Self-assembling virus-like particles represent highly attractive tools for developing next-generation vaccines and protein therapeutics. We created ADDomer, an adenovirus-derived multimeric protein-based self-assembling scaffold nanoparticle engineered to facilitate plug-and-play screening of multiple immunogenic epitopes from pathogens. We used cryo-electron microscopy at near-atomic resolution and implemented novel, cost-effective, high-performance cloud computing to reveal architectural features in unprecedented detail. We analyzed ADDomer interaction with immune components and developed a promising first-of-kind ADDomer-based vaccine candidate to combat emergent Chikungunya infectious disease, exemplifying the potential of our approach.
Self-assembling protein-based nanoparticles are highly attractive tools for a wide range of biomedical applications, including vaccine development and cancer therapy (1–4). Present in all kingdoms of life, they form supramolecular architectures with unique properties (4), including spontaneous self-organization from simple precursor protomers amenable to engineering. Moreover, particle size is generally in the range of pathogens, notably viruses, which the immune system has evolved to strongly react against (5, 6). Protein-based nanoparticles often adopt quasi-spherical shapes encapsulating a central cavity that can carry cargo, rendering them suitable for drug delivery (3). Virus-like particles (VLPs) are made of many copies of identical building blocks resulting in highly repetitive surfaces, providing opportunities to display pathogen-derived epitopes. These are often oligopeptide sequences, on their own generally not immunogenic enough to elicit a strong immune response resulting in protection (5, 6). However, if coupled to self-assembling protomers forming the VLP, then peptide epitopes can reach very high densities on the VLP, potentially capable of triggering B cell receptor clustering and cross-presentation for facilitation of a strong immune response (5, 7). Notably, VLPs can act as self-adjuvants, alleviating the need for additional vaccine formulations with additional adjuvanting reagents that may have undesired side effects (8).
VLPs are extensively researched for new and better vaccines and therapies against acute and chronic diseases (2, 3, 9–11). An ideal VLP-based vaccine would be safe, free of nucleic acid contaminants, capable of engineering, well produced recombinantly, easy to purify, available in large quantities, self-adjuvanting, and capable of eliciting a strong immune response to pathogen-derived antigens. presented in a native conformation at high density on the particle surface. One major aspect is thermotolerance — many vaccines today require refrigeration, storage and deployment dependent on a cold chain function, posing problems in remote or less affluent regions (12). Thus, thermostability would be a highly advantageous asset for any VLP vaccine.
Human adenoviruses are among the most widely used vectors in gene therapy (13). The icosahedral adenovirus capsid comprises distinct proteins arranged in hexons, pentons, and fiber extrusions. The penton-forming protomer of certain adenovirus serotypes can self-assemble into a symmetric, hollow dodecahedron adopted by 12 pentons comprising altogether 60 protomers (14), effectively representing a proteinaceous, nonenveloped VLP. We have shown previously that human adenovirus serotype 3 (Ad3) dodecahedron can be produced in baculovirus-infected insect cells (15) and can retain the adenovirus-like ability to penetrate epithelial cells (16). We studied the structure and mechanism of Ad3-derived dodecahedron, investigating its potential as a delivery system for DNA, proteins, and chemical compounds (17–19). Encouraged by these promising proof-of-concept results, we set out to create a synthetic, engineered Ad3-derived stable dodecahedron-forming protomer for highly efficient multiepitope display and delivery to a next-generation ADDomer VLP platform for vaccines and protein therapeutics.
ADDomer multiepitope display and delivery platform
Comparison of primary sequences of penton-forming promoters from many adenovirus serotypes revealed particularly two regions of high variability in length and sequence, called variable loop (VL) and arginine-glycine-aspartic acid (RGD) loop. For instance, VL comprises 20 amino acids in Ad3 while only 9 amino acids in Ad41. RGD loop plasticity is even more pronounced in Ad12, spanning 11 residues, in contrast to 74 residues in Ad2. The VL has previously been shown to accommodate an influenza-derived immunogenic eptitope (20). The RGD loop contains a conserved tripeptide motif (-RGD-) mediating integrin-based internalization into target cells (21). We reasoned that these VL and RGD loop regions, given their polymorphism, would be ideally suited to accommodate one or several antigenic epitopes each. Therefore, we redesigned the protomer-encoding gene adopting a “BioBrick” format (22) to facilitate multiple epitope insertions. We inspected the crystal structure of Ad3 dodecahedron (17) and identified suitable loci adjacent to secondary structure motifs flanking the loops. The RGD loop in wild-type Ad3 is much more extended than the VL. As tripeptide is important for cell internalization, we decided to split the RGD loop into two sections before and after the RGD motif, which we kept unaltered. We inserted unique restriction sites to create three independent loci for epitope display, one in VL and two in the RGD loop to facilitate the insertion of synthetic DNAs encoding for antigenic epitopes of choice in the resulting plug-and-play multiepitope display platform, the ADDomer (Fig. 1A and figs. S1 and S2). We expressed ADDomer using MultiBac, the baculovirus / insect cell system we developed for complex protein biologics (23), resulting in highly purified ADDomer (fig. S1) with excellent culture yields (50 mg from a 50-ml culture) and negligible nucleic acid or endotoxin contamination.
ADDomer structure and mechanism
Unlocking ADDomer to future structure-based design, we determined its molecular architecture by high-resolution cryo-electron microscopy (cryo-EM) (Fig. 1, B to H, and figs. S3 and S4). For parts of the process, we use public cloud resources, image processing and refinement software for this purpose. Our cryo-EM structure, at up to 3.2-Å resolution, reveals ADDomer adopts the familiar dodecahedron, formed by 12 pentons in a quasi-spherical arrangement, with the RGD loop and VL densely decorating the particle surface (Fig. 1, B and C, fig. S3, and table S1). Our structure shows that the plasticity of the RGD loop and VL, essential for antigenic epitope presentation, is maintained in the ADDomer (Fig. 1D).
Crystal structures of wild-type Ad3 dodecahedron with and without bound peptide fiber exist at lower resolution (3.8 and 4.8 Å, respectively) (17). Close inspection of our cryo-EM structure reveals notable differences. The fiber-binding cleft adopts a rearranged conformation, apparently between the geometries observed in the crystals of the apo- and fiber-bound Ad3 dodecahedron (Fig. 1E) (17). The protomer represents a two-domain architecture, with a crown region comprising the VL and RGD loop abutting a jellyroll fold mediating multimerization (Fig. 1, D and F). In our cryo-EM structure, we observed additional density between the crown and jellyroll domains, juxtaposed to four sulfur-containing amino acids (M131, M138, M458, and C539), consistent with a tetradentate coordination by a metal ion, possibly zinc or iron (Fig. 1F). We posit that a metal ion structure at this interdomain interface could be important for stabilizing this fold protein.
In the Ad3 dodecahedron crystal, a Ca2+ occupied ion of a central cavity lined by glutamates (E466) in α-helices from different protomers (Fig. 1G). No corresponding density is observed by cryo-EM. The Ad3 crystallization conditions contained CaCl2, while we did not supplement Ca2+ during the ADDomer purification to occupy this site. Consequently, glutamates E466 do not extend into the cavity, but the corresponding α-helices are slightly shifted in the ADDomer.
A hallmark in the Ad3 crystal structure was strand-swapping between extended N-terminal regions of neighboring protomers, considered essential to dodecahedron structural integrity (17). Unexpectedly, we did not observe this strand-swapping by cryo-EM (Fig. 1H and fig. S4C). Rather, in the ADDomer, two neighboring protomers engage in hydrogen bonds in the vicinity of the twofold axis, extending from the S61 side chain to the E59 backbone peptide and vice versa. We can exclude that the observed differences are due to ADDomer amino acid additions and substitutions within the VL and RGD loop, as they are in the crown domain and thus sterically too distant to have a bearing on the N-terminal domain, or the formation of the hitherto unobserved metal binding site, respectively.
Strand-swapping and Ca2+ ions would conceivably stabilize the dodecahedron. We didn't observe either of these features by cryo-EM and thus wondered about ramifications for ADDomer stability. Thermal shift assays evidenced a melting temperature of 54 ° C for the ADDomer and no noticeable melting below 45 ° C (fig. S5A). We challenged ADDomer integrity by storing for weeks at room temperature, freezing and thawing, and incubating at 45 ° C. Negative-stain EM revealed a uniformly stable ADDomer (fig. S5, B to E). Thus, we can conclude that ADDomer maintains highly advantageous thermotolerance, begging the question of exactly what the source of this remarkable stability may be.
ADDomer (30 nm) is within the size range (20 to 200 nm) of particles readily drained to lymph nodes, potentiating uptake by antigen-presenting cells and cross-presentation (5, 6). We analyzed ADDomer uptake by human cells, including monocytes and monocyte-derived dendritic cells (MDDCs), confirming efficient internalization (Fig. 2, A and B). We next investigated lymph node distribution in mice injected with fluorescently labeled ADDomer (Fig. 2, C and D). Rapid draining to the right inguinal lymph node was observed irrespective of the mode of administration. No signal was found in the opposite left inguinal node serving as internal control. Mesenteric and axillary nodes evidenced rapid but not lasting signal (Fig. 2D). Our results underscore ADDomer's ability to drain rapidly to the nearest lymph node and efficiently penetrate human cells, including antigen-presenting lymphocytes.
Engineering ADDomer to combat emergent infectious diseases
Infectious diseases continue to decimate populations worldwide, and among our means to combat this threat, vaccination is extremely powerful. Recent examples that dominate the media are Chikungunya and Zika infectious diseases, transmitted by mosquitoes originally confined to sub-Saharan Africa but increasingly spreading to the Northern Hemisphere. We used our plug-and-play setup to rapidly generate ADDomers displaying multiple copies of immunogenic epitopes from a range of human and livestock viral pathogens, testing the capacity of the insertion loci in the process (fig. S6 and table S2). To evaluate the flexibility of the ADDomer to harbor large multiepitope insertions, we combined five immunogenic Gumboro-derived epitopes in tandem. Gumboro is caused by infectious bursal disease virus and affects poultry, causing significant economic shortfall, especially in developing countries. ADDomer evidenced remarkable plasticity for insertion of the five tandem Gumboro-derived epitopes in both functionalized VL and RGD loop without compromising integrity (fig. S6, A and B). Insertion in the VL evidenced a blurring of the penton edges, suggesting preferred orientations of the loop structure comprising the Gumboro epitopes. Notably, we successfully inserted an epitope test exceeding 200 amino acid residues in the RGD loop (fig. S6B). Together, our data demonstrates the full functionality of the insertion loci we engineered and conveyed that long sequences containing multiple epitopes can be efficiently displayed at high density on the ADDomer.
Notably, the sera of most patients suffering from Chikungunya viral infection react with a specific linear peptide, E2EP3 (24). This major neutralizing epitope is located at the very N terminus of the viral E2 glycoprotein, comprising the first 18 amino acids (Fig. 3A and table S2). We inserted E2EP3 into ADDomer to create a VLP vaccine candidate, ADDomer-tevCHIK, with the potential to combat this debilitating disease. To recapitulate the exposed conformation of E2EP3 in Chikungunya virus, we inserted a site for a highly specific protease [tobacco etch virus (TEV) NIa] right in front of the epitope, which, upon cleavage, generates a native-like conformation comprising an exposed N-terminal serine (Fig. 3A). Processing by TEV results in quantitative cleavage (Fig. 3B). Negative-stain EM confirmed that, impressively, the ADDomer dodecahedron remained intact notwithstanding multiple (60-fold) polypeptide backbone cuts (Fig. 3C). Immunization experiments compellingly validate our approach. Uncut ADDomer-tevCHIK did not yield E2EP3-specific immunoglobulin titers (fig. S7). In contrast, quantitatively cleaved ADDomer-tevCHIK native E2EP3-like exposure elicited very strong specific immunoglobulin G (IgG) response with barely detectable IgM (Fig. 3D and figs. S7 and S8), in excellent agreement with the immune response to viral Chikungunya. infection. An unrelated nanoparticle scaffold made of polylactic acid harboring the same amount of CHIK peptide epitopes did not result in an immune response above background in mice, suggesting that the scaffold ADDomer itself may have an adjuvanting effect (fig. S7).
In summary, we present here ADDomer, our plug-and-play multiepitope display platform for antigenic epitopes from various origins, including emerging human viral pathogens or veterinary infectious diseases. We determined ADDomer architecture at near-atomic resolution by cryo-EM, enabled by a heterogeneous computing cluster and created and executed automatically with public cloud infrastructure. Our approach presents a novel, fast, and cost-effective general mechanism to quickly analyze and process cryo-EM data and sets the stage for comprehensive (re) design of the ADDomer particle, as well as fine-tune self-adjuvanting potential by modulating sequences. plasticity (25). ADDomer is easy to modify and produce in high yields using our recombinant system. It is remarkably thermostable, which could render the employment of ADDomer-based vaccines independent of a cold chain, a crucial asset. We demonstrate that ADDomer rapidly drives to lymph nodes and efficiently internalizes immune blood cells. We inserted multiepitope sequences exceeding 200 amino acids without compromising ADDomer integrity, conveying that even folded domains or entire proteins could be displayed. ADDomer can be cleaved multiple times in loops without adverse effects, enabling native-like display of adopted conformational epitopes, compellingly demonstrated here with Chikungunya E2EP3. Notably, modification of the ADDomer is not restricted to the engineered loci. The fiber binding cleft could also be used to attach peptides and proteins, tagged with fiber peptide. Moreover, the N-terminal extension was shown to react with specific binding domains (19), conferring further capacity. Thus, the ADDomer can accommodate hundreds of epitopes, same or different, providing a great opportunity for combinatorial display by a single particle (fig. S9). Last, the central cavity within the ADDomer could be used to encapsulate costimulatory molecules. We anticipate that a wide range of applications in biomedical research will benefit from this exceptionally versatile display platform.
MATERIALS AND METHODS
We used the penton base protein from human Ad3 (GenBank Z29487) as a starting point and implemented a BioBrick format (22) to functionalize one locus within the VL and two loci in the RGD loop for facile and rapid custom DNA insertion (fig. S1). The insertion loci were flanked by unique restriction sites that were eliminated elsewhere in the Ad3 penton base gene encoding. To preserve the structural integrity of the penton base protein, the restriction sites were designed in silico to be located outside and adjacent to known secondary structural elements in the penton base protein. The resulting gene encoding for ADDomer was synthesized, codon-optimized for recombinant expression, and pasted into plasmid pACEBac1 (Geneva Biotech SARL, Switzerland) (26) using Bam HI and Hind III restriction sites, giving rise to pACEBac-ADDomer. The primary sequence of the encoded ADDomer is provided in fig. S2. In this study, the pACEBac-ADDomer served as the backbone for inserting DNA encoding for selected epitopes into the designed insertion loci in variable and RGD loops. Primary sequences of the inserted epitopes in this study are listed in table S2.
Expression and purification
pACEBac-ADDomer and epitope-displaying variants were expressed using the MultiBac baculovirus expression system we developed (fig. S1) (23). Briefly, pACEBac-ADDomer and variant plasmids were inserted by Tn7 transposition into an engineered baculoviral genome, EMBacY, in DH10EMBacY cells (27). Transfection, baculovirus amplification, storage, and protein expression in Hi5 insect cell suspension cultures (50 ml) were performed following established protocols (27), resulting in exceptional yields (fig. S1). The EMBacY baculoviral genome encodes a yellow fluorescent protein (YFP) marker. When the YFP signal reached a plateau, cells were harvested by centrifugation, and the pellets were flash-frozen in liquid nitrogen and stored at −20 ° C. Pellets were resuspended in hypotonic lysis buffer[033×phosphate-bufferedsaline(PBS);1mlper25×10[033×phosphate-bufferedsaline(PBS);1mlper25×107 cells]supplemented by EDTA-free cOmplete protease inhibitor (Roche, Switzerland) and lysed by three cycles of freezing and thawing. Lysate was purified from debris by centrifugation (6000g for 30 min), and the purified supernatant was subjected to sucrose gradient (15 to 40%) centrifugation (15). Fractions containing ADDomer (30 to 40% sucrose) were pooled and dialyzed against buffer A [10 mM Hepes (pH 7.4) and 50 mM NaCl]. The addomer was further purified by ion exchange chromatography using a High Q column (Bio-Rad) using buffer A and applying a linear salt gradient (50 to 500 mM NaCl). Fractions containing highly purified ADDomer (330 to 400 mM NaCl) were pooled and stored at ambient temperature or frozen (−80 ° C). For animal studies, ADDomer particles were further purified using Detoxi-Gel (Thermo Fisher Scientific) to remove endotoxins, followed by dialysis against PBS.
Following purification, absorbance spectroscopy measurement showed an OD260nm (optical density at 260 nm) / OD280nm ratio below 0.6, evidencing lack of nucleic acid contamination. Before injection into mice, endotoxin levels were quantified using Endosafe PTS (Charles River) evidencing 754 EU (endotoxin units) / mg for ADDomer-tevCHIK and 247 EU / mg for ADDomer, respectively. In our injections, we were thus below 30 EU, the common cutoff value for testing adjuvant properties of any recombinant antigen in a mouse model.
Highly purified ADDomer sample was stored in PBS at room temperature. Thermal shift experiments were performed at an ADDomer concentration of 3 mg / ml in PBS, using a ThermoFluor assay (28). The ADDomer sample was diluted to 1 mg / ml and aliquoted. Identical sample aliquots were stored for several weeks at room temperature, frozen at −20 ° C overnight followed by thawing, and incubated at 45 ° C for 1 hour, respectively. Sample integrity was assessed at each intervention by negative-stain EM (fig. S5).
Negative-stain EM was performed with purified ADDomer (0.1 to 0.5 mg / ml) dialyzed into 25 mM Hepes (pH 7.5), 150 mM NaCl, and 2 mM EDTA. The sample was stained with 3% uranyl acetate. Micrographs were recorded using a 200-kV FEI Tecnai T20 microscope with an Eagle 4k × 4k charge-coupled camera device.
Cryo-EM and data collection
Five microliters of purified ADDomer (0.1 mg / ml) was applied to glow-discharged holey carbon grids (Quantifoil, R 2/2 300 mesh). Samples were incubated on the grid for 2 s and blotted for 0.4 s at 90% relative humidity and 18 ° C inside a Leica EM GP, before plunge-freezing in liquid ethane. Cryo-EM data were collected at 200 kV with a FEI Talos Arctica microscope equipped with a Gatan K2 direct electron detector and an energy filter using automated acquisition software (EPU). A total of 1060 dose-fractionated films each containing 32 frames (0.25 s per frame) with an accumulated total dose of 42 e–/ Å2 were recorded at a nominal magnification of × 130,000 corresponding to a pixel size of 1.06 Å. Images were recorded with a defocus range of −0.8 to −3.2 μm (table S1).
Image processing was performed with the RELION 2.1 software package (29). The micrographs were motion-corrected using MotionCorr2 (30), and contrast transfer function (CTF) information was determined using ctffind4.1 (31). Together, 262 micrographs with CTF rings extending beyond 4.6 Å were selected for further processing. A total of 3600 particles were boxed using RELION autopicking software. After two-dimensional (2D) classification (fig. S3C) and 3D classification with imposed icosahedral symmetry, initial 3D autorefinement led to a reconstruction of ~ 4.2-Å resolution. Further rounds of 3D classification / refinement were carried out on polished particles before using postprocessing for masking and automatic B factor sharpening. The resolution of the final map was determined to be 3.5 Å based on the Fourier shell correlation (FSC) 0.143 cutoff criterion (fig. S3D) (32). Local resolution was calculated using the local resolution estimation program in RELION (fig. S3E).
Processing and 3D classification of ADDomer were performed using public cloud resources provided by Oracle Cloud Infrastructure. Using this rather than an institutional cluster allows a faster turnaround time of analysis. Because of the specific nature of the computational work performed by the steps within RELION, a heterogeneous cluster was prepared with both a central processing unit (CPU) – and a graphical processing unit (GPU) – focusing resources. A pipeline of workloads was created, allowing work best suited to each compute type to use only the resources needed and automatically release compute resources when no longer needed. This permits parts of the workflow to use lower-cost CPU resources and burn to GPU only for those parts that would benefit from GPU optimization, reducing overall cost while increasing total data throughput. The total cost to run the image processing pipeline on the cloud was approximately £ 200.
Model building and refinement
Homology modeling was performed using I-TASSER (33) using the human adenovirus Ad3 structure as template (17). The model was adjusted to fit into the map manually using COOT (34) before further iterative positional and B factor refinement in real space using Phenix Real-Space refinement software (35). Final adjustments were made in COOT before evaluating the model using MolProbity (36). Refinement statistics are summarized in table S1.
Cell culture and differentiation
HeLa cells were cultured in Dulbecco's modified Eagle's medium supplemented with 10% fetal calf serum (FCS) (Thermo Fisher Scientific) at 37 ° C under 5% CO.2. Monocytes were purified by centrifugation on Ficoll (Sigma-Aldrich) for 20 min at 800g, and mononucleated cells were subsequently passed through EasySep magnetic beads (STEMCELL Technology). Monocyte purity was verified by flow-cytometry by means of CD14 labeling. MDDCs were generated by culturing monocytes in RPMI 1640 FCS medium supplemented with granulocyte-macrophage colony-stimulating factor at 100 ng / ml and interleukin-4 at 25 ng / ml for 6 days. Differentiation to MDDCs was verified by FACS based on CD14 / CD209 labeling.
HeLa cells were grown on glass coverslip and incubated for 1 hour at 37 ° C with unlabeled ADDomer at 20 μg / ml. Subsequent to methanol fixation, rabbit serum raised against human Ad3 penton base protein, diluted 1: 1000 in PBS, was applied, followed by Cy5-labeled goat anti-rabbit antibody (Jackson ImmunoResearch), diluted 1: 500 in PBS. Nuclei were stained by DNA dye 4 ′, 6-diamidino-2-phenylindole.
Monocytes and MDDCs from healthy anonymous donors were obtained from the National Blood Service [Etablissement Francais du Sang (EFS), La Tronche] after written consent following approval by the EFS. ADDomer (1 mg / ml) was labeled with Alexa Flour 488 dye (Invitrogen) following the manufacturer's recommendations. Unbound dye was removed by extensive dialysis against PBS overnight. About 105 monocytes or MDDCs, respectively, were incubated for 1 hour at 37 ° C with 10 μg of labeled ADDomer. Cells were applied to glass coverslips and analyzed using differential interference contrast and green fluorescence channels in an Olympus IX81 inverted microscope.
ADDomer was labeled with Alexa Fluor 680 dye (Invitrogen) following the same procedure as above for Alexa Flour 488 labeling. Alexa Flour 680–labeled ADDomer sample was injected in 9-week-old female BALB/cJRj mice (Janvier Labs, France). Four control mice (no injection) were used for tissue autofluorescence quantifications. Mice were anesthetized (isoflurane/air, 4% for induction and 1.5% thereafter), and injections were performed either subcutaneously (n = 8; right flank; 100 μl; 0.1 mg/ml) or intramuscularly (n = 8; right quadriceps; 12 μl; 0.85 mg/ml). Mice were euthanized at either 1 hour (n = 4 per group) or 5 hours (n = 4 per group) after injection. Main lymph nodes (mesenteric, sciatic, axillary, inguinal, and brachial) were sampled and imaged using FLUOBEAM700 (Fluoptics, France) with 680-nm excitation and LP (Long Pass) 700-nm emission. Fluorescence radiance from each lymph node was quantified in relative light units per pixel per 100 ms.
Initial test immunizations. Six-week-old female BALB/c mice were subcutaneously injected, and sera were collected and treated as described previously (37). Immunizations were carried out with 10 μg each of ADDomer, ADDomer-tevCHIK (uncut), or ADDomer-tevCHIK quantitively cleaved by TEV protease, respectively. Specific antibodies in sera were detected by enzyme-linked immunosorbent assay (ELISA) in duplicate using 96-well plates coated with CHIK peptide (0.1 μg/ml). Horseradish peroxidase (HRP)–conjugated goat anti-mouse IgG 1030-05 (SouthernBiotech) was used for detection [concentration of 0.1 μg/ml in PBS with 1% bovine serum albumin (BSA)] for 1 hour at 37°C, supplemented with 100 μl of tetramethylbenzidine (TMB) substrate (Becton Dickinson) per well. Reactions were stopped by adding H2SO4 (0.2 N), and OD was measured in a microplate reader (Thermo Fisher Scientific) at 450 nm (fig. S7).
ADDomer-tevCHIK immunization experiments. Ten B6D2F1 mice per group received twice (study days 1 and 15) subcutaneously 40 μg per mouse of ADDomer (group 1) or quantitatively cleaved ADDomer-tevCHIK (group 2). Control mice were immunized twice with the buffer diluent. Mice were observed cage-side for clinical symptoms. Mice immunized with ADDomer (group 1) and ADDomer-tevCHIK (group 2) developed high serum IgG titers (<12,800) after the first and second immunization. Mice immunized with diluent did not induce ADDomer-specific IgG. IgM and IgG titers were <100 in serum samples collected before immunization. All mice immunized with ADDomer-tevCHIK sample developed CHIK-specific IgG after the first immunization (GMT, 2425; titer range, 400 to 6400). After the second immunization, IgG titers substantially increased (GMT, 19,400; titer range, 6400 to 51,200). Mice immunized with ADDomer (empty) and diluent did not develop CHIK-specific IgG titers. In contrast, only 1 of 10 mice immunized with ADDomer-tevCHIK developed detectable CHIK epitope–specific IgM after the first (titer, 1:50) and second (titer, 1:100) immunization. No CHIK-specific IgM could be determined in mice immunized with ADDomer or diluent.
Blood was collected by the facial vein technique at days 1, 14, and 35. Briefly, the mouse was gently and securely restrained in the operator’s nondominant hand. The hairless freckle on the side of the jaw was located and pricked with a sharp lancet held by operator’s free hand (sharp end of the lancet points at the far side of the mouse’s face, at the base of the far ear, or at the base of the far side of the mouth). About four to seven drops of blood were collected in an Eppendorf tube, and the mouse was released into its cage. Blood samples were centrifuged twice in a bench centrifuge for 5 min at 10,000g at 4°C, and collected serum was stored below −18°C before analyses. An ELISA protocol was developed using streptavidin-coated plates and the biotinylated CHIK peptide (table S2) following established protocols (Thermo Fisher Scientific). Briefly, streptavidin-coated plates were washed three times with 200 μl of wash buffer [25 mM tris-HCl (pH 7.2), 150 mM NaCl, 0.1% BSA, and 0.05% Tween 20]. Next, 100 μl of biotinylated CHIK peptide dissolved in dimethyl sulfoxide and diluted in PBS to a final concentration of 2.5 μg/ml in PBS was added to each well. Plates were incubated for 2 hours on a plate shaker at room temperature. After extensive washing, twofold serially diluted serum samples were added (100 μl per well). Plates were incubated for 1 hour with occasional shaking at room temperature. After three additional washing steps, 100 μl of goat anti-mouse IgM or HRP-conjugated IgG antibody (diluted 1:2000; Sigma-Aldrich), respectively, was added to each well, and plates were incubated for 45 min at room temperature. Plates were again extensively washed before adding 100 μl of color substrate (TMB) per well, followed by shaking. The color reaction was stopped with H2SO4 (0.2 N), and OD was measured at 450 nm. To determine serum IgM or IgG titers, a cutoff value was defined as mean absorption value of negative blank samples plus three times the SD.
In vivo experimentation statement
In vivo experiments were carried out in France at the Institute for Advanced Biosciences (Grenoble) and the Institute of Biology and Chemistry of Proteins (Lyon). These laboratories are certified by the French Ministry of Research and Education Superior and regularly monitored by the French Departmental Directorate for the Protection of Population (approval numbers C 69 123 0303 and C38 516 10001). Immunization studies were carried out at the Institute of Virology, Biomedical Research Centre, Slovak Academy of Sciences (Bratislava). Animal care was in compliance with the standard operation procedures of the Institute of Virology and the European Convention for the Protection of Vertebrate Animals used for experimental and other scientific purposes (ETS 123) with approval from the Veterinary State Administration, Slovak Republic (Statna veterinarna a potravinova sprava Slovenskej republiky), and institutional ethical committee. All animal experiments were carried out according to the rules in force and in the respect of the ethics of the animal experimentation.
Statistical significance was determined by calculating SDs following standard mathematical formulae (unpaired t test with Welch’s correction of log-transformed titer values).
Supplementary material for this article is available at http://advances.sciencemag.org/cgi/content/full/5/9/eaaw2853/DC1
Fig. S1. ADDomer BioBrick design and expression.
Fig. S2. ADDomer primary sequence.
Fig. S3. EM of ADDomer.
Fig. S4. Quality of the ADDomer map and model.
Fig. S5. ADDomer thermotolerance.
Fig. S6. ADDomer: Genetically encoded multiepitope display.
Fig. S7. Initial immunization experiments.
Fig. S8. Individual specific IgM serum titers.
Fig. S9. ADDomer functionalization.
Table S1. Cryo-EM data collection, refinement, and validation statistics.
Table S2. ADDomer epitope sequences.
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