Antibody modeling: Implications for engineering and design

被引:86
作者
Morea, V
Lesk, AM
Tramontano, A
机构
[1] IRBM P Angeletti, I-00040 Rome, Italy
[2] Univ G DAnnunzio, Ist Chim Farm, Chieti, Italy
[3] Univ Cambridge, Sch Clin, Wellcome Trust Ctr Study Mol Mechanisms Dis, Cambridge Inst Med Res, Cambridge CB2 2XY, England
基金
英国惠康基金;
关键词
antibody modeling; canonical structures; CDRs; loop grafting; protein engineering;
D O I
10.1006/meth.1999.0921
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Our understanding of the rules relating sequence to structure in antibodies has led to the development of accurate knowledge-based procedures for antibody modeling. Information gained from the analysis of antibody structures has been successfully exploited to engineer antibody-like molecules endowed with prescribed properties, such as increased stability or different specificity, many of which have a broad spectrum of applications both in therapy and in research. Here we describe a knowledge-based procedure for the prediction of the antibody-variable domains, based on the canonical structures method for the antigen-binding site, and discuss its expected accuracy and limitations. The rational design of antibody-based molecules is illustrated using as an example one of the most widely employed modifications of antibody structures: the humanization of animal-derived antibodies to reduce their immunogenicity for serotherapy in humans. (C) 2000 Academic Press.
引用
收藏
页码:267 / 279
页数:13
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