| Literature DB >> 31626279 |
Richard A Norman1, Francesco Ambrosetti2,3, Alexandre M J J Bonvin3, Lucy J Colwell4, Sebastian Kelm5, Sandeep Kumar6, Konrad Krawczyk7.
Abstract
Antibodies are proteins that recognize the molecular surfaces of potentially noxious molecules to mount an adaptive immune response or, in the case of autoimmune diseases, molecules that are part of healthy cells and tissues. Due to their binding versatility, antibodies are currently the largest class of biotherapeutics, with five monoclonal antibodies ranked in the top 10 blockbuster drugs. Computational advances in protein modelling and design can have a tangible impact on antibody-based therapeutic development. Antibody-specific computational protocols currently benefit from an increasing volume of data provided by next generation sequencing and application to related drug modalities based on traditional antibodies, such as nanobodies. Here we present a structured overview of available databases, methods and emerging trends in computational antibody analysis and contextualize them towards the engineering of candidate antibody therapeutics.Entities:
Keywords: antibody–antigen complexes; databases; docking; homology modelling; therapeutic antibodies
Year: 2020 PMID: 31626279 PMCID: PMC7947987 DOI: 10.1093/bib/bbz095
Source DB: PubMed Journal: Brief Bioinform ISSN: 1467-5463 Impact factor: 11.622