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Science. 2012 Apr 20;336(6079):362-6. doi: 10.1126/science.1214203.
2
Peptide chain dynamics in light and heavy water: zooming in on internal friction.轻水和重水中的肽链动力学:深入研究内摩擦。
J Am Chem Soc. 2012 Apr 11;134(14):6273-9. doi: 10.1021/ja211494h. Epub 2012 Mar 27.
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Solution structure of a minor and transiently formed state of a T4 lysozyme mutant.T4 溶菌酶突变体的次要且短暂形成状态的溶液结构。
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Nonnative interactions in the FF domain folding pathway from an atomic resolution structure of a sparsely populated intermediate: an NMR relaxation dispersion study.非天然相互作用在 FF 结构域折叠途径中的作用:从稀疏中间态的原子分辨率结构的 NMR 弛豫弥散研究。
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A transient and low-populated protein-folding intermediate at atomic resolution.原子分辨率下的短暂且低丰度蛋白质折叠中间体。
Science. 2010 Sep 10;329(5997):1312-6. doi: 10.1126/science.1191723.
6
Solvent viscosity and friction in protein folding dynamics.溶剂黏度和摩擦在蛋白质折叠动力学中的作用。
Curr Protein Pept Sci. 2010 Aug;11(5):385-95. doi: 10.2174/138920310791330596.
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Experimental evidence for a frustrated energy landscape in a three-helix-bundle protein family.三螺旋束蛋白家族中能量景观受阻的实验证据。
Nature. 2010 Feb 4;463(7281):685-8. doi: 10.1038/nature08743.
8
TALOS+: a hybrid method for predicting protein backbone torsion angles from NMR chemical shifts.TALOS+:一种利用核磁共振化学位移预测蛋白质主链扭转角的混合方法。
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9
Measuring internal friction of an ultrafast-folding protein.测量超快折叠蛋白质的内摩擦。
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10
Structures of invisible, excited protein states by relaxation dispersion NMR spectroscopy.利用弛豫色散核磁共振光谱法测定不可见激发态蛋白质的结构
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四螺旋束 FF 结构域从紧凑的沿途径中间态的折叠主要由水分子运动控制。

Folding of the four-helix bundle FF domain from a compact on-pathway intermediate state is governed predominantly by water motion.

机构信息

Departments of Molecular Genetics, Biochemistry and Chemistry, University of Toronto, Toronto, ON, Canada, M5S 1A8.

出版信息

Proc Natl Acad Sci U S A. 2012 Nov 20;109(47):19268-73. doi: 10.1073/pnas.1212036109. Epub 2012 Nov 5.

DOI:10.1073/pnas.1212036109
PMID:23129654
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3511121/
Abstract

Friction plays a critical role in protein folding. Frictional forces originating from random solvent and protein fluctuations both retard motion along the folding pathway and activate protein molecules to cross free energy barriers. Studies of friction thus may provide insights into the driving forces underlying protein conformational dynamics. However, the molecular origin of friction in protein folding remains poorly understood because, with the exception of the native conformer, there generally is little detailed structural information on the other states participating in the folding process. Here, we study the folding of the four-helix bundle FF domain that proceeds via a transiently formed, sparsely populated compact on-pathway folding intermediate whose structure was elucidated previously. Because the intermediate is stabilized by both native and nonnative interactions, friction in the folding transition between intermediate and folded states is expected to arise from intrachain reorganization in the protein. However, the viscosity dependencies of rates of folding from or unfolding to the intermediate, as established by relaxation dispersion NMR spectroscopy, clearly indicate that contributions from internal friction are small relative to those from solvent, so solvent frictional forces drive the folding process. Our results emphasize the importance of solvent dynamics in mediating the interconversion between protein configurations, even those that are highly compact, and in equilibrium folding/unfolding fluctuations in general.

摘要

摩擦在蛋白质折叠中起着关键作用。源自随机溶剂和蛋白质波动的摩擦力既会阻碍折叠途径中的运动,又会激活蛋白质分子跨越自由能势垒。因此,对摩擦力的研究可能有助于深入了解蛋白质构象动力学的驱动力。然而,由于除天然构象体外,其他参与折叠过程的状态通常很少有详细的结构信息,因此蛋白质折叠中摩擦力的分子起源仍未得到很好的理解。在这里,我们研究了四螺旋束 FF 结构域的折叠,该结构域通过一个短暂形成的、稀疏的紧凑的折叠中间体进行,该中间体的结构之前已经阐明。由于中间体是由天然和非天然相互作用稳定的,因此在中间体和折叠状态之间的折叠转变中摩擦力预计来自蛋白质内部的链内重组。然而,松弛分散 NMR 光谱学确定的从中性体折叠或去折叠的速率的粘度依赖性清楚地表明,与溶剂相比,内部摩擦力的贡献很小,因此溶剂摩擦力驱动折叠过程。我们的结果强调了溶剂动力学在介导蛋白质构象之间的相互转换,甚至是那些高度紧凑的构象以及一般的平衡折叠/去折叠波动中的重要性。