Analysis of PIN1WW domain through a simple statistical mechanics model

被引:6
作者
Bruscolini, P
Cecconi, F
机构
[1] Univ Zaragoza, Inst BIFI, E-50009 Zaragoza, Spain
[2] Univ Roma La Sapienza, Dipartimento Fis, I-00185 Rome, Italy
[3] INFM, Unita Roma 1, I-00185 Rome, Italy
关键词
protein folding; PIN1WW domain; statistical mechanics models; Monte Carlo simulations; mean field approximations; phi(T) values;
D O I
10.1016/j.bpc.2004.12.020
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have applied a simple statistical mechanics G (o) over bar -like model to the analysis of the PIN1 WW domain, resorting to mean field and Monte Carlo techniques to characterize its thermodynamics, and comparing the results with the wealth of available experimental data. PIN1 WW domain is a 39-residue protein fragment which folds on an antiparallel beta-sheet, thus representing an interesting model system to study the behavior of these secondary structure elements. Results show that the model correctly reproduces the two-state behavior of the protein, and also the trends of the experimental phi(T) values. Moreover, there is a good agreement between Monte Carlo results and the mean field ones, which can be obtained with a substantially smaller computational effort. (c) 2004 Elsevier B.V. All rights reserved.
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页码:153 / 158
页数:6
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