Cargando…

The genotype‐phenotype landscape of an allosteric protein

Allostery is a fundamental biophysical mechanism that underlies cellular sensing, signaling, and metabolism. Yet a quantitative understanding of allosteric genotype‐phenotype relationships remains elusive. Here, we report the large‐scale measurement of the genotype‐phenotype landscape for an alloste...

Descripción completa

Detalles Bibliográficos
Autores principales: Tack, Drew S, Tonner, Peter D, Pressman, Abe, Olson, Nathan D, Levy, Sasha F, Romantseva, Eugenia F, Alperovich, Nina, Vasilyeva, Olga, Ross, David
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009258/
https://www.ncbi.nlm.nih.gov/pubmed/33784029
http://dx.doi.org/10.15252/msb.202010179
_version_ 1783672844159287296
author Tack, Drew S
Tonner, Peter D
Pressman, Abe
Olson, Nathan D
Levy, Sasha F
Romantseva, Eugenia F
Alperovich, Nina
Vasilyeva, Olga
Ross, David
author_facet Tack, Drew S
Tonner, Peter D
Pressman, Abe
Olson, Nathan D
Levy, Sasha F
Romantseva, Eugenia F
Alperovich, Nina
Vasilyeva, Olga
Ross, David
author_sort Tack, Drew S
collection PubMed
description Allostery is a fundamental biophysical mechanism that underlies cellular sensing, signaling, and metabolism. Yet a quantitative understanding of allosteric genotype‐phenotype relationships remains elusive. Here, we report the large‐scale measurement of the genotype‐phenotype landscape for an allosteric protein: the lac repressor from Escherichia coli, LacI. Using a method that combines long‐read and short‐read DNA sequencing, we quantitatively measure the dose‐response curves for nearly 10(5) variants of the LacI genetic sensor. The resulting data provide a quantitative map of the effect of amino acid substitutions on LacI allostery and reveal systematic sequence‐structure‐function relationships. We find that in many cases, allosteric phenotypes can be quantitatively predicted with additive or neural‐network models, but unpredictable changes also occur. For example, we were surprised to discover a new band‐stop phenotype that challenges conventional models of allostery and that emerges from combinations of nearly silent amino acid substitutions.
format Online
Article
Text
id pubmed-8009258
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-80092582021-04-01 The genotype‐phenotype landscape of an allosteric protein Tack, Drew S Tonner, Peter D Pressman, Abe Olson, Nathan D Levy, Sasha F Romantseva, Eugenia F Alperovich, Nina Vasilyeva, Olga Ross, David Mol Syst Biol Articles Allostery is a fundamental biophysical mechanism that underlies cellular sensing, signaling, and metabolism. Yet a quantitative understanding of allosteric genotype‐phenotype relationships remains elusive. Here, we report the large‐scale measurement of the genotype‐phenotype landscape for an allosteric protein: the lac repressor from Escherichia coli, LacI. Using a method that combines long‐read and short‐read DNA sequencing, we quantitatively measure the dose‐response curves for nearly 10(5) variants of the LacI genetic sensor. The resulting data provide a quantitative map of the effect of amino acid substitutions on LacI allostery and reveal systematic sequence‐structure‐function relationships. We find that in many cases, allosteric phenotypes can be quantitatively predicted with additive or neural‐network models, but unpredictable changes also occur. For example, we were surprised to discover a new band‐stop phenotype that challenges conventional models of allostery and that emerges from combinations of nearly silent amino acid substitutions. John Wiley and Sons Inc. 2021-03-30 /pmc/articles/PMC8009258/ /pubmed/33784029 http://dx.doi.org/10.15252/msb.202010179 Text en © 2021 The Authors. Published under the terms of the CC BY 4.0 license This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Tack, Drew S
Tonner, Peter D
Pressman, Abe
Olson, Nathan D
Levy, Sasha F
Romantseva, Eugenia F
Alperovich, Nina
Vasilyeva, Olga
Ross, David
The genotype‐phenotype landscape of an allosteric protein
title The genotype‐phenotype landscape of an allosteric protein
title_full The genotype‐phenotype landscape of an allosteric protein
title_fullStr The genotype‐phenotype landscape of an allosteric protein
title_full_unstemmed The genotype‐phenotype landscape of an allosteric protein
title_short The genotype‐phenotype landscape of an allosteric protein
title_sort genotype‐phenotype landscape of an allosteric protein
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8009258/
https://www.ncbi.nlm.nih.gov/pubmed/33784029
http://dx.doi.org/10.15252/msb.202010179
work_keys_str_mv AT tackdrews thegenotypephenotypelandscapeofanallostericprotein
AT tonnerpeterd thegenotypephenotypelandscapeofanallostericprotein
AT pressmanabe thegenotypephenotypelandscapeofanallostericprotein
AT olsonnathand thegenotypephenotypelandscapeofanallostericprotein
AT levysashaf thegenotypephenotypelandscapeofanallostericprotein
AT romantsevaeugeniaf thegenotypephenotypelandscapeofanallostericprotein
AT alperovichnina thegenotypephenotypelandscapeofanallostericprotein
AT vasilyevaolga thegenotypephenotypelandscapeofanallostericprotein
AT rossdavid thegenotypephenotypelandscapeofanallostericprotein
AT tackdrews genotypephenotypelandscapeofanallostericprotein
AT tonnerpeterd genotypephenotypelandscapeofanallostericprotein
AT pressmanabe genotypephenotypelandscapeofanallostericprotein
AT olsonnathand genotypephenotypelandscapeofanallostericprotein
AT levysashaf genotypephenotypelandscapeofanallostericprotein
AT romantsevaeugeniaf genotypephenotypelandscapeofanallostericprotein
AT alperovichnina genotypephenotypelandscapeofanallostericprotein
AT vasilyevaolga genotypephenotypelandscapeofanallostericprotein
AT rossdavid genotypephenotypelandscapeofanallostericprotein