OptCDR: a general computational method for the design of antibody complementarity determining regions for targeted epitope binding
Abstract
Antibodies are an important class of proteins with many biomedical and biotechnical applications. Although there are a plethora of experimental techniques geared toward their efficient production, there is a paucity of computational methods for their de novo design. OptCDR is a general computational method to design the binding portions of antibodies to have high specificity and affinity against any targeted epitope of an antigen. First, combinations of canonical structures for the antibody complementarity determining regions (CDRs) that are most likely to be able to favorably bind the antigen are selected. This is followed by the simultaneous refinement of the CDR structures' backbones and optimal amino acid selection for each position. OptCDR is applied to three computational test cases: a peptide from the capsid of hepatitis C, the hapten fluorescein and the protein vascular endothelial growth factor. The results demonstrate that OptCDR can efficiently generate diverse antibody libraries of a pre-specified size with promising antigen affinity potential as exemplified by computationally derived binding metrics.
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Four methods have been made available for computational antibody design: OptCDR, OptMAVEn, AbDesign and RosettaAntibodyDesign.
“Since then, four methods have been made available: OptCDR [139], OptMAVEn[140], AbDesign [143] and RosettaAntibodyDesign [142].”
From Computational approaches to therapeutic antibody design: established methods and emerging trends (2020) · cites this paper as [139]
Cites
Berman, H. M. (2000) · Nucleic Acids Research · doi:10.1093/nar/28.1.235 · Cited by 40,196 · see citing works
The PyMOL Molecular Graphics System
DeLano, W. L. (2002) · Medical Entomology and Zoology · Cited by 18,147 · see citing works
Continuous cultures of fused cells secreting antibody of predefined specificity
Köhler, G., & Milstein, C. (1975) · Nature · doi:10.1038/256495a0 · Cited by 17,200 · see citing works
Naturally occurring antibodies devoid of light chains
Hamers-Casterman, C., Atarhouch, T., Muyldermans, S., Robinson, G., Hammers, C., Songa, E. B., Bendahman, N., & Hammers, R. (1993) · Nature · doi:10.1038/363446a0 · Cited by 3,241 · see citing works
Encyclopedia of Computational Chemistry
(2003) · Wiley eBooks · doi:10.1002/0470845015 · Cited by 2,741 · see citing works
Willett, C. G., Boucher, Y., di Tomaso, E., Duda, D. G., Munn, L. L., Tong, R. T., Chung, D. C., Sahani, D. V., Kalva, S. P., Kozin, S. V., et al. (2004) · Nature Medicine · doi:10.1038/nm988 · Cited by 1,966 · see citing works
Design of a Novel Globular Protein Fold with Atomic-Level Accuracy
Kuhlman, B. A., Dantas, G. A., Ireton, G. C., Varani, G., Stoddard, B. L., & Baker, D. A. (2003) · Science · doi:10.1126/science.1089427 · Cited by 1,666 · see citing works
Canonical structures for the hypervariable regions of immunoglobulins
Chothia, C., & Lesk, A. M. (1987) · Journal of Molecular Biology · doi:10.1016/0022-2836(87)90412-8 · Cited by 1,406 · see citing works
Horder, & Harnett, W. L. (1941) · BMJ · doi:10.1136/bmj.1.4186.493 · Cited by 1,319 · see citing works
Anti-TNFα Therapy of Rheumatoid Arthritis: What Have We Learned?
Feldmann, M., & Maini, R. N. (2001) · Annual Review of Immunology · doi:10.1146/annurev.immunol.19.1.163 · Cited by 1,252 · see citing works
In vitro selection and evolution of functional proteins by using ribosome display
Hanes, J., & Plückthun, A. (1997) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.94.10.4937 · Cited by 1,090 · see citing works
Czerkinsky, C. C., Nilsson, L., Nygren, H., Ouchterlony, Ö., & Tarkowski, A. (1983) · Journal of Immunological Methods · doi:10.1016/0022-1759(83)90308-3 · Cited by 1,056 · see citing works
Directed evolution of antibody fragments with monovalent femtomolar antigen-binding affinity
Boder, E. T., Midelfort, K. S., & Wittrup, K. D. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.170297297 · Cited by 673 · see citing works
Antibody-antigen Interactions: Contact Analysis and Binding Site Topography
MacCallum, R. M., Martin, A. C. R., & Thornton, J. M. (1996) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0548 · Cited by 473 · see citing works
Plosker, G. L., & Figgitt, D. P. (2003) · Drugs · doi:10.2165/00003495-200363080-00005 · Cited by 471 · see citing works
Chen, Y., Wiesmann, C., Fuh, G., Li, B., Christinger, H. W., McKay, P., de Vos, A. M., & Lowman, H. B. (1999) · Journal of Molecular Biology · doi:10.1006/jmbi.1999.3192 · Cited by 447 · see citing works
Computational design of antibody-affinity improvement beyond in vivo maturation
Lippow, S. M., Wittrup, K. D., & Tidor, B. (2007) · Nature Biotechnology · doi:10.1038/nbt1336 · Cited by 342 · see citing works
Collis, A. V. J., Brouwer, A. P., & Martin, A. C. R. (2002) · Journal of Molecular Biology · doi:10.1016/s0022-2836(02)01222-6 · Cited by 256 · see citing works
Enzyme-Linked Immunosorbent Assay (ELISA)
Reen, D. J. (2003) · Humana Press eBooks · doi:10.1385/0-89603-268-x:461 · Cited by 253 · see citing works
Martin, A. C. R., & Thornton, J. M. (1996) · Journal of Molecular Biology · doi:10.1006/jmbi.1996.0617 · Cited by 246 · see citing works
Tailoring in vitro evolution for protein affinity or stability
Jermutus, L., Honegger, A., Schwesinger, F., Hanes, J., & Plückthun, A. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.98.1.75 · Cited by 233 · see citing works
Almagro, J. C., & Fransson, J. (2008) · PubMed · doi:10.2741/2786 · Cited by 222 · see citing works
First-Line Herceptin® Monotherapy in Metastatic Breast Cancer
Vogel, C. L., Cobleigh, M., Tripathy, D., Gutheil, J. C., Harris, L. N., Fehrenbacher, L., Slamon, D. J., Murphy, M., Novotny, W. F., Burchmore, M., et al. (2001) · Oncology · doi:10.1159/000055400 · Cited by 190 · see citing works
Sivasubramanian, A., Sircar, A., Chaudhury, S., & Gray, J. J. (2008) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.22309 · Cited by 185 · see citing works
Clark, L. A., Boriack‐Sjodin, P. A., Eldredge, J. K., Fitch, C., Friedman, B., Hanf, K. J. M., Jarpe, M. B., Liparoto, S. F., Li, Y., Lugovskoy, A. A., et al. (2006) · Protein Science · doi:10.1110/ps.052030506 · Cited by 173 · see citing works
WAM: an improved algorithm for modelling antibodies on the WEB
Whitelegg, N., & Rees, A. R. (2000) · Protein Engineering Design and Selection · doi:10.1093/protein/13.12.819 · Cited by 159 · see citing works
A general method for greatly improving the affinity of antibodies by using combinatorial libraries
Rajpal, A., Beyaz, N., Haber, L., Cappuccilli, G., Yee, H., Bhatt, R. R., Takeuchi, T., Lerner, R. A., & Crea, R. (2005) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0503543102 · Cited by 155 · see citing works
Library analysis of SCHEMA‐guided protein recombination
Meyer, M. M., Silberg, J. J., Voigt, C. A., Endelman, J. B., Mayo, S. L., Wang, Z., & Arnold, F. H. (2003) · Protein Science · doi:10.1110/ps.0306603 · Cited by 150 · see citing works
Affinity maturation of antibodies assisted by in silico modeling
Barderas, R., Desmet, J., Timmerman, P., Meloen, R. H., & Casal, J. I. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0801221105 · Cited by 142 · see citing works
Preliminary results of early clinical trials with the fully human anti-TNFα monoclonal antibody D2E7
Kempeni, J. (1999) · Annals of the Rheumatic Diseases · doi:10.1136/ard.58.2008.i70 · Cited by 131 · see citing works
Antibody Modeling: Implications for Engineering and Design
Morea, V., Lesk, A. M., & Tramontano, A. L. (2000) · Methods · doi:10.1006/meth.1999.0921 · Cited by 123 · see citing works
Prediction of loop geometries using a generalized born model of solvation effects
Rapp, C. S., & Friesner, R. A. (1999) · Proteins Structure Function and Bioinformatics · doi:10.1002/(sici)1097-0134(19990501)35:2 · Cited by 103 · see citing works
De Novo Design of a Single-Chain Diphenylporphyrin Metalloprotein
Bender, G. M., Lehmann, A., Zou, H., Cheng, H., Fry, H. C., Engel, D., Therien, M. J., Blasie, J. K., Röder, H., Saven, J. G., et al. (2007) · Journal of the American Chemical Society · doi:10.1021/ja071199j · Cited by 97 · see citing works
Computational design of Candida boidinii xylose reductase for altered cofactor specificity
Khoury, G. A., Fazelinia, H., Chin, J. W., Pantazes, R. J., Cirino, P. C., & Maranas, C. D. (2009) · Protein Science · doi:10.1002/pro.227 · Cited by 91 · see citing works
Self-citationIn vitro evolution of single-chain antibodies using mRNA display
Fukuda, I., Kojoh, K., Tabata, N., Doi, N., Takashima, H., Miyamoto‐Sato, E., & Yanagawa, H. (2006) · Nucleic Acids Research · doi:10.1093/nar/gkl618 · Cited by 90 · see citing works
1.85 Å structure of anti-fluorescein 4-4-20 Fab
Whitlow, M. D., Howard, A. J., Wood, J. F., Voss, E. W., & Hardman, K. D. (1995) · Protein Engineering Design and Selection · doi:10.1093/protein/8.8.749 · Cited by 75 · see citing works
FamClash: A method for ranking the activity of engineered enzymes
Saraf, M. C., Horswill, A. R., Benkovic, S. J., & Maranas, C. D. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0400065101 · Cited by 74 · see citing works
Self-citationA Focused Antibody Library for Improved Hapten Recognition
Persson, H., Lantto, J., & Ohlin, M. (2006) · Journal of Molecular Biology · doi:10.1016/j.jmb.2006.01.004 · Cited by 72 · see citing works
Offredi, F., Dubail, F., Kischel, P., Sarinski, K., Stern, A., de Weerdt, C. V., Hoch, J. C., Prosperi-Meys, C., François, J. M., Mayo, S. L., et al. (2002) · Journal of Molecular Biology · doi:10.1016/s0022-2836(02)01206-8 · Cited by 71 · see citing works
Efficient Recovery of High-Affinity Antibodies from a Single-Chain Fab Yeast Display Library
Walker, L. M., Bowley, D. R., & Burton, D. R. (2009) · Journal of Molecular Biology · doi:10.1016/j.jmb.2009.04.019 · Cited by 67 · see citing works
IPRO: An Iterative Computational Protein Library Redesign and Optimization Procedure
Saraf, M. C., Moore, G. L., Goodey, N. M., Cao, V. Y., Benkovic, S. J., & Maranas, C. D. (2006) · Biophysical Journal · doi:10.1529/biophysj.105.079277 · Cited by 63 · see citing works
Self-citationA de novo redesign of the WW domain
Kraemer-Chant, C. M., Lecomte, J. T. J., & Desjarlais, J. R. (2003) · Protein Science · doi:10.1110/ps.03190903 · Cited by 61 · see citing works
Tailoring in vitro evolution for protein affinity or stability
Jermutus, L. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.011311398 · Cited by 57 · see citing works
Covalent antibody display--an in vitro antibody-DNA library selection system
Reiersen, H. (2005) · Nucleic Acids Research · doi:10.1093/nar/gni010 · Cited by 55 · see citing works
Pantazes, R. J., Saraf, M. C., & Maranas, C. D. (2007) · Protein Engineering Design and Selection · doi:10.1093/protein/gzm030 · Cited by 41 · see citing works
Self-citationFazelinia, H., Cirino, P. C., & Maranas, C. D. (2008) · Protein Science · doi:10.1002/pro.2 · Cited by 40 · see citing works
Self-citationFazelinia, H., Cirino, P. C., & Maranas, C. D. (2007) · Biophysical Journal · doi:10.1529/biophysj.106.096016 · Cited by 29 · see citing works
Self-citationMénez, R., Bossus, M., Muller, B. H., Sibaı̈, G., Dalbon, P., Ducancel, F., Jolivet‐Reynaud, C., & Stura, E. A. (2003) · The Journal of Immunology · doi:10.4049/jimmunol.170.4.1917 · Cited by 27 · see citing works
Pascalis, R. D., Gonzales, N. R., PADLAN, E. A., Schuck, P., Batra, S. K., Schlom, J., & Kashmiri, S. V. S. (2003) · PubMed · Cited by 24 · see citing works
An antibody loop replacement design feasibility study and a loop-swapped dimer structure
Clark, L. A., Boriack‐Sjodin, P. A., Day, E. S., Eldredge, J. K., Fitch, C., Jarpe, M. B., Miller, S., Li, Y., Simon, K. J., & van Vlijmen, H. (2008) · Protein Engineering Design and Selection · doi:10.1093/protein/gzn072 · Cited by 14 · see citing works
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Sorted by citations
Macromolecular modeling and design in Rosetta: recent methods and frameworks
Leman, J. K., Weitzner, B. D., Lewis, S. M., Adolf-Bryfogle, J., Alam, N., Alford, R. F., Aprahamian, M., Baker, D., Barlow, K. A., Barth, P., et al. (2020) · Nature Methods · doi:10.1038/s41592-020-0848-2 · Cited by 888 · see citing works
Tiller, K. E., & Tessier, P. M. (2015) · Annual Review of Biomedical Engineering · doi:10.1146/annurev-bioeng-071114-040733 · Cited by 255 · see citing works
RosettaAntibodyDesign (RAbD): a general framework for computational antibody design
Adolf-Bryfogle, J., Kalyuzhniy, O., Kubitz, M., Weitzner, B. D., Hu, X., Adachi, Y., Schief, W. R., & Dunbrack, R. L. (2018) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006112 · Cited by 227 · see citing works
Computational approaches to therapeutic antibody design: established methods and emerging trends
Norman, R. A., Ambrosetti, F., Bonvin, A. M. J. J., Colwell, L. J., Kelm, S., Kumar, S., & Krawczyk, K. (2020) · Briefings in Bioinformatics · doi:10.1093/bib/bbz095 · Cited by 219 · see citing works
“Since then, four methods have been made available: OptCDR [139], OptMAVEn[140], AbDesign [143] and RosettaAntibodyDesign [142].”
MethodProtein folding and de novo protein design for biotechnological applications
Khoury, G. A., Smadbeck, J. B., Kieslich, C. A., & Floudas, C. A. (2013) · Trends in biotechnology · doi:10.1016/j.tibtech.2013.10.008 · Cited by 162 · see citing works
Luo, S., Su, Y., Peng, X., Wang, S., Peng, J., & Ma, J. (2022) · doi:10.1101/2022.07.10.499510 · Cited by 151 · see citing works
Luo, S., Su, Y., Peng, J., Wang, S., Peng, J., & Ma, J. (2022) · neural information processing systems · doi:10.52202/068431-0709 · Cited by 149 · see citing works
Rational design of antibodies targeting specific epitopes within intrinsically disordered proteins
Sormanni, P., Aprile, F. A., & Vendruscolo, M. (2015) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1422401112 · Cited by 145 · see citing works
Third generation antibody discovery methods: in silico rational design
Sormanni, P., Aprile, F. A., & Vendruscolo, M. (2018) · Chemical Society Reviews · doi:10.1039/c8cs00523k · Cited by 136 · see citing works
Lapidoth, G. D., Baran, D., Pszolla, G. M., Norn, C., Alon, A., Tyka, M. D., & Fleishman, S. J. (2015) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.24779 · Cited by 107 · see citing works
Khoury, G. A., Thompson, J. P., Smadbeck, J. B., Kieslich, C. A., & Floudas, C. A. (2013) · Journal of Chemical Theory and Computation · doi:10.1021/ct400556v · Cited by 104 · see citing works
Li, L., Gupta, E., Spaeth, J., Shing, L., Jaimes, R., Engelhart, E., Lopez, R., Caceres, R. S., Bepler, T., & Walsh, M. E. (2023) · Nature Communications · doi:10.1038/s41467-023-39022-2 · Cited by 96 · see citing works
Analysis and modeling of the variable region of camelid single-domain antibodies
Sircar, A., Sanni, K. A., Shi, J., & Gray, J. J. (2011) · The Journal of Immunology · doi:10.4049/jimmunol.1100116 · Cited by 92 · see citing works
Recent advances in computational protein design
Pantazes, R. J., Grisewood, M. J., & Maranas, C. D. (2011) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2011.04.005 · Cited by 87 · see citing works
Self-citationsdAb-DB: the single domain antibody database
Wilton, E. E., Opyr, M. P., Kailasam, S., Kothe, R. F., & Wieden, H.-J. (2018) · ACS Synthetic Biology · doi:10.1021/acssynbio.8b00407 · Cited by 84 · see citing works
Li, T., Pantazes, R. J., & Maranas, C. D. (2014) · PLoS ONE · doi:10.1371/journal.pone.0105954 · Cited by 79 · see citing works
Self-citationComparative Analysis of the CDR Loops of Antigen Receptors
Wong, W. K., Leem, J., & Deane, C. M. (2019) · Frontiers in Immunology · doi:10.3389/fimmu.2019.02454 · Cited by 75 · see citing works
T-Cell Engagers in Solid Cancers—Current Landscape and Future Directions
Shanshal, M., Caimi, P. F., Adjei, A. A., & Ma, W. W. (2023) · Cancers · doi:10.3390/cancers15102824 · Cited by 73 · see citing works
Iterative Refinement Graph Neural Network for Antibody Sequence-Structure Co-designPreprint
Jin, W., Wohlwend, J., Barzilay, R., & Jaakkola, T. (2021) · arXiv (Cornell University) · doi:10.48550/arxiv.2110.04624 · Cited by 85 · see citing works
Structure-Based, Rational Design of T Cell Receptors
Zoete, V., Irving, M. B., Ferber, M., Cuendet, M. A., & Michielin, O. A. (2013) · Frontiers in Immunology · doi:10.3389/fimmu.2013.00268 · Cited by 62 · see citing works
Computational design of antibodies
Fischman, S., & Ofran, Y. (2018) · Current Opinion in Structural Biology · doi:10.1016/j.sbi.2018.04.007 · Cited by 56 · see citing works
Bai, G., Sun, C., Guo, Z., Wang, Y., Zeng, X., Su, Y., Zhao, Q., & Ma, B. (2023) · Seminars in Cancer Biology · doi:10.1016/j.semcancer.2023.06.005 · Cited by 56 · see citing works
Dewaker, V., Morya, V. K., Kim, Y. H., Park, S. T., Kim, H. S., & Koh, Y. H. (2025) · Biomarker Research · doi:10.1186/s40364-025-00764-4 · Cited by 59 · see citing works
Length-independent structural similarities enrich the antibody CDR canonical class model
Nowak, J., BAKER, T. S., Georges, G. J., Kelm, S., Klostermann, S., Shi, J., Sridharan, S., & Deane, C. M. (2016) · mAbs · doi:10.1080/19420862.2016.1158370 · Cited by 54 · see citing works
OptMAVEn-2.0: De novo Design of Variable Antibody Regions against Targeted Antigen Epitopes
Chowdhury, R., Allan, M. F., & Maranas, C. D. (2018) · Antibodies · doi:10.3390/antib7030023 · Cited by 55 · see citing works
Self-citationmmCSM-AB: guiding rational antibody engineering through multiple point mutations
Myung, Y., Pires, D. E. V., & Ascher, D. B. (2020) · Nucleic Acids Research · doi:10.1093/nar/gkaa389 · Cited by 51 · see citing works
Yu, C.-M., Peng, H., Chen, I.-C., Lee, Y., Chen, J.-B., Tsai, K., Chen, C.-T., Chang, J.-Y., Yang, E.-W., Hsu, P., et al. (2012) · PLoS ONE · doi:10.1371/journal.pone.0033340 · Cited by 48 · see citing works
Abskharon, R. N. N., Pan, H., Sawaya, M. R., Seidler, P. M., Olivares, E. J., Chen, Y., Murray, K. A., Zhang, J., Lantz, C., Bentzel, M., et al. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2300258120 · Cited by 47 · see citing works
Polonsky, K., Pupko, T., & Freund, N. T. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2300150 · Cited by 41 · see citing works
The Iterative Protein Redesign and Optimization (IPRO) suite of programs
Pantazes, R. J., Grisewood, M. J., Li, T., Gifford, N. P., & Maranas, C. D. (2014) · Journal of Computational Chemistry · doi:10.1002/jcc.23796 · Cited by 40 · see citing works
Self-citationApplications of Machine and Deep Learning in Adaptive Immunity
Pertseva, M., Gao, B., Neumeier, D., Yermanos, A., & Reddy, S. T. (2021) · Annual Review of Chemical and Biomolecular Engineering · doi:10.1146/annurev-chembioeng-101420-125021 · Cited by 38 · see citing works
De Novo Design and Experimental Characterization of Ultrashort Self-Associating Peptides
Smadbeck, J. B., Chan, K. H., Khoury, G. A., Xue, B., Robinson, R. C., Hauser, C. A. E., & Floudas, C. A. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003718 · Cited by 37 · see citing works
Computational de novo design of antibodies binding to a peptide with high affinity
Poosarla, V. G., Li, T., Goh, B. C., Schulten, K. J., Wood, T. K., & Maranas, C. D. (2017) · Biotechnology and Bioengineering · doi:10.1002/bit.26244 · Cited by 35 · see citing works
Self-citationDe novo design of antibody complementarity determining regions binding a FLAG tetra-peptide
Entzminger, K. C., Hyun, J., Pantazes, R. J., Patterson-Orazem, A. C., Qerqez, A. N., Frye, Z., Hughes, R. A., Ellington, A. D., Lieberman, R. L., Maranas, C. D., et al. (2017) · Scientific Reports · doi:10.1038/s41598-017-10737-9 · Cited by 35 · see citing works
Self-citationYang, Y. X., Wang, P., & Zhu, B. T. (2022) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2022.108364 · Cited by 30 · see citing works
Zhang, F., Liu, B., Liu, G., Zhang, Y., Wang, J., & Wang, S. (2018) · Scientific Reports · doi:10.1038/s41598-018-21394-x · Cited by 30 · see citing works
Computational tools for aiding rational antibody design
Krawczyk, K., Dunbar, J., & Deane, C. M. (2017) · Methods in molecular biology · doi:10.1007/978-1-4939-6637-0_21 · Cited by 26 · see citing works
How can we discover developable antibody-based biotherapeutics?
Bauer, J., Rajagopal, N., Gupta, P., Gupta, P. K., Nixon, A. E., & Kumar, S. (2023) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2023.1221626 · Cited by 27 · see citing works
IgGM: A Generative Model for Functional Antibody and Nanobody DesignPreprint
Wang, R., Wu, F., Gao, X., Wu, J., Zhao, P., & Yao, J. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.09.19.613838 · Cited by 26 · see citing works
AI-driven innovation in antibody-drug conjugate design
Noriega, H. A., & Wang, X. S. (2025) · Frontiers in Drug Discovery · doi:10.3389/fddsv.2025.1628789 · Cited by 25 · see citing works
Pantazes, R. J., & Maranas, C. D. (2013) · BMC Bioinformatics · doi:10.1186/1471-2105-14-168 · Cited by 24 · see citing works
Self-citationAntibody side chain conformations are position-dependent
Leem, J., Georges, G., Shi, J., & Deane, C. M. (2018) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.25453 · Cited by 22 · see citing works
Neamțu, A., Mocci, F., Laaksonen, A., & da Silva, F. L. B. (2022) · Colloids and Surfaces B Biointerfaces · doi:10.1016/j.colsurfb.2022.112986 · Cited by 22 · see citing works
Structure-based non-canonical amino acid design to covalently crosslink an antibody–antigen complex
Xu, J., Tack, D. S., Hughes, R. A., Ellington, A. D., & Gray, J. J. (2013) · Journal of Structural Biology · doi:10.1016/j.jsb.2013.05.003 · Cited by 22 · see citing works
Antibodies: Computer-Aided Prediction of Structure and Design of Function
Sevy, A. M., & Meiler, J. (2014) · Microbiology Spectrum · doi:10.1128/microbiolspec.aid-0024-2014 · Cited by 21 · see citing works
An outlook on structural biology after A lpha F old: tools, limits and perspectives
Rosignoli, S., Pacelli, M., Manganiello, F., & Paiardini, A. (2024) · FEBS Open Bio · doi:10.1002/2211-5463.13902 · Cited by 18 · see citing works
Cuevas, S. A. P., Etchebest, C., & da Silva, F. L. B. (2019) · Journal of Chemical Information and Modeling · doi:10.1021/acs.jcim.9b00895 · Cited by 17 · see citing works
Bielska, W., Jaszczyszyn, I., Dudzic, P., Janusz, B., Chomicz, D., Wrobel, S., Greiff, V., Feehan, R., Adolf‐Bryfogle, J., & Krawczyk, K. (2025) · Frontiers in Immunology · doi:10.3389/fimmu.2025.1571371 · Cited by 16 · see citing works
Lauro, A. D., Rienzo, L. D., Miotto, M., Olimpieri, P. P., Milanetti, E., & Ruocco, G. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.874296 · Cited by 15 · see citing works
Qiao, C., Lv, M., Li, X., Geng, J., Li, Y., Zhang, J., Zhou, L., Feng, J., & Shen, B. (2012) · Journal of Biomolecular Structure and Dynamics · doi:10.1080/07391102.2012.706073 · Cited by 14 · see citing works
Improved HIV-1 neutralization breadth and potency of V2-apex antibodies by in silico design
Holt, G. T., Gorman, J., Wang, S., Lowegard, A. U., Zhang, B., Liu, T. W. B., Lin, B. C., Louder, M. K., Frenkel, M. S., McKee, K., et al. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112711 · Cited by 13 · see citing works
Gallo, E. (2024) · Molecular Biotechnology · doi:10.1007/s12033-024-01064-2 · Cited by 16 · see citing works
Structural and Functional Properties of Proteins
Poluri, K. M., Gulati, K., & Sarkar, S. (2021) · Springer eBooks · doi:10.1007/978-981-16-1594-8_1 · Cited by 13 · see citing works
Predicting phenotype transition probabilities via conditional algorithmic probability approximations
Dingle, K., Novev, J. K., Ahnert, S. E., & Louis, A. A. (2022) · Journal of the Royal Society Interface · doi:10.1098/rsif.2022.0694 · Cited by 13 · see citing works
Understanding and Modulating Antibody Fine Specificity: Lessons from Combinatorial Biology
Rojas, G. (2022) · Antibodies · doi:10.3390/antib11030048 · Cited by 11 · see citing works
In Silico Engineering Towards Enhancement of Bap–VHH Monoclonal Antibody Binding Affinity
Sefid, F., Payandeh, Z., Azamirad, G., Abdolhamidi, R., & Rasooli, I. (2018) · International Journal of Peptide Research and Therapeutics · doi:10.1007/s10989-017-9670-9 · Cited by 12 · see citing works
FlowDesign: Improved design of antibody CDRs through flow matching and better prior distributions
Wu, J., Kong, X., Sun, N., Wei, J., Shan, S., Feng, F., Wu, F., Peng, J., Zhang, L., Liu, Y., et al. (2025) · Cell Systems · doi:10.1016/j.cels.2025.101270 · Cited by 11 · see citing works
RosettaAntibodyDesign (RAbD): A General Framework for Computational Antibody DesignPreprint
Adolf-Bryfogle, J., Kalyuzhniy, O., Kubitz, M., Weitzner, B. D., Hu, X., Adachi, Y., Schief, W. R., & Dunbrack, R. L. (2017) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/183350 · Cited by 11 · see citing works
Challenges in Detection of Serum Oncoprotein: Relevance to Breast Cancer Diagnostics
Lengfeld, J. E., Zhang, H., Stoesz, S. P., Murali, R., Pass, F., Greene, M. I., Goel, P. N., & Grover, P. (2021) · Breast Cancer Targets and Therapy · doi:10.2147/bctt.s331844 · Cited by 10 · see citing works
A comprehensive structural model for the human KCNQ1/KCNE1 ion channel
Hasani, H. J., Ahmed, M., & Barakat, K. (2017) · Journal of Molecular Graphics and Modelling · doi:10.1016/j.jmgm.2017.09.019 · Cited by 10 · see citing works
Lee, D. C. P., Raman, R., Ghafar, N. A., & Budigi, Y. (2021) · Antiviral Research · doi:10.1016/j.antiviral.2021.105105 · Cited by 8 · see citing works
Prediction of Paratope–Epitope Pairs Using Convolutional Neural Networks
Li, D., Pucci, F., & Rooman, M. J. (2024) · International Journal of Molecular Sciences · doi:10.3390/ijms25105434 · Cited by 10 · see citing works
MutDock: A computational docking approach for fixed-backbone protein scaffold design
Chauhan, V. M., & Pantazes, R. J. (2022) · Frontiers in Molecular Biosciences · doi:10.3389/fmolb.2022.933400 · Cited by 8 · see citing works
Self-citationNanodesigner: resolving the complex-CDR interdependency with iterative refinement
Zertuche, M. M. R., Kafkas, Ş., Renn, D., Rueping, M., & Hoehndorf, R. (2025) · Journal of Cheminformatics · doi:10.1186/s13321-025-01069-2 · Cited by 6 · see citing works
Corbeil, C. R., Manenda, M. S., Sulea, T. I., Baardsnes, J., Picard, M.-È., Hogues, H., Gaudreault, F., Deprez, C., Shi, R., & Purisima, E. O. (2021) · Scientific Reports · doi:10.1038/s41598-021-00669-w · Cited by 6 · see citing works
Antibody Complementarity Determining Regions (CDRs) design using Constrained Energy Model
Fu, T., & Sun, J. (2022) · ACM SIGKDD Conference on Knowledge Discovery and Data Mining (KDD) · doi:10.1145/3534678.3539285 · Cited by 6 · see citing works
Leong, S. W., Lim, T. S., Ismail, A., & Choong, Y. S. (2017) · Journal of Molecular Recognition · doi:10.1002/jmr.2695 · Cited by 6 · see citing works
Richard, A. C., & Pantazes, R. J. (2024) · Proteins Structure Function and Bioinformatics · doi:10.1002/prot.26773 · Cited by 6 · see citing works
Self-citationProgress toward new function and design of extracellular G protein-coupled receptor nanobodies
Schlimgen, R. R., & Volkman, B. F. (2025) · Molecular Pharmacology · doi:10.1016/j.molpha.2025.100054 · Cited by 5 · see citing works
Protein Engineering Methods to Design Protein Therapeutics
Narad, P., Gupta, R., Gupta, I., & Sengupta, A. (2023) · Springer eBooks · doi:10.1007/978-981-19-8249-1_3 · Cited by 5 · see citing works
Sumner, C. A., Schwedler, J. L., McCoy, K. M., Holland, J., Duva, V., Gelperin, D. M., Busygina, V., Stefan, M. A., Martinez, D. V., Juarros, M. A., et al. (2025) · Protein Science · doi:10.1002/pro.70043 · Cited by 3 · see citing works
Antibodies: Computer-Aided Prediction of Structure and Design of Function
Sevy, A. M., & Meiler, J. (2015) · ASM Press eBooks · doi:10.1128/9781555817411.ch10 · Cited by 4 · see citing works
Biotechnological and Biomedical Applications of Protein Engineering Methods
Poluri, K. M., & Gulati, K. (2016) · SpringerBriefs in applied sciences and technology · doi:10.1007/978-981-10-2732-1_5 · Cited by 4 · see citing works
Conformational stability of the tetrameric de novo designed hexcoil-Ala helical bundle
Demır, K., Alıcı, H., & Yaşar, F. (2017) · Chinese Journal of Physics · doi:10.1016/j.cjph.2017.12.004 · Cited by 4 · see citing works
Yadav, A. J., Bhagat, K., Sharma, A., & Padhi, A. K. (2025) · Advances in protein chemistry and structural biology · doi:10.1016/bs.apcsb.2024.10.011 · Cited by 3 · see citing works
Wang, Z., Li, X.-G., Xie, Y., Wen, Z., Jin, R., Takada, H., & Nagatomi, R. (2024) · IEEE Access · doi:10.1109/access.2024.3416461 · Cited by 3 · see citing works
Austin, K., Torres, J. A., Waters, J. D. V., Balog, E. R. M., Halpern, J. M., & Pantazes, R. J. (2024) · ACS Omega · doi:10.1021/acsomega.4c06481 · Cited by 2 · see citing works
Self-citationRecktenwald, M., Bhattacharya, R., Benmassaoud, M. M., MacAulay, J., Chauhan, V. M., Davis, L., Hutt, E., Galie, P. A., Staehle, M. M., Daringer, N. M., et al. (2024) · ACS Synthetic Biology · doi:10.1021/acssynbio.4c00482 · Cited by 2 · see citing works
Self-citationArtificial intelligence advancements in monoclonal antibody development technology
Ammar, M., Samsonov, M. Y., Gurylina, E., & Bayzigitov, D. R. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1802038 · Cited by 1 · see citing works
Bioinformatics Resources, Tools, and Strategies in Designing Therapeutic Proteins
Sudhan, M., Roshni, J., Janakiraman, V., Sivakumar, M., & Ahmed, S. F. (2022) · Springer eBooks · doi:10.1007/978-981-16-7897-4_7 · Cited by 1 · see citing works
Molecular Engineering of Enzymes
Ortiz‐Soto, M. E., & Seibel, J. (2017) · doi:10.1002/9783527800599.ch3 · Cited by 1 · see citing works
Co-evolution integrated deep learning framework for variants generation and fitness predictionPreprint
Tan, X. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.28.526023 · Cited by 1 · see citing works
Antibody Modeling, Engineering, and Design
Fischman, S., & Ofran, Y. (2018) · Springer eBooks · doi:10.1007/978-3-642-35943-9_10083-1
Jamialahmadi, B., Chamankhah, M., Kohandel, M., & Ghodsi, A. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.07.16.603820
DiffNB: Aligning a Nanobody Diffusion Model with Direct Preference Optimization
Wu, Y., JiaShu, Wu, D., Qin, Y., Plötz, T., Hrovatin, K., Linker, S. M., Hopp, A. V., Winkel, M., Harbach, P. H. P., et al. (2025) · IEEE International Conference on Bioinformatics and Biomedicine (BIBM) · doi:10.1109/bibm66473.2025.11356690
RankNB: Ranking-Aware Direct Preference Optimization for Alignment of a Nanobody Diffusion Model
Wu, Y., Wu, D., Shu, J., Linker, S. M., Hrovatin, K., Winkel, M., & Tan, F. (2026) · IEEE International Conference on Acoustics Speech and Signal Processing · doi:10.1109/icassp55912.2026.11462703
Antibody Affinity Maturation by Computational Design
Abualrous, E. T., Miller, W., & Cannon, D. A. (2026) · Methods in molecular biology · doi:10.1007/978-1-0716-5041-7_4
AI-Driven Design Platforms of Next-Generation Antibody Therapeutics
Wang, Y., Saba, A., Ran, Y., Shehzadi, K., Zhang, Q., Jianhua, L., & Yu, M. (2026) · Topics in Current Chemistry · doi:10.1007/s41061-026-00554-y
Luo, G., Wang, J., Zhang, S., Zhu, Z., Lu, Z., & Li, M. (2026) · Bioinformatics · doi:10.1093/bioinformatics/btag606
Shi, Z., Xu, X., Zhang, H., Ren, S., & Wang, H. (2026) · Swarm and Evolutionary Computation · doi:10.1016/j.swevo.2026.102526
Biotechnological applications of engineered proteins: advancements and challenges
Pusala, B., Sharma, B., Agarwal, S., Gulati, K., & Poluri, K. M. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-44536-1.00015-8
Machine learning and artificial intelligence in protein design
Madala, B. P., & Kumar, R. (2026) · Elsevier eBooks · doi:10.1016/b978-0-443-44536-1.00013-4
Relation-Aware Graph–Hypergraph Networks for Antibody Sequence–Structure Co-DesignPreprint
Wei, J., Zhang, S., Duan, H., Wei, L., & GUO, J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.10.12.758263
- Authors
- Pantazes, R. J., & Maranas, C. D.
- Affiliations
- Pennsylvania State University (US)
- Venue
- Protein Engineering Design and Selection
- Publisher
- Oxford University Press (OUP)
- Published
- 2010-09-16
- Volume
- 23
- Issue
- 11
- Pages
- 849-858
- ISSN
- 0269-2139 (ISSN-L)
- 1741-0126
- 1741-0134
- OpenAlex
- W2160415526
- Cited by
- 97
- References
- 50
- Citations by year
- 2026: 9 · 2025: 9 · 2024: 9 · 2023: 9 · 2022: 9 · 2021: 8 · 2020: 2 · 2019: 4 · 2018: 10 · 2017: 7 · 2016: 3 · 2015: 4 · 2014: 4 · 2013: 6 · 2012: 2
- FWCI
- 1.30
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Protein Engineering Design and Selection (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protein Structure and Dynamics
- Health Sciences › Medicine › Radiology, Nuclear Medicine and Imaging › Monoclonal and Polyclonal Antibodies Research
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › vaccines and immunoinformatics approaches
- Keywords
- de novo antibody design, epitope binding, amino acid selection, antibody libraries, fluorescein, vascular endothelial growth factor, binding affinity prediction
- MeSH terms
- Amino Acid Sequence, Antibodies, Antibody Affinity, Epitopes, Capsid, Computer Simulation, Haptens, Models, Molecular, Molecular Sequence Data, Viral Proteins, Hepacivirus, Models, Immunological, Fluorescein, Complementarity Determining Regions, Vascular Endothelial Growth Factor A
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