corner
corner

Phys. Rev. Lett. 102, 218104 (2009) [4 pages]

Temperature Dependence of Normal Mode Reconstructions of Protein Dynamics

Download: PDF (803 kB) Buy this article Export: BibTeX or EndNote (RIS)

Francesco Piazza and Paolo De Los Rios
Laboratoire de Biophysique Statistique, SB ITP, Ecole Polytechnique Fédérale de Lausanne - EPFL, CH-1015, Lausanne, Switzerland

Fabio Cecconi
SMC-INFM Center for Statistical Mechanics and Complexity (CNR) and Istituto dei Sistemi Complessi CNR, Via dei Taurini 19, 00185 Rome, Italy.

Received 26 October 2008; published 29 May 2009

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.

© 2009 The American Physical Society

URL:
http://link.aps.org/doi/10.1103/PhysRevLett.102.218104
DOI:
10.1103/PhysRevLett.102.218104
PACS:
87.15.−v, 87.10.Tf, 87.14.E−