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Originally published In Press as doi:10.1074/jbc.M409086200 on October 19, 2004

J. Biol. Chem., Vol. 279, Issue 53, 55109-55116, December 31, 2004
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Mixed Macromolecular Crowding Accelerates the Oxidative Refolding of Reduced, Denatured Lysozyme

IMPLICATIONS FOR PROTEIN FOLDING IN INTRACELLULAR ENVIRONMENTS*

Bing-Rui Zhou, Yi Liang{ddagger}, Fen Du, Zheng Zhou, and Jie Chen

From the National Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China

The oxidative refolding of reduced, denatured hen egg white lysozyme in the presence of a mixed macromolecular crowding agent containing both bovine serum albumin (BSA) and polysaccharide has been studied from a physiological point of view. When the total concentration of the mixed crowding agent is 100 g/liter, in which the weight ratio of BSA to dextran 70 is 1:9, the refolding yield of lysozyme after refolding for 4 h under this condition increases 24% compared with that in the presence of BSA and 16% compared with dextran 70. A remarkable increase in the refolding yield of lysozyme by a mixed crowding agent containing BSA and Ficoll 70 is also observed. Further folding kinetics analyses show that these two mixed crowding agents accelerate the oxidative refolding of lysozyme remarkably, compared with single crowding agents. These results suggest that the stabilization effects of mixed macromolecular crowding agents are stronger than those of single polysaccharide crowding agents such as dextran 70 and Ficoll 70, whereas the excluded volume effects of mixed macromolecular crowding agents are weaker than those of single protein crowding agents such as BSA. Both the refolding yield and the rate of the oxidative refolding of lysozyme in these two mixed crowded solutions with suitable weight ratios are higher than those in single crowded solutions, indicating that mixed macromolecular crowding agents are more favorable to lysozyme folding and can be used to simulate the intracellular environments more accurately than single crowding agents do.


Received for publication, August 9, 2004 , and in revised form, October 15, 2004.

* This work was supported by National Natural Science Foundation of China Grants 30370309 and 90408012, Project 863 Grant 2004AA404260, and Natural Science Foundation of Hubei Province Grant 2001abb046. The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked "advertisement" in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

{ddagger} To whom correspondence should be addressed: National Key Laboratory of Virology, College of Life Sciences, Wuhan University, Wuhan 430072, China. Tel.: 86-27-6875-4902; Fax: 86-27-6875-2560; E-mail: liangyi{at}whu.edu.cn.


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