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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
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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. |
format | Online Article Text |
id | pubmed-8321532 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
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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