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: 2013-01-01
发表刊物: APPLIED BIOCHEMISTRY AND BIOTECHNOLOGY
收录刊物: SCIE、EI、PubMed、Scopus
卷号: 169
期号: 1
页面范围: 268-280
ISSN号: 0273-2289
关键字: Human brain-type creatine kinase; Macromolecular crowding; Guanidine; Hydrochloride denature; Inactivation; Kinetics
摘要: In this study, we quantitatively examined the effects of the macromolecular crowding agents, polyethylene glycol 2000 (PEG 2000) and dextran 70, on guanidine hydrochloride (GdnHCl)-induced denaturation of recombinant human brain-type creatine kinase (rHBCK). Our results showed that both PEG 2000 and dextran 70 had a protective effect on the inactivation of rHBCK induced by 0.5 M GdnHCl at 25 A degrees C. The presence of 200 g/L PEG 2000 resulted in the retention of 35.33 % of rHBCK activity after 4 h of inactivation, while no rHBCK activity was observed after denaturation in the absence of macromolecular crowding agents. The presence of PEG 2000 and dextran 70 at a concentration of 100 g/L could decelerate the k (2) value of the slow track to 21 and 33 %, respectively, in comparison to values obtained in the absence of crowding agents. Interestingly, inactivation of rHBCK in the presence of 200 g/L PEG 2000 followed first-order monophasic kinetics, with an apparent rate constant of 8 x 10(-5) s(-1). The intrinsic fluorescence results showed that PEG 2000 was better than dextran 70 at stabilizing rHBCK conformation. In addition, the results of the phase diagram indicate that more intermediates may be captured when rHBCK is denatured in a macromolecular crowding system. Mixed crowding agents did not produce better results than single crowding agents, but the protective effects of PEG 2000 on the inactivation and unfolding of rHBCK tended to increase as the ratio of PEG 2000 increased in the mixed crowding agent solution. Though it is not clear which crowding agents more accurately simulated the intracellular environment, this study could lead to a better understanding of protein unfolding in the intracellular environment.