Germline VH/VL pairing in antibodies

被引:49
作者
Jayaram, Narayan [1 ]
Bhowmick, Pallab [1 ]
Martin, Andrew C. R. [1 ]
机构
[1] UCL, Inst Struct & Mol Biol, Div Biosci, London WC1E 6BT, England
关键词
antibody stability; humanisation; immunoglobulins; immunology; preferred pairing; MURINE MONOCLONAL-ANTIBODIES; RESHAPING HUMAN-ANTIBODIES; VARIABLE DOMAINS; REPERTOIRE; DATABASE; THERAPY; MOUSE; KABAT; MOLECULES; LIBRARIES;
D O I
10.1093/protein/gzs043
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Antibodies are key molecules of the adaptive immune response and are now a major class of biopharmaceuticals. Pairing of heavy and light chains is one of the ways of generating antibody diversity and, while little is known about mechanisms governing V-H/V-L pairing, previous studies have suggested that the germline source from which chains are paired is random. By selecting paired antibody protein sequences from human and mouse antibodies from the KabatMan database and mapping them onto their corresponding germline sequences, we find that pairing preferences do exist in the germline, but only for a small proportion of germline gene segments; others are much more promiscuous showing no preferences. The closest equivalent human and mouse gene families were identified and pairing preferences compared. This work may impact on the ability to generate more stable antibodies for use as biopharmaceuticals.
引用
收藏
页码:523 / 529
页数:7
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