Antibody structure, prediction and redesign

被引:50
作者
Morea, V
Tramontano, A
Rustici, M
Chothia, C
Lesk, AM
机构
[1] IRBM P Angeletti, I-00045 Pomezia, Italy
[2] Univ La Sapienza, Dipartimento Studi Farmaceut, I-00100 Rome, Italy
[3] Univ Sassari, Dipartimento Chim, I-07100 Sassari, Italy
[4] MRC Ctr, Mol Biol Lab, Cambridge CB2 2QH, England
[5] Univ Cambridge, Dept Haematol, Sch Clin, MRC Ctr, Cambridge CB2 2QH, England
基金
英国惠康基金;
关键词
immunoglobulin structure; hypervariable loops; canonical structures; structure prediction; protein design; hair-pin loops;
D O I
10.1016/S0301-4622(96)02266-1
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
So far the difficulty to predict the structure of the third hypervariable loop of the heavy chain of antibodies has represented the main limitation in modelling the complete antigen binding site. We carefully analysed all available structures of immunoglobulins searching for rules relating the loop conformation to its amino acid sequence. Here, we analyse the conformation of this loop and show that we are able to predict the conformation of the ten residues proximal to the framework. The conformation of the remaining residues of loops longer than 10 residues can also be predicted in many cases. This, combined with the previously defined canonical structures for the other five hypervariable loops, is an important step toward the prediction of the complete immunoglobulin antigen-binding site. We exemplify our prediction protocol using three known immunoglobulin structures as test cases. (C) 1997 Elsevier Science B.V.
引用
收藏
页码:9 / 16
页数:8
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