The Allostery Landscape: Quantifying Thermodynamic Couplings in Biomolecular Systems

被引:24
作者
Cuendet, Michel A. [1 ,2 ,3 ]
Weinstein, Harel [1 ,2 ]
LeVine, Michael V. [1 ,2 ]
机构
[1] Cornell Univ, Weill Cornell Med Coll, Dept Physiol & Biophys, New York, NY 10065 USA
[2] Cornell Univ, Weill Cornell Med Coll, HRH Prince Alwaleed Bin Talal Bin Abdulaziz Alsau, New York, NY 10065 USA
[3] UNIL Sorge, Swiss Inst Bioinformat, CH-1015 Lausanne, Switzerland
基金
美国国家卫生研究院;
关键词
FREE-ENERGY DYNAMICS; BETA(2)-ADRENERGIC RECEPTOR; FUNCTIONAL SELECTIVITY; ADIABATIC DYNAMICS; FORCE-FIELDS; SIMULATIONS; CONFORMATIONS; INFORMATION; PROTEINS; DISTRIBUTIONS;
D O I
10.1021/acs.jctc.6b00841
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Allostery plays a fundamental role in most biological processes. However, little theory is available to describe it outside of two-state models. Here we use a statistical mechanical approach to show that the allosteric coupling between two collective variables is not a single number, but instead a two-dimensional thermodynamic coupling function that is directly related to the mutual information from information theory and the copula density function from probability theory. On this basis, we demonstrate how to quantify the contribution of specific energy terms to this thermodynamic coupling function, enabling an approximate decomposition that reveals the mechanism of allostery. We illustrate the thermodynamic coupling function and its use by showing how allosteric coupling in the alanine dipeptide molecule contributes to the overall shape of the Phi/Psi free energy surface, and by identifying the interactions that are necessary for this coupling.
引用
收藏
页码:5758 / 5767
页数:10
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