutralization assays; A.D., D.P., B.Z., and Y.Y. helped with protein expression; E.T.E., V.P.D., and H.W. helped with cryo-EM structures; X.C., H.G., J.G., M.S., and Y.D.K. performed protein purification; K.R.H., A.J.J., K.E.F., D.G.S., and J.-P.T. assisted in the NHP study; Y.-T.L. and Y.W. assisted with X-ray crystal dataset processing; B.Z., L.O., and M.C. helped with immunogen preparation and characterization; R.R. and S.K.F. performed statistical and bioinformatical analyses; Z.S. performed antibody gene comparisons; Y.T. performed negative-stain EM; T.Y.O. participated in immunogen binding tests; A.F.Z. helped with SPR assays; R.C. and L.Y. supervised the research team in GenScript; A.B.M. supervised MSD-based immunogen antigenicity characterization; L.S. supervised antibody gene analyses and comparison; B.C. and C.S.P. supervised cryo-EM studies; K.X., L.S., J.R.M., and P.D.K. wrote the manuscript; and all authors read, edited, and approved the manuscript. J.R.M. and P.D.K. conceived and supervised the study.

Competing interests

The authors declare no competing financial interests.

Corresponding authors

Correspondence to John R. Mascola or Peter D. Kwong.

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