Continuum electrostatic methods applied to pH-dependent properties of antibody-antigen association

被引:17
作者
Gibas, CJ [1 ]
Jambeck, P
Subramaniam, S
机构
[1] Univ Illinois, Natl Ctr Supercomp Applicat, Beckman Inst, Urbana, IL 61801 USA
[2] Univ Illinois, Ctr Biophys & Computat Biol, Urbana, IL 61801 USA
[3] Univ Illinois, Dept Biochem, Urbana, IL 61801 USA
[4] Univ Illinois, Dept Mol & Integrat Physiol, Urbana, IL 61801 USA
关键词
D O I
10.1006/meth.1999.0923
中图分类号
Q5 [生物化学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
Protein association events are a critical component of the functioning of biological systems. Antibody/antigen association, which involves extraordinarily specific interactions, has been a paradigm for the study of structural factors and intermolecular forces controlling protein-protein association. As new experimental approaches to the study of antibody/antigen affinity have become routine, and as more structures of complexes of antibodies and their antigens have become available, it has become possible to use computational approaches to study these interactions. Electrostatic interactions are known to play an important role in protein complex formation. In this review, we focus on the use of continuum electrostatic methods to compute pH-dependent properties of proteins and discuss the use of these methods in the study of antibody/antigen complexes. (C) 2000 Academic Press.
引用
收藏
页码:292 / 309
页数:18
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