表位
计算生物学
抗体
计算机科学
生物
化学
免疫学
作者
Guy Nimrod,Sharon Fischman,Mark Austin,Asael Herman,Feenagh Keyes,Olga Leiderman,David Hargreaves,Marek Štrajbl,J. Breed,Shelley Klompus,Kevin Minton,Jennifer Spooner,Andrew Buchanan,Tristan J. Vaughan,Yanay Ofran
出处
期刊:Cell Reports
[Cell Press]
日期:2018-11-01
卷期号:25 (8): 2121-2131.e5
被引量:80
标识
DOI:10.1016/j.celrep.2018.10.081
摘要
The ultimate goal of protein design is to introduce new biological activity. We propose a computational approach for designing functional antibodies by focusing on functional epitopes, integrating large-scale statistical analysis with multiple structural models. Machine learning is used to analyze these models and predict specific residue-residue contacts. We use this approach to design a functional antibody to counter the proinflammatory effect of the cytokine interleukin-17A (IL-17A). X-ray crystallography confirms that the designed antibody binds the targeted epitope and the interaction is mediated by the designed contacts. Cell-based assays confirm that the antibody is functional. Importantly, this approach does not rely on a high-quality 3D model of the designed complex or even a solved structure of the target. As demonstrated here, this approach can be used to design biologically active antibodies, removing some of the main hurdles in antibody design and in drug discovery.
科研通智能强力驱动
Strongly Powered by AbleSci AI