Life and death of Yfh1: how cool is cold denaturation

被引:1
作者
Temussi, Piero Andrea [1 ]
Martin, Stephen R. [2 ]
Pastore, Annalisa [3 ,4 ]
机构
[1] Univ Napoli Federico II, Naples, Italy
[2] Francis Crick Inst, London, England
[3] Elettra Sincrotrone Trieste, Basovizza, Italy
[4] Kings Coll London, Wohl Inst, London, England
关键词
biophysics; cold denaturation; energy landscape; folding funnel; frataxin; protein stability; YEAST FRATAXIN; FRIEDREICHS-ATAXIA; FUNCTIONAL INTERACTIONS; CRYSTAL-STRUCTURE; IRON-BINDING; PROTEIN; NMR; STABILITY; HEAT; MECHANISM;
D O I
10.1017/S0033583524000180
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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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页数:13
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