Structures of a peptide fragment Of β2-microglobulin studied by replica-exchange molecular dynamics simulations -: Towards the understanding of the mechanism of amyloid formation

被引:28
|
作者
Nishino, M
Sugita, Y
Yoda, T
Okamoto, Y [1 ]
机构
[1] Inst Mol Sci, Dept Theoret Studies, Okazaki, Aichi 4448585, Japan
[2] Natl Inst Mat Sci, Computat Mat Sci Ctr, Tsukuba, Ibaraki 3050047, Japan
[3] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan
[4] Nagahama Inst Biosci & Technol, Shiga 5260829, Japan
[5] Nagoya Univ, Grad Sch Sci, Dept Phys, Chikusa Ku, Nagoya, Aichi 4648602, Japan
关键词
amyloid fibrillogenesis; beta(2)-microglobulin; beta-hairpin; generalized ensemble algorithms; replica-exchange molecular dynamics;
D O I
10.1016/j.febslet.2005.08.068
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 investigate in detail the structural properties of the monomeric peptide fragment that corresponds to residues 21-31 of beta(2)-microglobulin. As a first step towards the understanding of the mechanism of the amyloid formation, we have performed a replica-exchange molecular dynamics simulation of this peptide with explicit water molecules. We analyze various structural properties as functions of temperature. Although the corresponding part of the native protein is a fully extended beta-strand, our results show that beta-hairpin structures are formed with high frequency around 310 K. We conjecture that this beta-hairpin formation is closely related to the amyloid fibrillogenesis. (c) 2005 Federation of European Biochemical Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:5425 / 5429
页数:5
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