Skip to main content

Thank you for visiting You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

The structures of two archaeal type IV pili illuminate evolutionary relationships


We have determined the cryo-electron microscopic (cryo-EM) structures of two archaeal type IV pili (T4P), from Pyrobaculum arsenaticum and Saccharolobus solfataricus, at 3.8 Å and 3.4 Å resolution, respectively. This triples the number of high resolution archaeal T4P structures, and allows us to pinpoint the evolutionary divergence of bacterial T4P, archaeal T4P and archaeal flagellar filaments. We suggest that extensive glycosylation previously observed in T4P of Sulfolobus islandicus is a response to an acidic environment, as at even higher temperatures in a neutral environment much less glycosylation is present for Pyrobaculum than for Sulfolobus and Saccharolobus pili. Consequently, the Pyrobaculum filaments do not display the remarkable stability of the Sulfolobus filaments in vitro. We identify the Saccharolobus and Pyrobaculum T4P as host receptors recognized by rudivirus SSRV1 and tristromavirus PFV2, respectively. Our results illuminate the evolutionary relationships among bacterial and archaeal T4P filaments and provide insights into archaeal virus-host interactions.


It has been recognized for many years that bacterial type IV pili (T4P)1,2, important in activities such as adhesion3,4, twitching motility5, surface-sensing6 and natural transformation7, are homologs of two different classes of archaeal surface structure, pili and flagellar filaments8,9,10,11. The archaeal flagellar filament is a unique rotating T4P-like assembly which enables motility and is conserved in widely different archaeal lineages, including hyperthermophiles, halophiles and methanogens12. Archaeal T4P are even more widespread and functionally diverse13. Although the full spectrum of functions played by archaeal T4P is yet to be uncovered, they are known to mediate adhesion to various biotic and abiotic surfaces, and play an important role in DNA exchange, intercellular communication and biofilm formation14,15. Furthermore, T4P serve as receptors for certain hyperthermophilic archaeal viruses, including Sulfolobus islandicus rod-shaped viruses 2 and 8 (SIRV2 and SIRV8, respectively; family Rudiviridae)16,17 and Sulfolobus turreted icosahedral virus (STIV; family Turriviridae)18.

Despite the importance of bacterial and archaeal T4P-like filaments, the structural details of these filaments remain sparse. However, the revolution in cryo-EM has now led to atomic structures for seven bacterial T4P19,20,21, three archaeal flagellar filaments22,23,24, one archaeal “flagellar-like” filament25, and one archaeal T4P26. Interestingly, a 4.1-Å resolution structure of the T4P from S. islandicus, a hyperthermophilic and acidophilic crenarchaeon, revealed an unprecedented level of O-glycosylation on this filament26. The adhesive pilus displayed an anomalous amino acid composition, with 37% of the residues in the C-terminal globular domain being threonines and serines, most of which are exposed and likely glycosylated on the surface of the filament. The core of the filament was, as expected, extremely hydrophobic, since the N-terminal domains that constitute the core are transmembrane helices prior to filament assembly. However, the overall percentage of charged residues within the entire pilin protein was only 1.5%. Remarkably, the S. islandicus pilus was found to be extremely resilient under various harsh conditions, including extended treatment with different proteases and even boiling in 5 M guanidine hydrochloride. The reason for the robustness of the pilus was attributed to a combination of profound hydrophobicity and extensive surface glycosylation of the filament26. Notably, the resilience of the S. islandicus pilus precluded the identification of the constituent pilin protein using conventional approaches, such as gel electrophoresis and mass spectrometry. Instead, the identity of the protein was determined using a combination of cryo-EM and bioinformatics, whereby candidate protein sequences were directly threaded through the density maps, which allowed building an atomic model de novo, exemplifying the power of cryo-EM for protein identification26.

Whether T4P of other hyperthermophilic archaea display similar sequence features and properties as those described for S. islandicus pilus remains unclear. Indeed, the existence of a single atomic structure for an archaeal T4P has limited generalizations about such filaments as well as comparisons with homologs. We present in this paper the structure of two additional archaeal T4P, one from Pyrobaculum arsenaticum, a neutrophilic hyperthermophile (optimal growth at 90 °C, pH 7) and the other from Saccharolobus solfataricus, an acidophilic hyperthermophile (optimal growth at 75–80 °C, pH 2-3). We use the three structures of archaeal T4P to make comparisons with bacterial T4P and archaeal flagellar filaments. We show that whereas the N-terminal domain is conserved in all bacterial and archaeal T4P-like filaments, the C-terminal domain of bacterial T4P is unrelated to the immunoglobulin (Ig)-like domain shared by archaeal T4P and archaeal flagella. Furthermore, comparison of the pili from the acidophilic and neutrophilic hyperthermophiles suggests that extensive glycosylation is a response to an acidic environment, rather than simply high temperature. Notably, the pili of Pyrobaculum are much less glycosylated compared to the Sulfolobus and Saccharolobus pili, and as a consequence, the Pyrobaculum filaments do not display the remarkable stability of the Sulfolobus filaments in vitro. Finally, we show that Pyrobaculum and the Saccharolobus T4P are at the forefront of virus-host interaction and are recognized by two different viruses, likely serving as primary receptors during virus infection.


Archael viruses bind to pili

We have recently isolated two filamentous viruses, Saccharolobus solfataricus rod-shaped virus 1 (SSRV1; family Rudiviridae) and Pyrobaculum filamentous virus 2 (PFV2; family Tristromaviridae), infecting Saccharolobus solfataricus POZ149 and Pyrobaculum arsenaticum 2GA, respectively27,28. After centrifugation in CsCl density gradient, both viruses co-purify with and are often bound with their terminal fibers to host-derived pili-like filaments, which were ~80 Å in diameter (Fig. 1a, b). Consequently, the filaments appear to serve as the primary receptors for SSRV1 and PFV2, as has been demonstrated for some other archaeal viruses16,17,18.

Fig. 1: Cryo-EM of the P. arsenaticum pilus and the S. solfataricus pilus.
figure 1

Representative cryo-electron (a) and negative staining (b) micrographs of the P. arsenaticum pili interacting with filamentous virus PFV2. Scale bar, 20 nm in a and 200 nm in b. Orange arrowhead points to the P. arsenaticum pilus; blue arrowhead points to the PFV2 virion; green arrow points to the regions of the pilus-virion interaction. Representative cryo-electron (c) and negative staining (d) micrographs of the S. solfataricus pili interacted with filamentous virus SSRV1. Scale bar, 20 nm in c and 200 nm in d. Orange arrowhead points to the S. solfataricus pilus; blue arrowhead points to the SSRV1 virion; green arrow points to the regions of the pilus-virion interaction. Cryo-EM reconstruction of the P. arsenaticum pilus at 3.8 Å resolution (e) and the S. solfataricus pilus at 3.4 Å resolution (f). Thin slices parallel to the helical axis of the pilus are shown, colored by the helical radius. g, h Side view and top view of the P. arsenaticum and S. solfataricus pilus atomic models, built into the cryo-EM maps shown in e, f. The model is colored by chain. Helical net of the pilus (P. arsenaticum pilus in i and the S. solfataricus pilus in j) using the convention that the surface is unrolled and we are viewing from the outside.

Cryo-EM structures of two archaeal pili

In the absence of genetic tools for S. solfataricus POZ149 and P. arsenaticum 2GA, we set out to determine the identity of the SSRV1 and PFV2 host receptors directly by cryo-EM, applying the strategy recently employed for identification of the S. islandicus pilin26. To this end, mixtures of virions and pili-like filaments were imaged by cryo-EM separately for SSRV1 and PFV2, respectively, and the images of the pili were used for three-dimensional reconstruction. While multiple helical symmetries appeared to be possible based upon analysis of power spectra from these filaments29, in each case only one helical symmetry led to a reconstruction with clearly interpretable secondary structure. This was a rise of ~5.3 Å and a rotation of ~101.7° for the P. arsenaticum filaments and a rise of ~5.0 Å and a rotation of ~104.6° for the S. solfataricus filaments (Table 1). The small difference in helical twist between the two resulted in 7-start long-pitch helices that were left-handed for P. arsenaticum (Fig. 1e, i) and right-handed for S. solfataricus (Fig. 1f, j). The 7-start helices arise from the fact that there are ~3.5 subunits per turn of the right-handed 1-start helix in both filaments. However, in P. arsenaticum pilus, there are slightly more than 3.5 subunits per turn, so there are 7.1 subunits in two turns, while in S. solfataricus there are slightly less than 3.5 subunits per turn, yielding 6.9 subunits in two turns. The reconstructions had a resolution of 3.8 Å for P. arsenaticum pilus and 3.4 Å for S. solfataricus pilus, as judged by a map:map Fourier shell correlation (FSC), a map:model FSC as well as d9930 (Supplementary Fig. 1, Table 1).

Table 1 Cryo-EM and refinement statistics of the P. arsenaticum and the S. solfataricus pilus.

Hyperthermophilic archaea typically carry multiple pilin genes13. Thus, to identify the exact pilin genes encoding receptors of SSRV1 and PFV2, we have sequenced the complete genomes of S. solfataricus POZ149 and P. arsenaticum 2GA (see Methods), and used a combination of mass spectrometry, bioinformatics, and cryo-EM to build de novo the atomic models (Fig. 2a, b), as was done for the pili from S. islandicus26. The result in each case was finding a single protein sequence that could be threaded through the maps, which is HC235_07175 for P. arsenaticum (Par_PilA) and HFC64_06120 for S. solfataricus (Sso_PilA) (Supplementary Figs. 2, 3). Our structural models indicate that the first 12 residues in Sso_PilA and 7 residues in Par_PilA correspond to the signal sequence, which is cleaved from the mature pilin protein. In Sso_PilA, cleavage occurs between the Gly12 and Leu13 residues (Supplementary Fig. 2d) and the cleavage site matches perfectly with the previously established11 consensus recognition motif of the signal peptidase PibD ((Lys/Arg)-(Gly/Ala)-↓-(Leu/Ile/Phe)-(Ser/Thr/Ala)). In contrast, in Par_PilA, cleavage occurs between residues Gly7 and Met8 of the prepilin, and the PibD cleavage site (Arg-Gly↓Met-Thr) slightly deviates from the consensus motif (Supplementary Fig. 2c). BLASTP searches have shown that orthologs of Sso_PilA are conserved in other members of the order Sulfolobales, including different species of the genera Saccharolobus, Sulfolobus, Acidianus and others. Similarly, Par_PilA pilins are conserved in Pyrobaculum species. Notably, in a number of Pyrobaculum genomes, the orthologs of Par_PilA appear to be misannotated, with the second Met codon (corresponding to Met8 of Par_PilA prepilin) selected as the start codon; as a result, these proteins appear to lack the signal sequence.

Fig. 2: Two-domain architecture of archaeal type IV pilus (T4P).
figure 2

Protein Cα trace of a single P. arsenaticum pilin (a) and S. solfataricus pilin (b). Pilin structures are shown in cartoon, colored by secondary structure. The map quality of the N-terminal long helix and C-terminal globular domain are shown on the right. c Structure-based sequence alignments of three archaeal type IV pilins with known structures, P. arsenaticum pilin, S. solfataricus pilin and previously determined S. islandicus pilin. Sequences were aligned using Tcoffee67 and visualized with Jalview68. The two blue shades correspond to the amount of sequence identity (dark blue when all three are identical, light blue when two are identical). The observed glycosylated residues are indicated with stars: solid red stars for O-linked sugars in S. solfataricus, open red stars for O-linked sugars in S. islandicus, and a blue star for N-linked sugar in P. arsenaticum. The blue line above the star indicates the NxS/T motif associated with N-linked glycosylation in P. arsenaticum. Two cysteine residues that form a disulfide bond in P. arsenaticum are indicated with yellow lock symbols. Note that amino acid positions are counted starting with the first amino acid of the mature protein (i.e., following cleavage of the signal peptide). d Superposition of a single P. arsenaticum pilin (purple) and S. solfataricus pilin (cyan), aligned by either the globular domain (left) or the N-terminal helix (right). e Flexible secondary structure alignment reveals a simple mapping of the local secondary structure elements between the two pilins. The N-terminal domain is α-helical, and each β-strand in the C-terminal domain is shown as a closed shape. f The C-terminal loop of the P. arsenaticum pilin and the disulfide bond.

The S. solfataricus pilus was very similar to that of S. islandicus, albeit at considerably higher resolution (3.4 versus 4.1 Å), which was not surprising given the ~81% sequence identity between the two. In contrast, the sequence identity between the pilins from P. arsenaticum and S. solfataricus is only ~18% (Fig. 2c). The structural comparison between the two pilins (Fig. 2d) reveals that, even with low sequence identity, both the N-terminal and C-terminal domains are structurally conserved. They both have the archaeal T4P two-domain fold described for the S. islandicus LAL14/1 pilus26, containing a ~35 amino acid-long N-terminal α-helical domain and C-terminal globular Ig-like β-sandwich domain. In fact, there is nearly a one-to-one mapping of secondary structural elements between the two (Fig. 2e), with the exception that one β-strand in P. arsenaticum (residues 36–46) maps to two shorter β-strands in S. solfataricus. However, the relative orientation of these two domains is different by ~40° (Fig. 2d) and, as a result, the helical packing in the filaments is different (Fig. 1g, h). Interestingly, and in contrast to the S. islandicus and S. solfataricus pilins, P. arsenaticum pilin has a 15 amino acid C-terminal extension that wraps around the globular domain. Within this extension, an intramolecular disulfide bond is formed between Cys139 in the extension and Cys80 within the same pilin chain (Fig. 2f, Supplementary Fig. 4), which is likely to contribute to the thermo-stability of this pilus.

Glycosylation of the pili

Despite high sequence similarity between the pilins of S. islandicus and S. solfataricus, SSRV1 does not bind to S. islandicus pili and, accordingly, cannot infect this organism27. Given that the surface of the S. islandicus pilus is coated with a glycan layer26, the latter might play an important, if not key, role in virus binding. Thus, we next analyzed the glycosylation status of the S. solfataricus and P. arsenaticum pili. It turned out that amino acid distributions and glycosylation represent the most striking differences between the two pilins (Supplementary Table 1). In the S. solfataricus pilin, similar to S. islandicus, only about 1.5% of the residues are charged. We showed26 that extensive glycosylation makes these extremely hydrophobic filaments soluble. In contrast, ~10% of the residues in P. arsenaticum pilin are charged. In S. solfataricus and S. islandicus, ~37% of the residues in the globular domain are either serine or threonine, potential sites for O-linked glycosylation. In P. arsenaticum pilin as well as archaeal flagella and adhesion filaments22,23,24,25,26, only ~20% of the residues are serine or threonine (Fig. 3a). No extra density corresponding to O-linked glycosylation was reported, except for one serine in the flagellar filament of M. hungatei22. In S. solfataricus, we see clear extra density consistent with glycosylation on seven residues, all serines or threonines (Fig. 3b). In contrast, in P. arsenaticum only a single density consistent with glycosylation is seen, on Asn55 (Fig. 3b), which would be N-linked glycosylation.

Fig. 3: Glycosylation of archaeal type IV pilus and other archaeal cell appendages.
figure 3

a Violin plot showing the distributions of the serine and threonine percentages in all proteins of M. hungatei, M. maripaludis, P. furiosus, I. hospitalis, P. arsenaticum, S. solfataricus and S. islandicus. The red diamond indicates the percentage of serine+threonine in the pilin or flagellin from this species discussed in this paper. The black box indicates the interquartile range, and the central line in the box indicates the median of the data. The species for the archaeal flagellar filaments are colored in blue-ish colors, adhesion filaments in orange, and archaeal T4P in green-ish colors. b Density (magenta) due to post-translational modifications on P. arsenaticum pilin (left) and S. solfataricus pilin (right). The protein Cα backbone is colored in orange (P. arsenaticum) or yellow (S. solfataricus). The extra density is due to N-linked (Asn) or O-linked (Thr, Ser) sugars, and the residues modified are labeled. c Surface glycosylation of the P. arsenaticum pilus (left), S. solfataricus pilus (middle) and a control rod-like virus without apparent glycosylation. The control virus and the S. solfataricus pilus were purified and imaged together. All three volumes were filtered to 7 Å. The density accounted for by atomic models is colored in gray, and the extra density is colored in magenta. Three different display thresholds are shown. A small additional density appears on the surface of the virus, and this is due to several C-terminal residues that were not part of the atomic model due to disorder, and not due to glycosylation.

We expect that most glycosylation is not seen in the high-resolution maps due to the disorder of the sugars, and the fact that the same residue may not be glycosylated in every subunit. However, we can directly visualize at lower resolution additional mass consistent with glycosylation (Fig. 3c) by subtracting the predicted density due to the atomic model from the actual maps, after both are filtered to 7 Å. We are fortunate to have a control for this procedure which involves the rod-shaped virus SSRV1 present in the images for the S. solfataricus pili. There was no apparent glycosylation of this virus, and the small extra density not explained by the atomic model involves a few disordered C-terminal residues of the capsid protein that were not part of the atomic model. It can be seen (Fig. 3c) that, as expected, the S. solfataricus filament has a significantly greater amount of peripheral density due to glycosylation than the P. arsenaticum filament. A prediction of the lesser glycosylation for the P. arsenaticum pilus is that it will not display the remarkable stability of the S. islandicus pilus in vitro26. Consistent with this prediction, boiling the S. islandicus pili in 5 M GuHCl failed to disassemble the filaments26, but under the same conditions the P. arsenaticum pili come apart (Supplementary Fig. 5). Collectively, these results suggest that SSRV1 and PFV2 recognize their corresponding receptors through different interactions. Whereas binding of SSRV1 to S. solfataricus pili is likely to be mediated through carbohydrate moieties, direct interaction with the pilin subunits might play an important role in the case of PFV2.

Evolutionary relationships

Expanding the number of archaeal T4P atomic structures from one to three allows for more reliable comparisons to now be made between these structures and both bacterial T4P and archaeal flagellar filaments. The most striking difference is that in both bacterial T4P and archaeal flagellins, the N-terminal α-helix is ~50 residues long, while in the archaeal T4P it is only ~35 residues long (Fig. 4a). By this criterion, the Iho670 adhesion filaments, previously described as “flagellar-like”25, appear to be a form of archaeal T4P. Despite the differences in the N-terminal helix length between archaeal flagellins and T4P, the helical symmetries of the filaments are quite similar (Fig. 4b). In contrast, although bacterial T4P can have a similar twist to the archaeal filaments (~ 100°), they have a distinctly different axial rise of ~10 Å as opposed to the ~5 Å in the archaeal filaments. In addition, all known bacterial T4P show a partial melting of the N-terminal helix, not seen in any of the archaeal filaments31.

Fig. 4: Conservation and divergence of the N-terminal helical bundles.
figure 4

a Sequence alignments of the N-terminal long helix in three archaeal flagellins, one archaeal “adhesion” protein, three archaeal T4P and three bacterial T4P. Area where the bacterial T4P N-terminal helix melts is indicated by two red arrows. b Helical symmetries of the filaments mentioned in a, with archaeal filaments light blue and bacterial filaments orange. c Five adjacent N-terminal helices of P. arsenaticum pilins, S. solfataricus pilins, I. hospitalis proteins, M. hungatei flagellins and N. gonorrhoeae pilins are shown. The Cα trace is shown in cartoon (left), with one helix colored cyan and the other four colored yellow. The bundles are also shown in an atomic surface view and colored by lipophilicity (right). d All-against-all comparison of the five helix bundles of the structures shown in a. The matrix is based on the pairwise RMSD comparisons calculated from PyMOL.

The distribution of helical symmetries among the archaeal filaments and bacterial T4P also suggests a conservation of how their long N-terminal α-helical tails pack together (Fig. 4b). Therefore, five adjacent copies of those α-helical tails were cut out from the filament model and compared with each other (Fig. 4c, d). Interestingly, Iho670 adhesion filament packs very similarly to S. solfataricus and S. islandicus pili, with an RMSD < 2 Å, while P. arsenaticum packs slightly differently from those three filaments with RMSDs of 3–4 Å (Fig. 4d). Notably, the crucial N-terminal subunit-subunit interactions in these four filaments are almost all hydrophobic (Fig. 4a, c), except for in P. arsenaticum there is a glutamic acid, which may contribute to the slightly different packing compared to Iho670 and other archaeal T4P. The archaeal flagellar filaments, judging by the sequence alignment and the RMSD matrix (Fig. 4a, d), have a very similar packing with Iho670 and the other archaeal T4Ps in their first 35 amino acids. However, their helices extend further with more hydrophilic residues interacting both with each other and with the globular domains, presumably providing greater mechanical stability in their roles as rotating propellers. Bacterial T4Ps, in contrast, have more hydrophilic residues in their N-terminal helices, including the conserved glutamic acid-forming key hydrogen bonds with N-terminal residues. Because of the melted N-terminal region seen thus far in every bacterial T4P, they have a completely different packing compared to archaeal filaments (Fig. 4c, d).

A DALI32 matrix analysis of the C-terminal globular domains (Fig. 5a) shows that archaeal flagellins, T4P and the Iho670 adhesion filament share structural homology for this domain containing an Ig-like β-sandwich. However, this domain in archaea shows no structural similarity to the bacterial T4P, where this globular domain is mainly a β-sheet containing 3-5 β-strands, or almost entirely absent in at least one pilin33. A similar matrix was seen when the C-terminal globular domains were analyzed by TM-score34 (Supplementary Fig. 6). TM-score is a metric for measuring the similarity of protein structures, and has a value in the range (0,1). It is a better metric in this instance, because it is independent of protein length, unlike RMSD analysis. Therefore, archaeal T4P and flagellins cannot be readily distinguished by the fold of the C-terminal domain, but can be easily distinguished simply by the length of the N-terminal helix.

Fig. 5: Conservation and divergence of the C-terminal globular domains.
figure 5

a All-against-all comparison of the bacterial T4P and other archaeal structures with N-terminal T4P domains. The N-terminal helices have been removed and only the globular domains were analyzed. The matrix is based on the pairwise Z-score comparisons calculated using the DALI server32. The color scale indicates the corresponding Z-scores. Based on their functions and origins, the proteins are partitioned into four groups, which are indicated with different colors on the right. One representative globular domain within each archaeal group was highlighted by a red dashed circle, to show the corresponding homology region. b Ribbon diagrams of the globular domains used in a.


Recent advances in cryo-EM have revolutionized the life sciences35,36,37. Besides yielding near-atomic resolution structures of complex macromolecular assemblies, this technique becomes increasingly valuable for de novo identification and characterization of protein components constituting these assemblies, whereby atomic models are built directly into the map densities. This approach has been particularly revealing in the study of complex virions38,39,40,41 and cellular appendages26. Here we have used cryo-EM to identify the host receptors recognized by two hyperthermophilic archaeal viruses, SSRV1 and PFV2. Studies on virus-host interactions remain highly challenging in archaea, due to the lack of genetic tools for most organisms, as is the case for the hosts of SSRV1 and PFV2. We have observed that both viruses bind to pili-like filaments and could determine the identity of the respective receptors directly by cryo-EM. We do not know how this would be possible using other approaches. For instance, mass-spectrometry analysis of a crude sample typically yields too many potential candidate proteins for unequivocal identification, whereas some proteins are not amenable to standard tryptic digestion, as has been shown recently for the pili of S. islandicus26.

Pili appear to be a common receptor for hyperthermophilic archaeal viruses and have been previously shown to be recognized by rudiviruses SIRV2 and SIRV816,17, and turrivirus STIV18. Here we have shown that members of yet another family of archaeal viruses, the Tristromaviridae, also bind to the host cells via T4P. Rudiviruses recognize the adhesive T4P26, whereas the identity of the pilus receptor of STIV on the surface of S. solfataricus has not been determined18. We do not exclude the possibility that the S. solfataricus T4P identified herein as the receptor for SSRV1 is an ortholog of the pilus recognized by STIV. Notably, direct adsorption experiments with SSRV1 to different members of the genera Sulfolobus and Saccharolobus showed that the virus could adsorb only to S. solfataricus POZ149 and, less efficiently, to S. solfataricus P1, but not to S. islandicus LAL14/1 or S. acidocaldarius DSM 63927, suggesting that efficient binding is highly specific. Intriguingly, in addition to the divergence of the pilin proteins themselves, there might be species-specific differences in the pilin glycosylation patterns, which could play equally important role in determining the host range of archaeal viruses. Thus, structural characterization of the glycans decorating different archaeal surface structures is likely to shed additional light on virus-host interactions in archaea.

The reasons underlying the selection of T4P as common virus receptors remain unclear. One possible explanation is that T4P are important for survival and functioning of hyperthermophilic archaea in natural habitats and hence the loss of these structures would bear a considerable fitness cost. Consistently, T4P are highly widespread in archaea and generally well conserved in members of the same genus13. Notably, it has been shown that besides its host S. solfataricus POZ149, SSRV1 can deliver its genome, with low efficiency, into a broad range of cells from genera Saccharolobus/Sulfolobus and Acidianus, even though genome delivery did not lead to virus proliferation27. An alternative explanation could be that the inherent properties of T4P might assist, directly or otherwise, in the genome delivery into the cell interior. For instance, T4P might be landmarks for the openings in the S-layer, an external crystalline protein layer surrounding archaeal cells42,43, which has to be penetrated during the delivery of the viral genome. Furthermore, it has been previously suggested that SIRV2 initially binds to the tips of T4P and progressively moves along the pilus to the cell body, where genome deliver takes place16. However, the mechanisms which would promote the virus movement and genome internalization remain to be understood. Additionally, if archaeal T4P retract, as they do in bacteria1, they would be ideal candidates as receptors for viruses as they could readily lead to the internalization of the viral genome. However, no PilT-like retraction ATPases have been found in archaea, and no direct observations of T4P retraction in archaea have been made thus far13. But the Tad pili in Caulobacter, which also lack a PilT-like retraction ATPase, have now been shown to retract44. We therefore leave this possibility of pilus retraction open.

Being exposed on the cell surface, T4P of hyperthermophilic archaea represent an excellent model for studying the remarkable stability of macromolecular complexes under extreme physico-chemical conditions. Previous study of the S. islandicus T4P has revealed that extreme hydrophobicity coupled with extensive glycosylation renders the pilus resistant to various harsh treatments, including boiling in SDS and GuHCl or prolonged treatment with proteases26. Comparison of T4P from different hyperthermophiles allows us to dissect further the factors underlying adaptations to different environmental conditions. First, although T4P of a neutrophilic P. arsenaticum is as hydrophobic as those of acidophilic S. islandicus and S. solfataricus (Fig. 2c), it does not possess the extensive sugar coating. This observation suggests that glycosylation plays a more important role for survival in acidic environments. Recently, another adaptation to low pH habitats has been uncovered in archaea-specific glycerol dibiphytanyl glycerol tetraethers (GDGTs) lipids. Headgroups of GDGT in acidophilic hyperthermophiles are covalently linked to calditol, a unique five-membered ring, which is synthesized from a hexose sugar moiety45. Decoration of pili and lipids with covalently linked glycans and calditol, respectively, appear to be conceptually similar adaptations to acidic environments. Instead, T4P of P. arsenaticum is stabilized by an intramolecular disulfide bond (Fig. 2f), a protein adaptation to high temperatures previously reported in bacteria, archaea and their viruses46,47,48. Disulfides in mesophilic bacterial T4P have also been previously described49. Notably, qualitative observations suggest that P. arsenaticum T4P do not possess the remarkable resilience observed for Sulfolobus T4P (Supplementary Fig. 5), suggesting that it may be glycosylation rather than hydrophobicity which renders the pilus nearly indestructible.

While it was previously suggested that the Iho670 adhesion filaments from the non-motile archaeon I. hospitalis were “flagellar-like”25, we have now shown that all archaeal T4P (or at least, the three structures that now exist) are truly flagellar-like in comparison with the atomic structures for archaeal flagellar filaments. Further, the Ih0670 filaments are much closer to archaeal T4P than to flagellar filaments, particularly in terms of the N-terminal helix that fails to extend into the C-terminal globular domain. Thus, we think it likely that there may be many other archaeal proteins that are not identified at this point as T4P. Given that the C-terminal domains of T4P-like filaments in bacteria and archaea are unrelated and some bacteria lack this domain altogether33, it appears likely that the N-terminal domain consisting of the signal sequence and the hydrophobic α-helix, which forms the core of the filament, has evolved first, possibly at the stage of the last universal cellular ancestor (LUCA). In contrast, the C-terminal globular domains have emerged later on, independently in Bacteria and Archaea. Consistent with this, a novel T4P fold has now been found in bacteria, where the C-terminal domain is all α-helical50. The archaeal C-terminal domain is clearly related to immunoglobulin-like domains which are widespread in all walks of life51. Thus, the contemporary archaeal T4P-like filaments are a result of a fusion of two pre-existing structural domains, a common mechanism of protein evolution and diversification52,53. Importantly, a close structural similarity between archaeal pili and flagellar filaments (Fig. 5) strongly suggests that functional diversification of the two types of archaeal filaments took place following the split of bacterial and archaeal lineages from their common ancestor.


Strain cultivation and filament purification

Exponentially growing cultures of Saccharolobus solfataricus POZ14927 and Pyrobaculum arsenaticum 2GA54 cells were infected with fresh preparations of Saccharolobus solfataricus rod-shaped virus 1 (SSRV1) and Pyrobaculum filamentous virus 2 (PFV2), respectively. The infected culture of S. solfataricus POZ149 was incubated at 75 °C under agitation for 2 days, whereas P. arsenaticum 2GA culture was grown during 4 days at 90 °C without shaking. After the removal of cells (7438 × g, 20 min, Sorvall 1500 rotor), viruses along with pili detached from the cells were collected and concentrated by ultracentrifugation (273,620 × g, 2 h, 10 °C, Beckman 126 SW41 rotor). For cryo-EM analysis, the concentrated particles were resuspended in buffer A55: 20 mM KH2PO4, 250 mM NaCl, 2.14 mM MgCl2, 0.43 mM Ca(NO3)2 and <0.001% trace elements of Sulfolobales medium, pH 6. Virus particles and pili also copurified when the pelleted virion-pili mixtures were subjected to centrifugation in a CsCl buoyant density gradient (0.45 g ml−1) with a Beckman SW41 rotor at 260,110 x g for 20 h at 10 °C.

DNA extraction, sequencing and genome analysis

DNA was extracted from exponentially growing cultures of S. solfataricus POZ149 and P. arsenaticum 2GA using the Wizard Genomic DNA Purification Kit (Promega). The genome sequence of S. solfataricus POZ149 was obtained using PacBio single-molecule real-time (SMRT) technology, while libraries with 250 bp insert size were sequenced on Illumina platform for P. arsenaticum 2GA (Novogen, China). Raw sequence reads were processed and assembled with FALCON56 and SOAPdenovo version 2.0457, respectively. Gene prediction was performed by GeneMark.hmm version 3.2558. The genome sequence of S. solfataricus POZ149 was deposited in GenBank under the accession number CP050869. The Whole Genome Shotgun project for P. arsenaticum 2GA has been deposited at DDBJ/ENA/GenBank under the accession JAAVJF000000000. The version described in this paper is version JAAVJF010000000.

Negative-stain electron microscopy

For TEM, 5 µl of the samples were applied to carbon‐coated copper grids and negatively stained with 2% uranyl acetate. The stained grids were imaged with the transmission electron microscope FEI Tecnai Biotwin (Institut Pasteur, France).

Cryo-electron microscopy and image analysis

The pilus sample (~4.0 μl) was applied to discharged lacey carbon grids and plunge frozen using a Vitrobot Mark IV (FEI). Frozen grids were imaged in a Titan Krios at 300 keV and recorded with a K3 camera at 1.08 Å/pixel. The P. arsenaticum pilus data were collected in the UVA core facility, and the S. solfataricus pilus was collected in National Cryo-EM Facility (NCEF) of the National Cancer Institute (NCI). Micrographs were collected using a defocus range of 1–2 μm, with a total exposure dose of ~50 electrons/Å2 distributed into ~25 fractions. To get a preliminary helical reconstruction volume in SPIDER59, all of the micrographs were first motion corrected and dose weighted by MotionCorr v2, and then CTF-multiplicated by the theoretical CTF. Filament images amounting to ~20 electrons /Å2 were extracted by EMAN260. A small subset containing ~50,000 overlapping 384-pixel-long segments was used to search for the correct helical symmetry. For P. arsenaticum we explored a multiplicity of symmetries that were each consistent with the averaged power spectrum. The number of possible symmetries was six (Supplementary Table 2), and each of these was tested in SPIDER59 using IHRSR61, until recognizable protein features were seen, such as side-chains. A ~4 Å reconstruction was generated from this small subset with the correct symmetry (entry #1, Supplementary Table 2), and this volume was subsequently filtered to 7 Å as the starting reference used in RELION62. For S. solfataricus, the high degree of sequence identity with the S. islandicus LAL14/1 pilus suggested that a helical symmetry close to that previously determined26 for S. islandicus might be the correct one, and this turned out to be the case. After using the full dataset in RELION (210,331 segments for the P. arsenaticum pilus, 579,713 segments for the S. solfataricus pilus, Table 1), doing CTF-refinement and Bayesian polishing, the final volumes were estimated to have a resolution of 3.8 Å for the P. arsenaticum pilus and 3.4 Å for the S. solfataricus pilus, based on the map:map FSC, model:map FSC and d9930. The final volumes were then sharpened with a negative B-factor automatically estimated in RELION (Table 1).

Model building

The density corresponding to a single S. solfataricus pilin was segmented from the experimental cryo-EM density map using Chimera63. Then a S. solfataricus pilin model was generated by homology modeling using the S. islandicus LAL14/1 pilin as the reference, and then docked into the segmented map. Then this model was adjusted manually in Coot and real-space refined in PHENIX64. Finally, the refined single pilin model was used to generate a filamentous model using the determined helical symmetry, and this filament model was refined against the full cryo-EM map using in PHENIX. MolProbity65 was used to evaluate the quality of the filament model. The refinement statistics are shown in Table 1.

The density corresponding to a single P. arsenaticum pilin was also segmented in the same manner. Due to the uncertainty in the pilin sequence, seven potential pilin candidates were selected based on secondary structure predictions (WP_011899639, WP_011900226, WP_011899654, WP_011900935, WP_011900944, WP_011900938, and WP_011900942). Each of the sequences was used to do de novo model building against the segmented map using Rosetta CM66. As a result, only HC235_07175 could be built into the cryo-EM map and was also detected by MS/MS analysis. To further validate the sequence of both pilin, the whole genomes of both strains were sequenced and deposited. The model building for the assembled P. arsenaticum pilus was the same as described above.

Mass spectrometry

The solution samples containing the pili were reduced with 10 mM DTT in 0.1 M ammonium bicarbonate then alkylated with 50 mM iodoacetamide in 0.1 M ammonium bicarbonate (both room temperature for 0.5 h). The sample was then digested overnight at 37 °C with 0.1 µg (Chymotrypsin, Asp-N and Trypsin) in 50 mM ammonium bicarbonate. The sample was acidified with acetic acid to stop digestion and then spun down. The solution was evaporated to 15 µL for MS analysis.

The LC-MS system consisted of a Thermo Electron Q Exactive HF-X mass spectrometer system with an Easy Spray ion source connected to a Thermo 75 µm x 15 cm C18 Easy Spray column. 7 µL of the extract was injected and the peptides eluted from the column by an acetonitrile/0.1 M formic acid gradient at a flow rate of 0.3 µL/min over 1.0 hours. The nanospray ion source was operated at 1.9 kV. The digest was analyzed using the rapid switching capability of the instrument acquiring a full scan mass spectrum to determine peptide molecular weights followed by product ion spectra (10 HCD) to determine amino acid sequence in sequential scans. This mode of analysis produces approximately 25,000 MS/MS spectra of ions ranging in abundance over several orders of magnitude. Not all MS/MS spectra are derived from peptides. The data were analyzed by database searching using the Sequest search algorithm against Uniprot Sulfolobus solfataricus or Uniprot Pyrobaculum arsenaticum.

Data availability

The genome sequence of S. solfataricus POZ149 was deposited in GenBank under the accession number CP050869. The Whole Genome Shotgun project for P. arsenaticum 2GA has been deposited at DDBJ/ENA/GenBank under the accession number JAAVJF000000000. The version described in this paper is JAAVJF010000000. The atomic model for the P. arsenaticum pilus was deposited at the Protein Data Bank with accession code 6W8U, and the corresponding map was deposited at the Electron Microscopy Data Bank with code EMD-21578. The atomic model for the S. solfataricus pilus was deposited at the Protein Data Bank with accession code 6W8X, and the corresponding map was deposited at the Electron Microscopy Data Bank with code EMD-21579. Other data are available from the corresponding authors upon reasonable request.


  1. Craig, L., Forest, K. T. & Maier, B. Type IV pili: dynamics, biophysics and functional consequences. Nat. Rev. Microbiol. 17, 429–440 (2019).

    CAS  PubMed  Google Scholar 

  2. Giltner, C. L., Nguyen, Y. & Burrows, L. L. Type IV pilin proteins: versatile molecular modules. Microbiol. Mol. Biol. Rev.: MMBR 76, 740–772 (2012).

    CAS  PubMed  PubMed Central  Google Scholar 

  3. Lu, S. et al. Nanoscale pulling of type IV pili reveals their flexibility and adhesion to surfaces over extended lengths of the pili. Biophys. J. 108, 2865–2875 (2015).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  4. Craig, L., Pique, M. E. & Tainer, J. A. Type IV pilus structure and bacterial pathogenicity. Nat. Rev. Microbiol. 2, 363–378 (2004).

    CAS  PubMed  Google Scholar 

  5. Daum, B. & Gold, V. Twitch or swim: towards the understanding of prokaryotic motion based on the type IV pilus blueprint. Biol. Chem. 399, 799–808 (2018).

    CAS  PubMed  Google Scholar 

  6. Chang, C. Y. Surface sensing for biofilm formation in Pseudomonas aeruginosa. Front Microbiol. 8, 2671 (2017).

    PubMed  Google Scholar 

  7. Piepenbrink, K. H. DNA uptake by type IV filaments. Front Mol. Biosci. 6, 1 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  8. Bayley, D. P. & Jarrell, K. F. Further evidence to suggest that archaeal flagella are related to bacterial type IV pili. J. Mol. Evol. 46, 370–373 (1998).

    CAS  PubMed  Google Scholar 

  9. Faguy, D. M., Jarrell, K. F., Kuzio, J. & Kalmokoff, M. L. Molecular analysis of archael flagellins: similarity to the type IV pilin-transport superfamily widespread in bacteria. Can. J. Microbiol. 40, 67–71 (1994).

    CAS  PubMed  Google Scholar 

  10. Albers, S. V. & Pohlschroder, M. Diversity of archaeal type IV pilin-like structures. Extremophiles 13, 403–410 (2009).

    CAS  PubMed  Google Scholar 

  11. Albers, S. V., Szabo, Z. & Driessen, A. J. Archaeal homolog of bacterial type IV prepilin signal peptidases with broad substrate specificity. J. Bacteriol. 185, 3918–3925 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  12. Albers, S. V. & Jarrell, K. F. The archaellum: an update on the unique archaeal motility structure. Trends Microbiol. 26, 351–362 (2018).

    CAS  PubMed  Google Scholar 

  13. Makarova, K. S., Koonin, E. V. & Albers, S. V. Diversity and evolution of type IV pili systems in archaea. Front Microbiol. 7, 667 (2016).

    PubMed  PubMed Central  Google Scholar 

  14. Pohlschroder, M. & Esquivel, R. N. Archaeal type IV pili and their involvement in biofilm formation. Front Microbiol. 6, 190 (2015).

    PubMed  PubMed Central  Google Scholar 

  15. Chaudhury, P., Quax, T. E. F. & Albers, S. V. Versatile cell surface structures of archaea. Mol. Microbiol. 107, 298–311 (2018).

    CAS  PubMed  Google Scholar 

  16. Quemin, E. R. et al. First insights into the entry process of hyperthermophilic archaeal viruses. J. Virol. 87, 13379–13385 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  17. Rowland, E. F., Bautista, M. A., Zhang, C. & Whitaker, R. J. Surface resistance to SSVs and SIRVs in pilin deletions of Sulfolobus islandicus. Mol. Microbiol. (2019).

    Article  PubMed  PubMed Central  Google Scholar 

  18. Hartman, R. et al. The molecular mechanism of cellular attachment for an archaeal virus. Structure 27, 1634–1646 (2019).

    CAS  PubMed  Google Scholar 

  19. Wang, F. et al. Cryoelectron microscopy reconstructions of the Pseudomonas aeruginosa and Neisseria gonorrhoeae type IV pili at sub-nanometer resolution. Structure 25, 1423–1435 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  20. Kolappan, S. et al. Structure of the Neisseria meningitidis Type IV pilus. Nat. Commun. 7, 13015 (2016).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  21. Neuhaus, A. et al. Cryo-electron microscopy reveals two distinct type IV pili assembled by the same bacterium. Nat. Commun. 11, 2231 (2020).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  22. Poweleit, N. et al. CryoEM structure of the Methanospirillum hungatei archaellum reveals structural features distinct from the bacterial flagellum and type IV pili. Nat. Microbiol. 2, 16222 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  23. Daum, B. et al. Structure and in situ organisation of the Pyrococcus furiosus archaellum machinery. eLife 6, e27470 (2017).

  24. Meshcheryakov, V. A. et al. High-resolution archaellum structure reveals a conserved metal-binding site. EMBO reports 20, (2019).

  25. Braun, T. et al. Archaeal flagellin combines a bacterial type IV pilin domain with an Ig-like domain. Proc. Natl Acad. Sci. USA 113, 10352–10357 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  26. Wang, F. et al. An extensively glycosylated archaeal pilus survives extreme conditions. Nat. Microbiol. 4, 1401–1410 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  27. Baquero, D. P. C. P. et al. New virus isolates from Italian hydrothermal environments underscore the biogeographic pattern in archaeal virus communities. ISME J. 141821–1833 (2020).

    Article  PubMed  PubMed Central  Google Scholar 

  28. Wang, F. B. et al. M. Structure of a filamentous virus uncovers familial ties within the archaeal virosphere. Virus Evolution (2020).

  29. Egelman, E. H. Ambiguities in helical reconstruction. eLife 3, e04969 (2014).

    PubMed Central  Google Scholar 

  30. Afonine, P. V. et al. New tools for the analysis and validation of cryo-EM maps and atomic models. Acta Crystallogr D. Struct. Biol. 74, 814–840 (2018).

    CAS  PubMed  PubMed Central  Google Scholar 

  31. Egelman, E. H. Cryo-EM of bacterial pili and archaeal flagellar filaments. Curr. Opin. Struct. Biol. 46, 31–37 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  32. Holm, L. & Rosenstrom, P. Dali server: conservation mapping in 3D. Nucleic Acids Res 38, W545–W549 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  33. Reardon, P. N. & Mueller, K. T. Structure of the type IVa major pilin from the electrically conductive bacterial nanowires of Geobacter sulfurreducens. J. Biol. Chem. 288, 29260–29266 (2013).

    CAS  PubMed  PubMed Central  Google Scholar 

  34. Xu, J. & Zhang, Y. How significant is a protein structure similarity with TM-score = 0.5? Bioinformatics 26, 889–895 (2010).

    CAS  PubMed  PubMed Central  Google Scholar 

  35. Kuhlbrandt, W. Biochemistry The resolution revolution. Science 343, 1443–1444 (2014).

    ADS  PubMed  Google Scholar 

  36. Egelman, E. H. The current revolution in Cryo-EM. Biophys. J. 110, 1008–1012 (2016).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  37. Bai, X. C., McMullan, G. & Scheres, S. H. How cryo-EM is revolutionizing structural biology. Trends Biochem. Sci. 40, 49–57 (2015).

    CAS  PubMed  Google Scholar 

  38. Yuan, S. et al. Cryo-EM structure of a herpesvirus capsid at 3.1 A. Science 360, (2018).

  39. Fang, Q. et al. Near-atomic structure of a giant virus. Nat. Commun. 10, 388 (2019).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  40. Wang, F. et al. A packing for A-form DNA in an icosahedral virus. Proc. Natl Acad. Sci. USA 116, 22591–22597 (2019).

    CAS  PubMed  PubMed Central  Google Scholar 

  41. Veesler, D. et al. Atomic structure of the 75 MDa extremophile Sulfolobus turreted icosahedral virus determined by CryoEM and X-ray crystallography. Proc. Natl Acad. Sci. USA 110, 5504–5509 (2013).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  42. Kandiba, L. & Eichler, J. Archaeal S-layer glycoproteins: post-translational modification in the face of extremes. Front Microbiol. 5, 661 (2014).

    PubMed  PubMed Central  Google Scholar 

  43. Klingl, A. & Pickl, C., . & Flechsler, J. Archaeal cell walls. Subcell. Biochem. 92, 471–493 (2019).

    CAS  PubMed  Google Scholar 

  44. Ellison, C. K. et al. Obstruction of pilus retraction stimulates bacterial surface sensing. Science 358, 535–538 (2017).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  45. Zeng, Z., Liu, X. L., Wei, J. H., Summons, R. E. & Welander, P. V. Calditol-linked membrane lipids are required for acid tolerance in Sulfolobus acidocaldarius. Proc. Natl Acad. Sci. USA 115, 12932–12937 (2018).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  46. Beeby, M. et al. The genomics of disulfide bonding and protein stabilization in thermophiles. PLoS Biol. 3, e309 (2005).

    PubMed  PubMed Central  Google Scholar 

  47. Krupovic, M., White, M. F., Forterre, P. & Prangishvili, D. Postcards from the edge: structural genomics of archaeal viruses. Adv. virus Res. 82, 33–62 (2012).

    CAS  PubMed  Google Scholar 

  48. Menon, S. K. et al. Cysteine usage in Sulfolobus spindle-shaped virus 1 and extension to hyperthermophilic viruses in general. Virology 376, 270–278 (2008).

    CAS  Article  PubMed  Google Scholar 

  49. Hartung, S. et al. Ultrahigh resolution and full-length pilin structures with insights for filament assembly, pathogenic functions, and vaccine potential. J. Biol. Chem. 286, 44254–44265 (2011).

    CAS  PubMed  PubMed Central  Google Scholar 

  50. Sheppard, D. et al. The major subunit of widespread competence (pseudo)pili exhibits a novel and conserved type IV pilin fold. Preprint at (2020).

  51. Bork, P., Holm, L. & Sander, C. The immunoglobulin fold. Structural classification, sequence patterns and common core. J. Mol. Biol. 242, 309–320 (1994).

    CAS  PubMed  Google Scholar 

  52. Dohmen, E., Klasberg, S., Bornberg-Bauer, E., Perrey, S. & Kemena, C. The modular nature of protein evolution: domain rearrangement rates across eukaryotic life. BMC Evol. Biol. 20, 30 (2020).

    CAS  PubMed  PubMed Central  Google Scholar 

  53. Moore, A. D., Bjorklund, A. K., Ekman, D., Bornberg-Bauer, E. & Elofsson, A. Arrangements in the modular evolution of proteins. Trends Biochem. Sci. 33, 444–451 (2008).

    CAS  PubMed  Google Scholar 

  54. Rensen, E. I. et al. A virus of hyperthermophilic archaea with a unique architecture among DNA viruses. Proc. Natl Acad. Sci. USA 113, 2478–2483 (2016).

    ADS  CAS  PubMed  PubMed Central  Google Scholar 

  55. Quemin, E. R. et al. Sulfolobus spindle-shaped virus 1 contains glycosylated capsid proteins, a cellular chromatin protein, and host-derived lipids. J. Virol. 89, 11681–11691 (2015).

    CAS  PubMed  PubMed Central  Google Scholar 

  56. Chin, C. S. et al. Phased diploid genome assembly with single-molecule real-time sequencing. Nat. Methods 13, 1050–1054 (2016).

    CAS  PubMed  PubMed Central  Google Scholar 

  57. Li, R., Li, Y., Kristiansen, K. & Wang, J. SOAP: short oligonucleotide alignment program. Bioinformatics 24, 713–714 (2008).

    CAS  PubMed  Google Scholar 

  58. Besemer, J., Lomsadze, A. & Borodovsky, M. GeneMarkS: a self-training method for prediction of gene starts in microbial genomes. Implications for finding sequence motifs in regulatory regions. Nucleic Acids Res. 29, 2607–2618 (2001).

    CAS  PubMed  PubMed Central  Google Scholar 

  59. Frank, J. et al. SPIDER and WEB: processing and visualization of images in 3D electron microscopy and related fields. J. Struct. Biol. 116, 190–199 (1996).

    CAS  PubMed  Google Scholar 

  60. Tang, G. et al. EMAN2: an extensible image processing suite for electron microscopy. J. Struct. Biol. 157, 38–46 (2007).

    CAS  PubMed  Google Scholar 

  61. Egelman, E. H. A robust algorithm for the reconstruction of helical filaments using single-particle methods. Ultramicroscopy 85, 225–234 (2000).

    CAS  PubMed  Google Scholar 

  62. He, S. & Scheres, S. H. W. Helical reconstruction in RELION. J. Struct. Biol. 198, 163–176 (2017).

    CAS  PubMed  PubMed Central  Google Scholar 

  63. Pettersen, E. F. et al. UCSF Chimera-a visualization system for exploratory research and analysis. J. Comput. Chem. 25, 1605–1612 (2004).

    CAS  PubMed  Google Scholar 

  64. Adams, P. D. et al. PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. Sect. D., Biol. Crystallogr. 66, 213–221 (2010).

    CAS  Google Scholar 

  65. Williams, C. J. et al. MolProbity: more and better reference data for improved all-atom structure validation. Protein Sci. 27, 293–315 (2018).

    CAS  PubMed  Google Scholar 

  66. Song, Y. et al. High-resolution comparative modeling with RosettaCM. Structure 21, 1735–1742 (2013).

    CAS  PubMed  Google Scholar 

  67. Poirot, O., O’Toole, E. & Notredame, C. Tcoffee@igs: a web server for computing, evaluating and combining multiple sequence alignments. Nucleic Acids Res. 31, 3503–3506 (2003).

    CAS  PubMed  PubMed Central  Google Scholar 

  68. Clamp, M., Cuff, J., Searle, S. M. & Barton, G. J. The Jalview Java alignment editor. Bioinformatics 20, 426–427 (2004).

    CAS  PubMed  Google Scholar 

Download references


This research was, in part, aided by the National Cancer Institute’s National Cryo-EM Facility at the Frederick National Laboratory for Cancer Research under contract HSSN261200800001E. Cryo-EM imaging was also conducted at the Molecular Electron Microscopy Core facility at the University of Virginia, which is supported by the School of Medicine and built with NIH grant G20-RR31199. This work was supported by NIH grant R35GM122510 (to E.H.E.). M.K. was supported by l’Agence Nationale de la Recherche (France) project ENVIRA. D.P.B. is part of the Pasteur – Paris University (PPU) International PhD Program, which has received funding from the European Union’s Horizon 2020 research and innovation programme under the Marie Sklodowska-Curie grant agreement No 665807. We are also grateful to the Ultrastructural BioImaging (UTechS UBI) unit of Institut Pasteur for access to electron microscopes.

Author information

Authors and Affiliations



D.P.B. prepared all of the samples; F.W. collected the cryo-EM data; F.W., L.B. and E.H.E. performed image processing; F.W. did the structural modeling; F.W., Z.S. and M.K. prepared figures; F.W., M.K. and E.H.E. wrote the manuscript; E.H.E., D.P. and M.K. conceived the study.

Corresponding authors

Correspondence to Mart Krupovic or Edward H. Egelman.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Peer review information Nature Communications thanks Han Remaut, Matthias Wolf and the other, anonymous, reviewer(s) for their contribution to the peer review of this work. Peer reviewer reports are available.

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Wang, F., Baquero, D.P., Su, Z. et al. The structures of two archaeal type IV pili illuminate evolutionary relationships. Nat Commun 11, 3424 (2020).

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI:

Further reading


By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.


Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing