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Investigation of the conformational equilibration time of unfolded cytochrome c chains using time-resolved magnetic circular dichroism.

机译:使用时间分辨磁性圆二色性研究未折叠的细胞色素c链的构象平衡时间。

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摘要

The speed with which unfolded protein chains reach conformational equilibrium is a fundamental question in the study of protein folding. If unfolded chains reach equilibration on a time scale slower than protein folding, then it is possible to experimentally distinguish between a landscape folding mechanism and a classical folding mechanism. However, if unfolded chains reach equilibrium on a time scale faster than protein folding, folding proceeds from equilibrated conformations over a thermally activated barrier. Kinetic evidence is presented here for the first quantitative measurement of the rate of conformational equilibration from a folding-capable protein. The protein investigated in this work is the small globular protein, cytochrome c (cyt c), studied in the presence of guanidine hydrochloride (GndHCl) denaturant. The axial binding reactions of reduced cyt c's heme cofactor with histidine and methionine residues were monitored with time-resolved magnetic circular dichroism (TRMCD) spectroscopy after photodissociation of the CO complexes of unfolded protein obtained from horse and tuna, and from several histidine mutants of the horse protein. A kinetic model fitting both the reaction rate constants and spectra of the intermediates was used to obtain a quantitative estimate of the conformational diffusion time. The latter parameter was interpreted as a first-order time constant for exchange between conformational sub-ensembles presenting either a methionine or histidine residue to the heme iron for facile binding. The mean diffusional tau of the wild type and variants was 3 +/- 2 mus, close to the folding "speed limit" described recently in the literature. The implications of the relatively rapid conformational equilibration time observed are discussed in terms of the energy landscape and classical pathway time regimes of folding, for which the conformational diffusion time can be considered a pivotal point.
机译:展开的蛋白质链达到构象平衡的速度是蛋白质折叠研究中的一个基本问题。如果未折叠的链在比蛋白质折叠慢的时间尺度上达到平衡,则可以通过实验区分风景折叠机制和经典折叠机制。但是,如果未折叠的链在比蛋白折叠更快的时间尺度上达到平衡,则折叠将从热活化屏障上的平衡构象进行。此处提供了动力学证据,用于从可折叠蛋白质构象平衡速率的首次定量测量。在这项工作中研究的蛋白质是小球状蛋白质,细胞色素c(cyt c),是在盐酸胍(GndHCl)变性剂存在下研究的。还原的cyt c的血红素辅因子与组氨酸和蛋氨酸残基的轴向结合反应是用时间分辨的磁圆二色性(TRMCD)光谱监测的,该化合物是由马和金枪鱼以及几种金枪鱼的组氨酸突变体中获得的未折叠蛋白的CO络合物进行光解离后的。马蛋白。使用拟合反应速率常数和中间体光谱的动力学模型来获得构象扩散时间的定量估计。后一参数被解释为一阶时间常数,用于在向血红素铁呈递蛋氨酸或组氨酸残基以方便结合的构象子集合之间交换。野生型和变体的平均扩散tau为3 +/-2μs,接近文献中最近描述的折叠“速度极限”。观察到的相对较快的构象平衡时间的含义是根据能量态势和折叠的经典途径时间机制进行讨论的,对于它们而言,构象扩散时间可被视为关键点。

著录项

  • 作者

    Abel, Christina Janette.;

  • 作者单位

    University of California, Santa Cruz.;

  • 授予单位 University of California, Santa Cruz.;
  • 学科 Biophysics General.
  • 学位 Ph.D.
  • 年度 2006
  • 页码 133 p.
  • 总页数 133
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物物理学;
  • 关键词

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