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通过分析数千个变体对活性和丰度的影响来了解蛋白质功能丧失的起源。

Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance.

机构信息

Linderstrøm-Lang Centre for Protein Science, Department of Biology, University of Copenhagen, Copenhagen, Denmark.

Department of Pharmaceutical Sciences, St. Jude Children's Research Hospital, Memphis, TN, USA.

出版信息

Mol Biol Evol. 2021 Jul 29;38(8):3235-3246. doi: 10.1093/molbev/msab095.

Abstract

Understanding and predicting how amino acid substitutions affect proteins are keys to our basic understanding of protein function and evolution. Amino acid changes may affect protein function in a number of ways including direct perturbations of activity or indirect effects on protein folding and stability. We have analyzed 6,749 experimentally determined variant effects from multiplexed assays on abundance and activity in two proteins (NUDT15 and PTEN) to quantify these effects and find that a third of the variants cause loss of function, and about half of loss-of-function variants also have low cellular abundance. We analyze the structural and mechanistic origins of loss of function and use the experimental data to find residues important for enzymatic activity. We performed computational analyses of protein stability and evolutionary conservation and show how we may predict positions where variants cause loss of activity or abundance. In this way, our results link thermodynamic stability and evolutionary conservation to experimental studies of different properties of protein fitness landscapes.

摘要

理解和预测氨基酸取代如何影响蛋白质是我们对蛋白质功能和进化的基本理解的关键。氨基酸变化可能会以多种方式影响蛋白质功能,包括直接干扰活性或间接影响蛋白质折叠和稳定性。我们分析了在两个蛋白质(NUDT15 和 PTEN)中进行的丰度和活性的多重测定实验中确定的 6749 个变体效应,以量化这些效应,并发现三分之一的变体导致功能丧失,而大约一半的功能丧失变体的细胞丰度也较低。我们分析了功能丧失的结构和机制起源,并利用实验数据找到对酶活性重要的残基。我们对蛋白质稳定性和进化保守性进行了计算分析,并展示了如何预测导致活性或丰度丧失的变体位置。通过这种方式,我们的结果将热力学稳定性和进化保守性与蛋白质适应性景观不同性质的实验研究联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dea4/8321532/4dceb1639c64/msab095f1.jpg

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