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探针依赖的非指数弛豫动力学:蛋白质向下折叠的不可靠特征

Probe-dependent and nonexponential relaxation kinetics: unreliable signatures of downhill protein folding.

作者信息

Hagen Stephen J

机构信息

Department of Physics, University of Florida, Gainesville, Florida 32611-8440, USA.

出版信息

Proteins. 2007 Jul 1;68(1):205-17. doi: 10.1002/prot.21342.

Abstract

The theoretical suggestion that some proteins may encounter no significant free energy barriers during their folding raises an important question: What experimental signature does this downhill folding produce? Several authors have argued that nonexponential (and especially stretched exponential) or probe-dependent kinetics represent useful experimental signatures of a downhill free energy surface. Here we examine more closely the connection between unusual kinetics and downhill energy surfaces. Simulation of diffusive relaxation dynamics on a variety of generically downhill, two-dimensional free energy surfaces shows that these surfaces do not necessarily produce either probe-dependent or significantly nonexponential kinetics. Conversely, we find that two-dimensional surfaces with significant (>3 k(B) T) energy barriers can readily give rise to nonexponential and probe-dependent kinetics. These results show that downhill folding does not constitute a necessary or sufficient condition for nonexponential and/or probe-dependent folding kinetics. One cannot easily prove or disprove that a protein folds downhill simply by studying its relaxation kinetics.

摘要

一些蛋白质在折叠过程中可能不会遇到显著的自由能障碍这一理论观点引发了一个重要问题

这种下坡式折叠会产生怎样的实验特征呢?几位作者认为,非指数(尤其是拉伸指数)或探针依赖动力学是下坡自由能表面的有用实验特征。在这里,我们更深入地研究异常动力学与下坡能量表面之间的联系。在各种一般为下坡的二维自由能表面上对扩散弛豫动力学进行模拟表明,这些表面不一定会产生探针依赖或显著的非指数动力学。相反,我们发现具有显著(>3k(B)T)能量障碍的二维表面很容易产生非指数和探针依赖动力学。这些结果表明,下坡折叠对于非指数和/或探针依赖的折叠动力学既不是必要条件也不是充分条件。仅仅通过研究蛋白质的弛豫动力学,很难证明或反驳其是否以下坡方式折叠。

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