Role of naturally occurring osmolytes in protein folding and stability

被引:111
|
作者
Kumar, Raj [1 ]
机构
[1] Commonwealth Med Coll, Dept Basic Sci, Scranton, PA 18510 USA
关键词
Osmolyte; Protein folding; Protein structure; Cooperativity; Protein backbone; Amino acid side chain; INTRINSICALLY DISORDERED PROTEINS; NATIVELY UNFOLDED PROTEINS; ANDROGEN RECEPTOR; ORGANIC OSMOLYTES; MOLECULAR-BASIS; ALPHA-CHYMOTRYPSIN; UREA; STABILIZATION; BACKBONE; ENERGY;
D O I
10.1016/j.abb.2009.09.007
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
Osmolytes are typically accumulated in the intracellular environment at relatively high concentrations when cells/tissues are subjected to stress conditions. Osmolytes are common in a variety of organisms, including microorganisms, plants, and animals. They enhance thermodynamic stability of proteins by providing natively folded conformations without perturbing other cellular processes. By burying the backbone into the core of folded proteins, osmolytes can provide significant stability to proteins. Two properties of osmolytes are particularly important: (i) their ability to impart increased thermodynamic stability to folded proteins; and (ii) their compatibility in the intracellular environment at high concentrations. Under physiological conditions, the cellular compositions of osmolytes may vary significantly. This may lead to different protein folding pathways utilized in cells depending upon the intracellular environment. Proper understanding of the role of osmolytes in cell regulation should allow predicting the action of osmolytes on macromolecular interactions in stressed and crowded environments typical of cellular conditions. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:1 / 6
页数:6
相关论文
共 50 条