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通过天然蛋白质中几乎每个主链氢键处的EX1型氢交换揭示的微秒到分钟级动力学。

Microsecond to minute dynamics revealed by EX1-type hydrogen exchange at nearly every backbone hydrogen bond in a native protein.

作者信息

Arrington C B, Robertson A D

机构信息

Department of Biochemistry, the University of Iowa, Iowa City 52242, USA.

出版信息

J Mol Biol. 2000 Mar 10;296(5):1307-17. doi: 10.1006/jmbi.2000.3536.

Abstract

A previous comprehensive analysis of the pH dependence of native-state amide hydrogen (NH) exchange in turkey ovomucoid third domain (OMTKY3) yielded apparent opening and closing rate constants (k(op) and k(cl)) at 14 NH groups involved in global conformational changes. This analysis has been extended to 18 additional slowly exchanging NH groups. Quench-flow experiments were performed to monitor NH exchange in native OMTKY3 from neutral to very alkaline pH ( approximately 12) conditions. Above pH 10 the mechanism of exchange switched from one governed by a rapid equilibrium preceding the chemistry of exchange (i.e. EX2 exchange), to one where exchange was limited by the rate of opening (i.e. EX1 exchange). Kinetics of solvent exposure are now known for nearly all backbone NH groups in native OMTKY3, yielding rate constants that span five orders of magnitude, 0.004 to 200 s(-1).

摘要

之前对火鸡卵类粘蛋白第三结构域(OMTKY3)天然态酰胺氢(NH)交换的pH依赖性进行的全面分析,得出了参与全局构象变化的14个NH基团的明显打开和关闭速率常数(k(op)和k(cl))。该分析已扩展到另外18个缓慢交换的NH基团。进行了淬灭流动实验,以监测天然OMTKY3在从中性到非常碱性的pH(约12)条件下的NH交换。在pH 10以上,交换机制从由交换化学之前的快速平衡控制的机制(即EX2交换)转变为交换受打开速率限制的机制(即EX1交换)。现在已知天然OMTKY3中几乎所有主链NH基团的溶剂暴露动力学,得出的速率常数跨越五个数量级,从0.004到200 s(-1)。

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