The diversity of physical forces and mechanisms in intermolecular interactions

被引:41
作者
Berezovsky, Igor N. [1 ]
机构
[1] Univ Bergen, Bergen Ctr Computat Sci, Computat Biol Unit, N-5008 Bergen, Norway
来源
PHYSICAL BIOLOGY | 2011年 / 8卷 / 03期
关键词
AGGREGATION RATES; PROTEIN COMPLEXES; PRINCIPLES; THERMODYNAMICS; PROPENSITIES; PREDICTION; SEQUENCES; PEPTIDE; CHAINS;
D O I
10.1088/1478-3975/8/3/035002
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
Intermolecular interactions became an inherent part of the structure-function paradigm. Therefore, the generalized concept of protein stability and interactions should consider the balance of stabilizing forces working in different types of intermolecular interactions. We consider here two 'extremes' of protein interactions, viral protein with high intrinsic disorder and hyperthermostable protein complexes. Intermolecular interactions provide folding upon binding as a part of function in the viral case, while they secure and stabilize specific native interfaces as a prerequisite for function in hyperthermostable complexes. We propose a generalized concept of protein stability and interactions, which includes intermolecular interactions comprising distinct combinations of stabilizing forces depending on the types of interacting partners.
引用
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页数:11
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