Normal Mode Analysis of Biomolecular Structures: Functional Mechanisms of Membrane Proteins

被引:430
作者
Bahar, Ivet [1 ]
Lezon, Timothy R. [1 ]
Bakan, Ahmet [1 ]
Shrivastava, Indira H. [1 ]
机构
[1] Univ Pittsburgh, Sch Med, Dept Computat Biol, Pittsburgh, PA 15213 USA
关键词
MOLECULAR-DYNAMICS SIMULATIONS; NICOTINIC ACETYLCHOLINE-RECEPTOR; FREQUENCY NORMAL-MODES; ELASTIC NETWORK MODEL; LIGHT-DEPENDENT CHANGES; LIGAND-BINDING DOMAIN; COARSE-GRAINED MODEL; IDENTIFYING CONFORMATIONAL-CHANGES; ABC TRANSPORTER ARCHITECTURE; PRINCIPAL COMPONENT ANALYSIS;
D O I
10.1021/cr900095e
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A normal mode analysis (NMA) of biomolecular structures and functional mechanisms of membrane proteins was studied. Normal mode analysis provides information on the equilibrium modes accessible to a system, assuming that the system is stabilized by harmonic potentials. A striking feature of NMA and other PCAs of biomolecular structures is the observed robustness of the global modes to details in atomic coordinates or specific interatomic interactions. A major reason behind the broadening recognition of NMA as a tool for exploring functional motions of proteins is the observation that global modes elucidated by NMA bear functional significance. Membrane proteins are classified into two broad groups, integral membrane proteins (IMPs) and peripheral membrane proteins. The biological function of many membrane proteins involves a transient change in structure, with the associated processes usually spanning a broad range of time scales. The function of membrane proteins involves many other specific and subtle interactions that cannot be studied by CG models and NMA.
引用
收藏
页码:1463 / 1497
页数:35
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