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通过折叠和去折叠模拟得到的FSD-1的折叠过渡态和变性态系综。

Folding transition-state and denatured-state ensembles of FSD-1 from folding and unfolding simulations.

作者信息

Lei Hongxing, Dastidar Shubhra Ghosh, Duan Yong

机构信息

UC Davis Genome Center and Department of Applied Science, University of California, Davis, California 95616, USA.

出版信息

J Phys Chem B. 2006 Nov 2;110(43):22001-8. doi: 10.1021/jp063716a.

Abstract

Characterization of the folding transition-state ensemble and the denatured-state ensemble is an important step toward a full elucidation of protein folding mechanisms. We report herein an investigation of the free-energy landscape of FSD-1 protein by a total of four sets of folding and unfolding molecular dynamics simulations with explicit solvent. The transition-state ensemble was initially identified from unfolding simulations at 500 K and was verified by simulations at 300 K starting from the ensemble structures. The denatured-state ensemble and the early-stage folding were studied by a combination of unfolding simulations at 500 K and folding simulations at 300 K starting from the extended conformation. A common feature of the transition-state ensemble was the substantial formation of the native secondary structures, including both the alpha-helix and beta-sheet, with partial exposure of the hydrophobic core in the solvent. Both the native and non-native secondary structures were observed in the denatured-state ensemble and early-stage folding, consistent with the smooth experimental melting curve. Interestingly, the contact orders of the transition-state ensemble structures were similar to that of the native structure and were notably lower than those of the compact structures found in early-stage folding, implying that chain and topological entropy might play significant roles in protein folding. Implications for FSD-1 folding mechanisms and the rate-limiting step are discussed. Analyses further revealed interesting non-native interactions in the denatured-state ensemble and early-stage folding and the possibility that destabilization of these interactions could help to enhance the stability and folding rate of the protein.

摘要

表征折叠过渡态系综和变性态系综是全面阐明蛋白质折叠机制的重要一步。我们在此报告了通过总共四组含明确溶剂的折叠和展开分子动力学模拟对FSD-1蛋白自由能景观的研究。过渡态系综最初是从500 K的展开模拟中识别出来的,并通过从系综结构开始的300 K模拟进行了验证。变性态系综和早期折叠通过结合500 K的展开模拟和从伸展构象开始的300 K的折叠模拟进行研究。过渡态系综的一个共同特征是天然二级结构大量形成,包括α-螺旋和β-折叠,疏水核心在溶剂中有部分暴露。在变性态系综和早期折叠中都观察到了天然和非天然二级结构,这与平滑的实验熔解曲线一致。有趣的是,过渡态系综结构的接触序与天然结构相似,并且明显低于在早期折叠中发现的紧密结构的接触序,这意味着链熵和拓扑熵可能在蛋白质折叠中起重要作用。讨论了对FSD-1折叠机制和限速步骤的影响。分析进一步揭示了变性态系综和早期折叠中有趣的非天然相互作用,以及这些相互作用的不稳定可能有助于提高蛋白质稳定性和折叠速率的可能性。

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Differences in the folding transition state of ubiquitin indicated by phi and psi analyses.通过φ和ψ分析表明的泛素折叠过渡态的差异。
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