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生物分子中的挫折感。

Frustration in biomolecules.

作者信息

Ferreiro Diego U, Komives Elizabeth A, Wolynes Peter G

机构信息

Protein Physiology Lab,Dep de Química Biológica,Facultad de Ciencias Exactas y Naturales,UBA-CONICET-IQUIBICEN,Buenos Aires,Argentina.

Department of Chemistry and Biochemistry,University of California San Diego,La Jolla,CA 92093,USA.

出版信息

Q Rev Biophys. 2014 Nov;47(4):285-363. doi: 10.1017/S0033583514000092. Epub 2014 Sep 16.

Abstract

Biomolecules are the prime information processing elements of living matter. Most of these inanimate systems are polymers that compute their own structures and dynamics using as input seemingly random character strings of their sequence, following which they coalesce and perform integrated cellular functions. In large computational systems with finite interaction-codes, the appearance of conflicting goals is inevitable. Simple conflicting forces can lead to quite complex structures and behaviors, leading to the concept of frustration in condensed matter. We present here some basic ideas about frustration in biomolecules and how the frustration concept leads to a better appreciation of many aspects of the architecture of biomolecules, and especially how biomolecular structure connects to function by means of localized frustration. These ideas are simultaneously both seductively simple and perilously subtle to grasp completely. The energy landscape theory of protein folding provides a framework for quantifying frustration in large systems and has been implemented at many levels of description. We first review the notion of frustration from the areas of abstract logic and its uses in simple condensed matter systems. We discuss then how the frustration concept applies specifically to heteropolymers, testing folding landscape theory in computer simulations of protein models and in experimentally accessible systems. Studying the aspects of frustration averaged over many proteins provides ways to infer energy functions useful for reliable structure prediction. We discuss how frustration affects folding mechanisms. We review here how the biological functions of proteins are related to subtle local physical frustration effects and how frustration influences the appearance of metastable states, the nature of binding processes, catalysis and allosteric transitions. In this review, we also emphasize that frustration, far from being always a bad thing, is an essential feature of biomolecules that allows dynamics to be harnessed for function. In this way, we hope to illustrate how Frustration is a fundamental concept in molecular biology.

摘要

生物分子是生命物质的主要信息处理元件。这些无生命系统中的大多数都是聚合物,它们利用自身序列看似随机的字符串作为输入来计算自身的结构和动力学,随后聚集并执行整合的细胞功能。在具有有限相互作用编码的大型计算系统中,相互冲突目标的出现是不可避免的。简单的相互冲突的力可导致相当复杂的结构和行为,从而引出凝聚态物质中的受挫概念。我们在此介绍一些关于生物分子中受挫现象的基本观点,以及受挫概念如何使人们更好地理解生物分子结构的诸多方面,特别是生物分子结构如何通过局部受挫与功能相联系。这些观点既诱人地简单,又微妙得难以完全理解。蛋白质折叠的能量景观理论为量化大型系统中的受挫现象提供了一个框架,并已在多个描述层面得以实现。我们首先回顾抽象逻辑领域中的受挫概念及其在简单凝聚态物质系统中的应用。然后我们讨论受挫概念如何具体应用于杂聚物,在蛋白质模型的计算机模拟以及实验可及的系统中检验折叠景观理论。研究多种蛋白质平均后的受挫方面为推断有助于可靠结构预测的能量函数提供了方法。我们讨论受挫如何影响折叠机制。我们在此回顾蛋白质的生物学功能如何与微妙的局部物理受挫效应相关,以及受挫如何影响亚稳态的出现、结合过程的性质、催化作用和别构转变。在本综述中,我们还强调,受挫远非总是坏事,而是生物分子的一个基本特征,它使动力学能够被用于实现功能。通过这种方式,我们希望说明受挫是分子生物学中的一个基本概念。

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50 years of allosteric interactions: the twists and turns of the models.50 年变构相互作用研究:模型的曲折历程。
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Native contacts determine protein folding mechanisms in atomistic simulations.天然接触决定原子模拟中的蛋白质折叠机制。
Proc Natl Acad Sci U S A. 2013 Oct 29;110(44):17874-9. doi: 10.1073/pnas.1311599110. Epub 2013 Oct 15.
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Designing cooperativity into the designed protein Top7.设计具有协同作用的人工设计蛋白 Top7。
Proteins. 2014 Mar;82(3):364-74. doi: 10.1002/prot.24393. Epub 2013 Oct 17.
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Diabetes mellitus due to the toxic misfolding of proinsulin variants.因胰岛素原变体的毒性错误折叠导致的糖尿病。
FEBS Lett. 2013 Jun 27;587(13):1942-50. doi: 10.1016/j.febslet.2013.04.044. Epub 2013 May 10.
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Correlated motions and residual frustration in thrombin.凝血酶中的关联运动和剩余挫折。
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