教授 博士生导师 硕士生导师
性别: 男
毕业院校: 东北师范大学
学位: 博士
所在单位: 生物工程学院
学科: 生物化工. 生物化学与分子生物学. 生物工程
办公地点: 生物工程学院401室
联系方式: 13624087256
电子邮箱: luanyush@dlut.edu.cn
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论文类型: 期刊论文
发表时间: 2012-07-01
发表刊物: INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
收录刊物: SCIE、PubMed
卷号: 51
期号: 1-2
页面范围: 113-118
ISSN号: 0141-8130
关键字: Human brain-type creatine kinase; Macromolecular crowding; Protein refolding; Aggregation
摘要: In this study, we quantitatively measured the effects of the macromolecular crowding agents, polyethylene glycol 2000 (PEG 2000), dextran 70, and calf thymus DNA (CT DNA), on the refolding and aggregation of recombinant human brain-type creatine kinase (rHBCK) denatured by guanidine hydrochloride (GdnHCl). The results showed that there is more aggregation in the presence of either a single crowding agent or in a mixture of crowding agents than in the absence of crowding agents, especially in the presence of a mixture containing CT DNA and PEG 2000 (or dextran 70). In the presence of high concentrations of PEG 2000 (100 g/L), dextran 70 (100 g/L), and CT DNA (15 g/L), the refolding yield remarkably decreased from 70% to 20%, 52% and 57%, respectively. A remarkable decrease in the refolding yield and rate with mixed crowding agent containing CT DNA and PEG 2000 (or dextran 70) was also observed. In comparison to refolding in the presence of 100 g/L PEG 2000, the refolding yields and rates improved in the presence of a mixture of PEG 2000 and dextran 70. We speculate that the crowding agents can favor both correct folding and misfolding/aggregation of denatured-rHBCK. Though it is not known what combination of crowding agents most accurately reflects the physiological environment within a cell, we believe our study could contribute to the understanding of protein folding and the factors that contribute to proper conformation and function in the intracellular environment. (c) 2012 Elsevier B.V. All rights reserved.