Temperature Dependence of Normal Mode Reconstructions of Protein Dynamics

被引:19
|
作者
Piazza, Francesco [1 ]
De Los Rios, Paolo [1 ]
Cecconi, Fabio [2 ,3 ]
机构
[1] Ecole Polytech Fed Lausanne, Lab Biophys Stat, SB ITP, CH-1015 Lausanne, Switzerland
[2] CNR, Ctr Stat Mech & Complex, SMC INFM, I-00185 Rome, Italy
[3] CNR, Ist Sistemi Complessi, I-00185 Rome, Italy
关键词
D O I
10.1103/PhysRevLett.102.218104
中图分类号
O4 [物理学];
学科分类号
0702 ;
摘要
Normal mode (NM) analysis is a widely used technique for reconstructing conformational changes of proteins from the knowledge of native structures. In this Letter, we investigate to what extent NMs capture the salient features of the dynamics over a range of temperatures from close to T=0 to above unfolding. We show that the use of normal modes at room temperature is justified provided proteins are cooperative, that is, globular and highly structured. On the other hand, it is imperative to consider several modes in order to eliminate the unpredictable temperature dependence of single-mode contributions to the protein fluctuations.
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页数:4
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