Protein and DNA destabilization by osmolytes: The other side of the coin

被引:81
|
作者
Singh, Laishram R. [1 ]
Poddar, Nitesh Kumar [1 ]
Dar, Tanveer Ali [2 ]
Kumar, Raj [3 ]
Ahmad, Faizan [1 ]
机构
[1] Jamia Millia Islamia, Ctr Interdisciplinary Res Basic Sci, New Delhi 110025, India
[2] Baba Ghulam Shah Badshah Univ, Sch Biosci & Biotechnol, Rajouri 185131, Jammu & Kashmir, India
[3] Commonwealth Med Coll, Dept Basic Sci, Scranton, PA 18510 USA
关键词
Osmolyte; Preferential hydration; Protein stabilization; Protein destabilization; Protein folding; TRIMETHYLAMINE-N-OXIDE; IRREVERSIBLE THERMAL-DENATURATION; CHEMICAL CHAPERONES; GLYCINE BETAINE; GIBBS ENERGY; PREFERENTIAL INTERACTIONS; CONFORMATIONAL-CHANGES; LACTATE-DEHYDROGENASE; ESCHERICHIA-COLI; COMPATIBLE OSMOLYTE;
D O I
10.1016/j.lfs.2010.10.020
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
Osmolytes are naturally occurring small molecules accumulated intracellularly to protect organisms from various denaturing stresses. Similar to the two faces of a coin, several of these osmolytes are stabilizing and destabilizing proteins depending on the concentrations and/or solvent conditions. For example, the well known stabilizing osmolyte, trehalose destabilizes some proteins at high concentration and/or high pH. In spite of the fact that destabilizing aspects of osmolytes can modulate many cellular processes including regulation of protein homeostasis (proteostasis), protein-protein interaction, and protein-DNA interaction, researchers have mostly focused on the stabilizing aspects of osmolytes. Thus, it is important to look into both aspects of osmolytes to determine their precise role under physiological conditions. In this article, we have discussed both stabilizing and destabilizing/denaturant aspects of osmolytes to uncover both sides of the coin. (C) 2010 Elsevier Inc. All rights reserved.
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页码:117 / 125
页数:9
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