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

被引:82
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.
引用
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页码:117 / 125
页数:9
相关论文
共 126 条
[71]   Trehalose favors a cutinase compact intermediate off-folding pathway [J].
Melo, EP ;
Chen, LY ;
Cabral, JMS ;
Fojan, P ;
Petersen, SB ;
Otzen, DE .
BIOCHEMISTRY, 2003, 42 (24) :7611-7617
[72]   Osmophobic effect of glycerol on irreversible thermal denaturation of rabbit creatine kinase [J].
Meng, FG ;
Hong, YK ;
He, HW ;
Lyubarev, AE ;
Kurganov, BI ;
Yan, YB ;
Zhou, HM .
BIOPHYSICAL JOURNAL, 2004, 87 (04) :2247-2254
[73]   Role of proline, glycerol, and heparin as protein folding aids during refolding of rabbit muscle creatine kinase [J].
Meng, FG ;
Park, YD ;
Zhou, HM .
INTERNATIONAL JOURNAL OF BIOCHEMISTRY & CELL BIOLOGY, 2001, 33 (07) :701-709
[75]  
MYERS JS, 1975, J BIOL CHEM, V250, P3785
[76]   DETERMINANTS OF RELATIVE AMOUNTS OF MEDULLARY ORGANIC OSMOLYTES - EFFECTS OF NACL AND UREA DIFFER [J].
NAKANISHI, T ;
UYAMA, O ;
NAKAHAMA, H ;
TAKAMITSU, Y ;
SUGITA, M .
AMERICAN JOURNAL OF PHYSIOLOGY, 1993, 264 (03) :F472-F479
[77]   The osmolyte betaine promotes protein misfolding and disruption of protein aggregates [J].
Natalello, Antonino ;
Liu, Jing ;
Ami, Diletta ;
Doglia, Silvia Maria ;
de Marco, Ario .
PROTEINS-STRUCTURE FUNCTION AND BIOINFORMATICS, 2009, 75 (02) :509-517
[78]   Effects of urea and trimethylamine-N-oxide (TMAO) on the interactions of lysozyme in solution [J].
Niebuhr, M ;
Koch, MHJ .
BIOPHYSICAL JOURNAL, 2005, 89 (03) :1978-1983
[79]   Comparative thermostability of glucose dehydrogenase from Haloferax mediterranei. Effects of salts and polyols [J].
Obon, JM ;
Manjon, A ;
Iborra, JL .
ENZYME AND MICROBIAL TECHNOLOGY, 1996, 19 (05) :352-360
[80]   Chemical chaperones reduce ER stress and restore glucose homeostasis in a mouse model of type 2 diabetes [J].
Oezcan, Umut ;
Yilmaz, Erkan ;
Oezcan, Lale ;
Furuhashi, Masato ;
Vaillancourt, Eric ;
Smith, Ross O. ;
Goerguen, Cem Z. ;
Hotamisligil, Goekhan S. .
SCIENCE, 2006, 313 (5790) :1137-1140