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

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 st...

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Autores principales: Cagiada, Matteo, Johansson, Kristoffer E, Valanciute, Audrone, Nielsen, Sofie V, Hartmann-Petersen, Rasmus, Yang, Jun J, Fowler, Douglas M, Stein, Amelie, Lindorff-Larsen, Kresten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321532/
https://www.ncbi.nlm.nih.gov/pubmed/33779753
http://dx.doi.org/10.1093/molbev/msab095
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author Cagiada, Matteo
Johansson, Kristoffer E
Valanciute, Audrone
Nielsen, Sofie V
Hartmann-Petersen, Rasmus
Yang, Jun J
Fowler, Douglas M
Stein, Amelie
Lindorff-Larsen, Kresten
author_facet Cagiada, Matteo
Johansson, Kristoffer E
Valanciute, Audrone
Nielsen, Sofie V
Hartmann-Petersen, Rasmus
Yang, Jun J
Fowler, Douglas M
Stein, Amelie
Lindorff-Larsen, Kresten
author_sort Cagiada, Matteo
collection PubMed
description 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.
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spelling pubmed-83215322021-07-30 Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance Cagiada, Matteo Johansson, Kristoffer E Valanciute, Audrone Nielsen, Sofie V Hartmann-Petersen, Rasmus Yang, Jun J Fowler, Douglas M Stein, Amelie Lindorff-Larsen, Kresten Mol Biol Evol Discoveries 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. Oxford University Press 2021-03-29 /pmc/articles/PMC8321532/ /pubmed/33779753 http://dx.doi.org/10.1093/molbev/msab095 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) ), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Discoveries
Cagiada, Matteo
Johansson, Kristoffer E
Valanciute, Audrone
Nielsen, Sofie V
Hartmann-Petersen, Rasmus
Yang, Jun J
Fowler, Douglas M
Stein, Amelie
Lindorff-Larsen, Kresten
Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance
title Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance
title_full Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance
title_fullStr Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance
title_full_unstemmed Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance
title_short Understanding the Origins of Loss of Protein Function by Analyzing the Effects of Thousands of Variants on Activity and Abundance
title_sort understanding the origins of loss of protein function by analyzing the effects of thousands of variants on activity and abundance
topic Discoveries
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8321532/
https://www.ncbi.nlm.nih.gov/pubmed/33779753
http://dx.doi.org/10.1093/molbev/msab095
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