In light of the recent accumulated knowledge on SARS-CoV-2 and its mode of human cells invasion, the binding of viral spike glycoprotein to human Angiotensin Converting Enzyme 2 (hACE2) receptor plays a central role in cell entry. We designed a series of peptides mimicking the N-terminal helix of hACE2 protein which contains most of the contacting residues at the binding site, exhibiting a high helical folding propensity in aqueous solution. Our best peptide-mimics are able to block SARS-CoV-2 human pulmonary cell infection with an inhibitory concentration (IC50) in the nanomolar range upon binding to the virus spike protein with high affinity. These first-in-class blocking peptide mimics represent powerful tools that might be used in prophylactic and therapeutic approaches to fight the coronavirus disease 2019 (COVID-19).
The coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome-coronavirus 2 (SARS-CoV-2) has emerged as a pandemic, claiming at the time of writing more than 1.3 million deaths and over 57 millions confirmed cases world-wide between December 2019 and November 20201. Since the SARS-CoV-2 discovery2,3 and identification, the energy deployed by the scientific community has made it possible to generate an extraordinary wealth of information. However, to date, efficient therapeutics or drugs are lacking and prevention of the disease relies only on non-specific barrier measures4. Indeed, no specific drugs targeting the virus are available5 yet, many clinical trials have been engaged with SARS-CoV-2 non-specific treatments4. The structural and biochemical basis of the mechanism of infection has been investigated, highlighting that the virus cell-surface spike protein of SARS-CoV-2 targets human receptors6,7. Human angiotensin converting enzyme 2 (hACE2) and the cellular transmembrane protease serine 2 (TMPRSS2) have been identified as major actors of the virus entry into human cells8.
With the goal of preventing the SARS-CoV-2 from infecting human cells, blocking the interaction between hACE2 and the virus spike protein has been validated. Indeed, inhibition of SARS-CoV-2 infections in engineered human tissues using clinical-grade soluble ACE2 was recently demonstrated9. Likewise, an engineered stable mini-protein mimicking three helices of hACE2 to plug SARS-CoV-2 spikes10 was described, but its capacity to block viral infection was not demonstrated. Although several in silico designed peptides were proposed to prevent formation of the fusion core11,12, first attempts to design a peptide binder derived from hACE2 proved to be a difficult task, leading to mitigated results13.
Thus, starting from the published crystal structure of SARS-CoV-2 spike receptor-binding domain (RBD) bound to hACE214, we designed peptide-mimics of the N-terminal hACE2 helix which interact with the spike protein. We report here the strategy implemented to optimize the design of our peptide mimics, their high helical folding propensity in water, their ability to block SARS-CoV-2 human pulmonary cell infection with an IC50 in the nanomolar range and their binding to spike RBD with strong affinity. We also demonstrated the non-toxicity of our mimics at concentrations 150 times higher than the IC50 on pulmonary cell lines.
Design of peptides mimicking the helix H1 of hACE2
We first examined the complex between hACE2 and the surface spike protein of SARS-CoV-2 (PDB 6m0j)14 in order to highlight the important contacts and some relevant characteristics of the interacting hACE2 sequence (Fig. 1).
Twenty residues from hACE2 were identified14 as to be in close contacts with the Spike protein, using a distance cut-off of 4 Å. These interactions occur mainly through the N-terminal α-helix H1 of hACE2 (Fig. 1a). This α-helix (Fig. 1b), composed of 27 residues (from S19 to L45, Fig. 1c) contains 12 residues (highlighted in magenta in Fig. 1c) involved in hydrogen bonds, salt bridges, and van der Waals interactions (see Supplementary Table 1 for details)14.
A Clustal multiple sequence alignment of viruses isolated in China, United States and France was performed (See Supplementary Fig. 1). From these analyses, we observed that all the randomly selected sequences were 100% identical at least in the ACE2 interacting interface. This highlights a highly conserved sequence for the portion of spike interacting with the α-helix H1 of hACE2, possibly because deleterious mutations at this interface would limit viral infectivity.
Our strategy was designing a peptide with a high helical folding propensity and retaining most of the binding affinity of hACE2 to the spike RBD of SARS-CoV-2, using natural amino acids15. Indeed, we preferred not to use complex chemical tools known to stabilize α-helix16,17 in order to limit developability constraints. Our mimics were designed and optimized for binding, high helical content and low antigenicity, to avoid triggering a neutralizing immune response that would compromise the peptide therapeutic potential. A combination of the Agadir program18,19, an algorithm developed to predict the helical content of peptides and the semi-empirical method reported by Kolaskar20 to highlight the number of antigenic determinants, was iteratively used.
We observed that the N-terminal sequence of the H1 helix, composed of four residues (S19TIE22), corresponds to a consensus N-capping box motif (SXXE)21. A capping box features reciprocal backbone-side-chain hydrogen-bonds favoring a helix initiation. Although this sequence does not adopt the H-bonded capping conformation in the crystal structure of the full protein, it could constitute a stabilizing element in the isolated helix when extracted from the protein context. These observations led us to keep 14 residues from the native H1 helix of hACE2 as contact residues or putative stabilizing capping box. The 13 remaining residues that are not essential for the interaction were considered as possible sites for amino acid substitutions (Fig. 1c). We thus substituted non-essential positions by Ala and/or Leu residues which display higher helical folding propensities, and we calculated the peptide helical content after each substitution (Supplementary Table 2).
A peptide sequence optimization was then carried out to lower the antigenicity while keeping the helical propensity thanks to an iterative residue scanning and calculation of the helical content variation upon new substitutions (Supplementary Table 3). This strategy highlighted the influence of the residue N33 in the native sequence. Indeed, if the N33/L33 substitution systematically improved the helical content, it was always at the expense of antigenicity. Conversely, the L33/N33 substitution reduced the antigenicity at the expense of helical content. The solution was found by L33/M33 substitution which decreased the number of AD.
The H1 helix of ACE2 adopts a kinked conformation in the crystal structure, leading to a distorted CO/HN hydrogen bond network between H34/D38 and E35/L39 residues. Therefore, we considered introducing a proline, as this residue is known to induce local kinks or distortions in natural helices22,23. D38 was classed as a contact residue, while L39 side chain is not involved in any direct interaction. Consequently, L39 position was selected for substitution by proline (peptide P5, Table 1).
In order to increase the helical content to a maximum level, this iterative study was also applied to longer peptide sequences starting from the 29-residue native one, albeit at the expense of antigenicity. Diverse combinations of N- and C-terminus capping groups were also considered (free extremities or N-acetyl, C-carboxamide groups).
Finally, we examined the possibility of promoting additional side chain contacts provided by ACE2 residues that do not belong to H1 helix. Y83 residue in H2 helix appeared as a good candidate as it lies very close in space to A25 in H1 helix (Fig. 1a). Molecular modeling was carried out on H1 helix analogs in which A25 was replaced by tyrosine or homotyrosine (hTyr) residues (Supplementary Fig. 2). Calculations showed that hTyr residue was able to project the phenol ring in an adequate orientation to mimic Y83 position. Of note, hTyr is a natural amino acid24.
Three peptides were selected as controls in our optimization process, P1 (native sequence), P1scr (scrambled peptide from P1), and Ppen (described by Pentelute and colleagues in a longer biotinylated and pegylated construct and termed SBP1 as a putative spike binder13).
The results highlighting the progression in helical content and number of antigenic determinants are reported in Table 1 for the most relevant peptide mimics (see Supplementary Tables 2–4 for all the peptide-mimics that were designed and/or synthesized). These peptides were synthesized on a 5-mg to 20-mg scale from Fmoc-protected amino acids utilizing standard solid-phase peptide synthesis methods on rink amide resin (see Methods section).
The designed peptides highlight an excellent correlation between calculated and experimentally determined helical content by circular dichroism in aqueous media
The conformation of synthesized peptides in aqueous solution was investigated by circular dichroism (CD) spectroscopy25. Figure 2 shows the superimposed CD spectra of 12 peptides, including control ones, i.e., P1 (native sequence), P1scr (Scramble), and Ppen. The CD spectra of peptides P1 (native), P1scr (scrambled) are characteristic of a predominant random coil structure with a negative minimum near 200 nm, as expected. Similarly, Ppen described as a helical peptide sequence13 also adopted a random coil conformation in solution. For all other peptides, the CD spectra exhibit a canonical α-helix signature, featuring a double minimum around 208 nm and 222 nm, with the exception of the proline-containing P5 peptide. The deconvolution of the CD spectra using DichroWeb25 allowed us to estimate the helical population for each peptide, which is reported in Table 1. Overall, an excellent agreement was observed between the Agadir-computed values and the experimental helical population inferred from CD data. The native hACE2 H1 helix sequence (peptides P1, Ppen) has a weak propensity to fold into an α-helix in aqueous solution (below 10%). In contrast, the sequence optimization led to H1 analogs exhibiting a high helical propensity (between 50 and 80%). The introduction of a proline residue in peptide P5 has a strong destabilizing effect on helical conformation (17%) whereas Leu/hTyr substitution only led to a slight decrease of the helical content (P7 versus P6 and P10 versus P8).
Peptide mimics of hACE2 show high anti-infective efficacy and are devoid of cell toxicity
To determine whether our peptide mimics of hACE2 H1 helix block SARS-CoV-2 cell infection, antiviral assays26 were performed (Fig. 3) with a SARS-CoV-2 clinical isolate obtained from bronchoalveolar lavage (BAL) of a symptomatic infected patient (#SARS-CoV-2/PSL2020) at Pitié-Salpêtrière hospital, Paris (France) (see Methods section). We first measured the inhibition of viral replication in Vero-E6 cell cultures exposed to 10 µM of the first set of peptide-mimics (P2 to P8, P1, P1scr, and Ppen being used as controls), for 48 h (Fig. 3a). These preliminary assays helped us to identify two peptide-mimics that stand out (P7 and P8) for their ability to block the viral infection, highlighting a potential role of hTyr. This observation helped us in the peptide-mimics structure optimization process. Two new peptides were designed, P9 and P10 incorporating the hTyr residue and evaluated with P8 for their ability to block viral infection on Vero-E6 cells through the measurement of infectious virus production and viral genome (Fig. 3b and Supplementary Fig. 3)27. These peptides proved to be devoid of toxicity in Vero-E6 (Fig. 3c). In order to get insight on their ability to block viral infection on human pulmonary cells, Calu-3 cell line (ATCC HTB55) was chosen. This pulmonary epithelial cell line is commonly used as a respiratory models in preclinical applications28 and SARS-CoV-2 has been shown to replicate efficiently in this cell line29.
We first observed a dose-dependent reduction in virus titer (Fig. 3d) and then, using ELISA assays we evaluated the average median inhibitory concentration (IC50) on Calu-3 cells for P8, P9, and P10 to be 46 nM, 53 nM, and 42 nM respectively (Fig. 3e). Importantly, no cytotoxicity was observed in similarly treated uninfected culture cells at 10 μM, a concentration 150 times higher than the IC50 (Fig. 3f). Collectively, these data demonstrate the high antiviral potency of peptide analogs P8, P9, and P10.
The designed peptides bind to SARS-CoV-2 spike RBD with high affinity
Finally, the peptides that were able to block cell infection with an IC50 in the sub-µM range (P8, P9, and P10) were evaluated for their ability to bind to SARS-CoV-2 spike RBD (Fig. 4) using biolayer Interferometry (BLI) with an Octet RED96e system (FortéBio)30. hACE2 was used as a positive control (Fig. 4a).
Even though this technique presents some drawbacks31 offering narrow signal windows with low molecular weight analytes32 such as peptides, it remained useful to identify and rank our binding mimics. In the conditions tested here, peptide P1 does not bind to RBD when using 100 nM nor 10 µM peptide solutions (Fig. 4b). For peptides P8, P9, and P10, multiple concentrations experiments were performed and dose-dependent associations were observed (Fig. 4c–e). Of note, only association rates could be quantified accurately, the dissociation ones being very slow, highlighting strong binding properties for these mimics (Supplementary Table 6).
The current pandemic originated by SARS-CoV-2 causes an unprecedented health crisis. The medical world has found itself helpless in the face of this virus, having to deal with the absence of specific effective treatment. At the time of writing, preventive vaccines are not yet clinically approved, other antiviral drugs have been shown ineffective, and specific drugs addressing SARS-CoV-2 targets are lacking4. Among all possible viral targets, the virus spike protein/hACE2 interaction has been validated and the design of compounds able to block this interaction upon binding to spike protein is a promising approach. However, developing a specific drug at a pandemic speed is a hard task especially in the design of a small molecule. Indeed, beyond the time required for the identification and validation of a lead compound after a library screening, followed by structure-activity relationship studies and clinical development, small molecule drugs are associated with a high attrition rate partly due to their off-target toxicity observed during pharmacological studies.
Peptides appear here as a possible solution for design and development at pandemic speed. Peptides are widely recognized as promising therapeutic agents for the treatment of various diseases such as cancer, and metabolic, infectious, or cardiovascular diseases33,34,35. To date, ~70 peptide drugs have reached the market and 150 are currently under clinical development33,36. Special advantages that peptides show over small drugs include their high versatility, target-specificity, lower toxicity, and ability to act on a wide variety of targets35 which are directly responsible for a greater success rate than small molecules (approval rate of around 20% versus 10%)36,37. The synthesis and the development of long therapeutic peptides (over 30 residues) are no longer a challenge, as highlighted by the success story of many GLP-1 analogs38. Their possible antigenicity can be evaluated using prediction tools in the design20.
Of course, even for peptides, the development of a drug at a pandemic speed requires some considerations. Our aim was to design a peptide with reasonable helical folding propensity in water in order to mimic the H1 helix of hACE2 in the protein context, considering that this helical folding is a prerequisite to compete with hACE2 upon interaction with viral spike protein. The design was realized using only natural amino acids15 and avoided complex tools that are known and validated to stabilize α-helix16. Stabilizing α-helical structure of medium-sized peptide sequences (up to 15 residues) using only natural amino acids is a hard but achievable task39. Our choice was guided by the desire to build a simple peptide that can be upscaled quickly and easily, without technical constraints that may require laborious development. We also assumed that the use of mostly natural amino acids can facilitate the essential stages of the development of therapeutic tools in the event of success, particularly concerning pharmacokinetics, preclinical, and clinical toxicity aspects. We thought it would be a fair compromise between designing α-helix peptides with optimized binding affinity and developing an effective tool within short deadlines while integrating the constraints of developability to move a prophylactic device and/or a therapeutic peptide drug quickly in the clinic.
Using a combination of validated methods, we improved the helical folding propensity of the native α-helix extracted from the protein context. Thanks to leucine and alanine scanning (Table 1 and Supplementary Tables 2 and 3) a first set of peptides (P1 to P8) were designed and synthesized. These peptides demonstrated to have a high helical content (up to 80% for P6). However, increasing this helical content to a maximum level led to increasing mean hydrophobicity and a hydrophobic moment (Supplementary Table 4) that proved to be detrimental to solubility and efficacy. The substitution of a leucine residue by the homotyrosine residue led to the peptide analog P7 with a slight increase in solubility and a weak efficiency to block SARS-CoV-2 cell infection. In this first generation of peptides, the 27-residue P8 peptide appeared to be highly soluble with a high helical folding propensity (70%), and an ability to block SARS-CoV-2 cell infection at 10 μM on Vero-E6 cells (Fig. 3a).
In order to improve the potency of our peptides, we designed a second set of mimics combining the properties of peptides P7 and P8, i.e., P9 and P10. If the Leu/hTyr substitution led to a slight decrease in helicity, this was at the advantage of the mean hydrophobicity (Supplementary Table 4) also highlighted by lower HPLC retention times (Supplementary Table 5 and Supplementary Data 1). These peptides proved to be highly efficient in reducing SARS-CoV-2 viral titers (100% efficacy at 1 µM) on pulmonary cells with an IC50 in the nanomolar range. This blocking property is related to their ability to bind to SARS-CoV-2 spike RBD with affinity estimated in the sub-nanomolar range (Table 1 and Supplementary Table 6). Finally, these peptides proved to be devoid of cell toxicity at 150 times the IC50 concentration (Fig. 3c, f) highlighting their therapeutic potential.
In conclusion, we demonstrated here the feasibility of designing hACE2 peptide-mimics with high helical folding propensity in water. The folding propensity promotes interaction with spike RBD and blocks SARS-CoV-2 pulmonary cell infection. Devoid of cell toxicity even at high doses, these mimics could be considered for prophylactic or therapeutic purposes upon adequate formulation. Targeting prophylaxis first might shorten the drug development time scale. Delivered through a medical device such as a nasal or oral spray or as a sublingual tablet, these peptides could be aimed at blocking the infectivity of the virus in a preventive manner. Their biodistribution would be limited to the upper airways (nasal and oral cavity) before they are degraded in the digestive tracks without toxic residues. Their therapeutic use might also be considered formulated in that case as an inhaler to reach pulmonary cells.
Peptides were produced manually, synthesized from Fmoc-protected amino acids utilizing standard solid-phase peptide synthesis methods. Solid-phase peptide syntheses were performed in polypropylene Torviq syringes (10 or 20 mL) fitted with a polyethylene porous disk at the bottom and closed with an appropriate piston. Solvent and soluble reagents were removed through back-and-forth movements. The appropriate protected amino acids were sequentially coupled using PyOxim/Oxyma as coupling reagents. The peptides were cleaved from the rink amide resin with classical cleavage cocktail trifluoroacetic acid/triisopropyl silane/water (95:2.5:2.5). The crude products were purified using preparative scale high-performance liquid chromatography (HPLC). The final products were characterized by analytical liquid chromatography (LC)–mass spectrometry (MS). All tested compounds were trifluoroacetic acid salts and were at least 95% pure. The relevant peptides after CD spectra analyses were selected and produced by Genecust France on 20 mg scale.
Preparative scale purification of peptides was performed by reverse phase HPLC on a Waters system consisting of a quaternary gradient module (Water 2535) and a dual wavelength UV/visible absorbance detector (Waters 2489), piloted by Empower Pro 3 software using the following columns: preparative Macherey-Nagel column (Nucleodur HTec, C18, 250 mm × 16 mm internal diameter, 5 μm, 110 Å) and preparative Higgins analytical column (Proto 200, C18, 150 mm × 20 mm i.d., 5 μm, 200 Å) at a flow rate of 14 mL min−1 and 20 mL min−1, respectively. Small-scale crudes (<30 mg) were purified using semipreparative Ace column (Ace 5, C18, 250 mm × 10 mm i.d., 5 μm, 300 Å) at a flow rate of 5 mL min−1. Purification gradients were chosen to get a ramp of ~1% solution B per minute in the interest area, and UV detection was done at 220 and 280 nm. Peptide fractions from purification were analyzed by LC−MS (method A or B depending on retention time) or by analytical HPLC on a Dionex system consisting of an automated LC system (Ultimate 3000) equipped with an autosampler, a pump block composed of two ternary gradient pumps, and a dual wavelength detector, piloted by Chromeleon software. All LC−MS or HPLC analyses were performed on C18 columns. The pure fractions were gathered according to their purity and then freeze-dried using an Alpha 2/4 freeze-dryer from Bioblock Scientific to get the expected peptide as a white powder. Final peptide purity (>95%) of the corresponding pooled fractions was checked by LC−MS using method A (outlined below).
Two methods were conducted for LC−MS analysis. Method A. Analytical HPLC was conducted on a X-Select CSH C18 XP column (30 mm × 4.6 mm i.d., 2.5 μm), eluting with 0.1% formic acid in water (solvent A) and 0.1% formic acid in acetonitrile (solvent B), using the following elution gradient: 0−3.2 min, 0−50% B; 3.2 − 4 min, 100% B. Flow rate was 1.8 mL min−1 at 40 °C. The mass spectra were recorded on a Waters ZQ mass spectrometer using electrospray positive ionization [ES + to give (MH) + molecular ions] or electrospray negative ionization [ES−to give (MH) − molecular ions] modes. The cone voltage was 20V. Method B. Analytical HPLC was conducted on a X-Select CSH C18 XP column (30 mm × 4.6 mm i.d., 2.5 μm), eluting with 0.1% formic acid in water (solvent A) and 0.1% formic acid in acetonitrile (solvent B), using the following elution gradient: 0−3.2 min, 5−100% B; 3.2−4 min, 100% B. Flow rate was 1.8 mL min−1 at 40 °C. The mass spectra were recorded on a Waters ZQ mass spectrometer using electrospray positive ionization [ES+ to give (MH)+ molecular ions] or electrospray negative ionization [ES− to give (MH)− molecular ions] modes. The cone voltage was 20 V.
CD spectra were recorded on a Jasco J-815 CD spectropolarimeter equipped with a Peltier temperature controller. Data were obtained at 25 °C over a wavelength range between 185 nm and 270 nm, using a wavelength interval of 0.2 nm and a scan rate of 20 nm min−1. Peptide samples were prepared at a concentration of 60 µM in 50 mM sodium phosphate buffer, pH 7.4, in a quartz cell of 1 mm path length. CD experiments were processed and plotted with R program. CD spectra were analyzed using DICHROWEB web server and CDSSTR deconvolution algorithm24.
Anti-infectivity study on Calu-3 and Vero-E6 cells
Cells and virus preparation
Calu-3 (ATCC HTB55) and Vero-E6 (ATCC CRL-1586) cells were purchased from the American Type Culture Collection and routinely checked for mycoplasma contamination26. Cells were cultured in Dulbecco’s Modified Eagle Medium (DMEM) supplemented with non-essential amino acids, penicillin-streptomycin, and 10% v/v fetal bovine serum.
The SARS-CoV-2 clinical isolate was obtained from BAL of a symptomatic infected patient (#SARS-CoV-2/PSL2020, available at Pitié-Salpêtrière hospital, Paris (France)). The patient recruited for virus isolation and culture was in intensive care unit in the Pitié Salpêtrière hospital. The patient underwent a bronchoalveolar lavage for clinical purpose (seeking for a bacterial pulmonary infection). The protocol was approved by our institution’s ethics committee (Immuno-COVID-REA, CER-Sorbonne Université, no. CER-SU-2020-31). BAL (0.5 mL) was mixed with an equal volume of DMEM without FBS, supplemented with 25 mM Hepes, double concentration of penicillin–streptomycin and miconazole (Sigma), and added to 80% confluent Vero-E6 cells monolayer seeded into a 25-cm2 tissue culture flask. After 1 h adsorption at 37 °C, 3 mL of infectious media (DMEM supplemented with 2% FBS, penicillin-streptomycin and miconazole) were added. Twenty-four hours post-infection another 2 mL of infectious media were added. Five days post-infection, supernatants were collected, aliquoted, and stored at −80 °C (P#1). For secondary virus stock, Vero-E6 cells seeded into 25 cm2 tissue culture flasks were infected with 0.5 mL of P#1 stored aliquot, and cell-culture supernatant were collected 48 h post-infection and stored at −80 °C (P#2). Infectious viral particles were measured by a standard plaque assay previously described25 with fixation of cells 72 h post infection. Accordingly, the viral titer of SARS-CoV-2/PSL2020 P#2 stock was about 5.3 105 PFU mL−1.
Vero-E6 or Calu-3 (1 × 105 cells mL−1) were seeded into 24 wells plates in infectious media and treated with different concentrations of the peptides (from 0.1 to 10 μM). After 30 min at room temperature, cells were infected with 0.1 multiplicity of infection (MOI) (Vero-E6) or 0.3 MOI (Calu-3) of SRAS-CoV-2 (SARS-CoV-2/PSL2020 P#2 stock) in infectious media. Cell supernatants were collected at 48 h post-infection for enzyme-linked immunosorbent assay (ELISA) assay using a SARS-CoV-2 (2019-nCoV) nucleoprotein ELISA kit (Sino biological), according the manufacturer’s instructions, and standard plaque assay26. Inhibition of infection was calculated comparing viral concentration in each case with that of untreated SARS- CoV-2-infected cells.
Toxicity study on Calu-3 and Vero-E6 cells
Cell cytotoxicity was measured using MTT assays and fluorescent activated cell sorting (FACS). Calu-3 and Vero-E6 were seeded in 96-well (for MTT assays) or 24-well (for FACS) plates and let adhere. When ~40% confluence was reached, the wells were washed, and new medium containing vehicle (water, 5% final volume) or different concentrations of the indicated peptide was added. MTT (2 mM) was added to each well after 24 h, 48 h, or 72 h of treatment and incubated 4 h at 37 °C. Supernatants were then discarded and formazan salts were dissolved in DMSO to read plate absorbance at 570 nM. Absorbance in each well was normalized with those treated with vehicle. For FACS analyses, cells were harvested from the wells with the help of accutase, pelleted, and stained with Annexin-V-APC (0.1 μg mL−1) and propidium iodide (0.5 µg mL−1) in annexin binding buffer (10 mM Hepes pH 7.4, 140 mM NaCl, and 2.5 mM CaCl2). Cells were sorted in a FACScalibur flow cytometer and data was analyzed using FlowJo 10.0 software, considering cell death as the sum of Ann-V+/PI− and Ann-V+/PI+ events.
Biolayer Interferometry experiments
Fc-tagged 2019-nCoV RBD-SD1 (Sanyou Biopharmaceuticals Co. Ltd) was immobilized to an anti-human capture sensortip (FortéBio) using an Octet RED96e (FortéBio). The sensortip was then dipped into 100 nM hACE2 (Sanyou Biopharmaceuticals Co. Ltd, His Tag) or 1 µM of any tested peptide to measure association before being dipped into a well containing only running buffer composed of DPBS (Potassium Chloride 2.6 mM, Potassium Phosphate monobasic 1.5 mM, Sodium Chloride 138 mM, Sodium Phosphate dibasic 8 mM), 0.05% Tween 20 and 0.5% bovine serum albumin to measure dissociation. (Extended conditions, and suppliers in Supplementary Note 1).
Statistics and reproducibility
All conditions in the viral neutralization and cell cytotoxicity experiments were tested in triplicate. Data from viral neutralization assays was analyzed using nonlinear regression, fitting sigmoidal curves used to calculate the IC50 values with Graphpad Prism 8.0.1. For BLI experiments, data were reference subtracted and fit to a 1:1 binding model using Octet Data Analysis Software v10.0 (FortéBio). KD values were extracted from 3 independent determinations (P9 and P10) validated by a statistical coefficient determination (R2) > 0.95.
Further information on research design is available in the Nature Research Reporting Summary linked to this article.
The complex between hACE2 and the surface spike protein of SARS-CoV-2 data used for peptide design is available in RCSB PDB with the identifier doi: 10.2210/pdb6M0J/pdb14. The randomly selected RBD amino-acid sequences from China (QOH25833, QIG55857, QHR63290, QHR63250, QJG65957, QJG65956, and QJG65951), USA (QIV65044, QJD23847, QJU11481, QJD24531, QJD25193, QJD25529, and QJA17180), and France (QJT73034, QJT73010, QJT72902, QJT72806, QJT72794, QJT72722, QJT72710, QJT72626, QJT72614, and QJT72554), used for sequence alignment are available in the Genebank database at ncbi.nlm.nih.gov. The amino acid sequence of the Fc-tagged 2019-nCoV RBD-SD1 was provided by Sanyou bio with purchase (sanyoubio.com/EN/2019-nCoV.php) and is depicted in Supplementary Fig. 1a. The datasets generated and/or analyzed during the current study are in the manuscript and the raw data are available from the corresponding author on reasonable and justified request.
The predictive data supporting our work was generated using publicly available software. For sequence alignment, the Weblogo software (available at https://weblogo.berkeley.edu) and Clustal Omega (available at https://ebi.ac.uk/Tools/msa/clustalo/) were used. The Agadir helical content predictor is available at https://agadir.crg.es. Peptide antigenicity can be determined at https://imed.med.ucm.es/Tools/antigenic.pl. Online analysis for peptide CD spectra and using DichroWeb server and the CDSSTR algorithm is available at https://dichroweb.cryst.bbk.ac.uk. The HELIQUEST web server used to calculate peptide hydrophobicity and hydrophobic moment is available at https://heliquest.ipmc.cnrs.fr.
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This work was supported by private funds (P.K.), SATT-Lutech, Kaybiotix (LGM PhD grant), and French Research Ministry (EO PhD grant). P.K. is grateful to SATT-Lutech team supporting this project, to Fabrice Viviani and Akanksha Gangar from Oncodesign for their unwavering support. The authors thank David Boutolleau from the Virology Department, Pitié-Salpêtrière, AP-HP, where was diagnosed the BAL SARS-COV-2 infection. Philippe Karoyan dedicates this work to Gérard Chassaing on the occasion of his 75th birthday. “There are no borders in science. The only limit is our imagination.”
The authors declare the following competing financial interest(s): The patent application EP20305449.9 included results from this paper.
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Karoyan, P., Vieillard, V., Gómez-Morales, L. et al. Human ACE2 peptide-mimics block SARS-CoV-2 pulmonary cells infection. Commun Biol 4, 197 (2021). https://doi.org/10.1038/s42003-021-01736-8
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