蛋白质组学分析用于氨基酸错配检测:综述

Joana F Tavares, Filipe Assis-Santos, Manuel A. S. Santos
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引用次数: 1

摘要

蛋白质生物合成是一个对生命至关重要的高度精确的生物过程。氨基酸误译错误(误译)通常发生在低水平,但在氨基酸饥饿、暴露于药物、氧化应激和其他生理紊乱时会急剧增加。这些过程破坏蛋白质功能,通常被认为是有害的,然而,最近的研究表明,它们也可以被调节,在原核生物和真核生物中产生有利的表型。由于在识别和量化氨基酸误译方面的技术困难,人们对这种意外的适应性误译的生物学原理知之甚少。在这篇小型综述中,我们描述了蛋白质组规模的方法,包括使用质谱和生物信息学工具直接检测和量化误译事件,以及允许对位点特异性氨基酸变异进行敏感、灵活和低成本分析的间接功能方法。
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Proteomics Analysis for Amino Acid Misincorporation Detection: Mini Review
Protein biosynthesis is a highly accurate biological process essential for life. Amino acid misincorporation errors (mistranslation) normally occur at low levels, but can increase sharply upon amino acid starvation, exposure to drugs, oxidative stress and other physiological perturbations. These processes disrupt protein function and are normally regarded as being deleterious, however, recent work has shown that they can also be regulated to produce advantageous phenotypes in both prokaryotes and eukaryotes. The biology of such unexpected adaptive mistranslation is poorly understood due to technical difficulties in the identification and quantification of amino acid misincorporations. In this mini-review, we describe proteome scale methodologies involving the use of mass-spectrometry and bioinformatics tools to directly detect and quantify mistranslation events and also indirect functional methods that permit sensitive, flexible and low-cost analysis of site specific amino acid variation.
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