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

被引:429
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
相关论文
共 405 条
[1]  
Akke M, 1997, RNA, V3, P702
[2]   EFFECTS OF ION-BINDING ON THE BACKBONE DYNAMICS OF CALBINDIN-D9K DETERMINED BY N-15 NMR RELAXATION [J].
AKKE, M ;
SKELTON, NJ ;
KORDEL, J ;
PALMER, AG ;
CHAZIN, WJ .
BIOCHEMISTRY, 1993, 32 (37) :9832-9844
[3]   Pervasive conformational fluctuations on microsecond time scales in a fibronectin type III domain [J].
Akke, M ;
Liu, J ;
Cavanagh, J ;
Erickson, HP ;
Palmer, AG .
NATURE STRUCTURAL BIOLOGY, 1998, 5 (01) :55-59
[4]   Structural analysis of ion selectivity in the NaK channel [J].
Alam, Amer ;
Jiang, Youxing .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2009, 16 (01) :35-41
[5]   Ion permeation through a narrow channel: Using gramicidin to ascertain all-atom molecular dynamics potential of mean force methodology and biomolecular force fields [J].
Allen, TW ;
Andersen, OS ;
Roux, B .
BIOPHYSICAL JOURNAL, 2006, 90 (10) :3447-3468
[6]   Molecular dynamics study of the KcsA potassium channel [J].
Allen, TW ;
Kuyucak, S ;
Chung, SH .
BIOPHYSICAL JOURNAL, 1999, 77 (05) :2502-2516
[7]   Gramicidin A channel as a test ground for molecular dynamics force fields [J].
Allen, TW ;
Bastug, T ;
Kuyucak, S ;
Chung, SH .
BIOPHYSICAL JOURNAL, 2003, 84 (04) :2159-2168
[8]   Structural features and light-dependent changes in the cytoplasmic interhelical E-F loop region of rhodopsin: A site-directed spin-labeling study [J].
Altenbach, C ;
Yang, K ;
Farrens, DL ;
Farahbakhsh, ZT ;
Khorana, HG ;
Hubbell, WL .
BIOCHEMISTRY, 1996, 35 (38) :12470-12478
[9]   Structure and function in rhodopsin: Mapping light-dependent changes in distance between residue 316 in helix 8 and residues in the sequence 60-75, covering the cytoplasmic end of helices TM1 and TM2 and their connection loop CL1 [J].
Altenbach, C ;
Klein-Seetharaman, J ;
Cai, KW ;
Khorana, HG ;
Hubbell, WL .
BIOCHEMISTRY, 2001, 40 (51) :15493-15500
[10]   Structure and function in rhodopsin: Mapping light-dependent changes in distance between residue 65 in helix TM1 and residues in the sequence 306-319 at the cytoplasmic end of helix TM7 and in helix H8 [J].
Altenbach, C ;
Cai, KW ;
Klein-Seetharaman, J ;
Khorana, FG ;
Hubbell, WL .
BIOCHEMISTRY, 2001, 40 (51) :15483-15492