Yfh1的生与死:冷变性有多冷?

IF 7.2 2区 生物学 Q1 BIOPHYSICS Quarterly Reviews of Biophysics Pub Date : 2025-01-13 DOI:10.1017/S0033583524000180
Piero Andrea Temussi, Stephen R Martin, Annalisa Pastore
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引用次数: 0

摘要

酵母卵黄蛋白(Yfh1)是从酵母中提取的一种小的天然蛋白,它具有在低离子强度条件下在高于水冰点的温度下进行冷变性的不寻常特性。这种特性,加上显著的弹性,使得整个蛋白质和单个残基的稳定性曲线,即展开形式和折叠形式之间自由能差的温度依赖性,得以确定。无需添加变性剂或引入特别的不稳定突变,即可轻松测量稳定性曲线,使该蛋白质成为研究许多环境因素对蛋白质稳定性影响的理想“工具”。本综述旨在概括Yfh1已帮助解决的所有开放性问题,包括理解冷、热、压展开状态的差异和共性。因此,这种蛋白质为研究迄今为止被认为难以评估的蛋白质稳定性方面提供了一个独特的工具,并提供了重要的指导方针,可以允许识别其他类似的系统。
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Life and death of Yfh1: how cool is cold denaturation.

Yeast frataxin (Yfh1) is a small natural protein from yeast that has the unusual property of undergoing cold denaturation at temperatures above the freezing point of water when under conditions of low ionic strength. This peculiarity, together with remarkable resilience, allows the determination, for the whole protein as well as for individual residues, of the stability curve, that is the temperature dependence of the free energy difference between the unfolded and folded forms. The ease of measuring stability curves without the need to add denaturants or introduce ad hoc destabilizing mutations makes this protein an ideal 'tool' for investigating the influence of many environmental factors on protein stability. The present review aims at recapitulating all the open questions that Yfh1 has helped to address, including understanding the differences and commonalities of the cold, heat and pressure unfolded states. This protein thus offers a unique tool for studying aspects of protein stability so far been considered difficult to assess and provides important guidelines that could allow the identification of other similar systems.

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来源期刊
Quarterly Reviews of Biophysics
Quarterly Reviews of Biophysics 生物-生物物理
CiteScore
12.90
自引率
1.60%
发文量
16
期刊介绍: Quarterly Reviews of Biophysics covers the field of experimental and computational biophysics. Experimental biophysics span across different physics-based measurements such as optical microscopy, super-resolution imaging, electron microscopy, X-ray and neutron diffraction, spectroscopy, calorimetry, thermodynamics and their integrated uses. Computational biophysics includes theory, simulations, bioinformatics and system analysis. These biophysical methodologies are used to discover the structure, function and physiology of biological systems in varying complexities from cells, organelles, membranes, protein-nucleic acid complexes, molecular machines to molecules. The majority of reviews published are invited from authors who have made significant contributions to the field, who give critical, readable and sometimes controversial accounts of recent progress and problems in their specialty. The journal has long-standing, worldwide reputation, demonstrated by its high ranking in the ISI Science Citation Index, as a forum for general and specialized communication between biophysicists working in different areas. Thematic issues are occasionally published.
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