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Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning

Sugar porters (SPs) represent the largest group of secondary-active transporters. Some members, such as the glucose transporters (GLUTs), are well known for their role in maintaining blood glucose homeostasis in mammals, with their expression upregulated in many types of cancers. Because only a few...

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Autores principales: Mitrovic, Darko, McComas, Sarah E, Alleva, Claudia, Bonaccorsi, Marta, Drew, David, Delemotte, Lucie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322152/
https://www.ncbi.nlm.nih.gov/pubmed/37405846
http://dx.doi.org/10.7554/eLife.84805
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author Mitrovic, Darko
McComas, Sarah E
Alleva, Claudia
Bonaccorsi, Marta
Drew, David
Delemotte, Lucie
author_facet Mitrovic, Darko
McComas, Sarah E
Alleva, Claudia
Bonaccorsi, Marta
Drew, David
Delemotte, Lucie
author_sort Mitrovic, Darko
collection PubMed
description Sugar porters (SPs) represent the largest group of secondary-active transporters. Some members, such as the glucose transporters (GLUTs), are well known for their role in maintaining blood glucose homeostasis in mammals, with their expression upregulated in many types of cancers. Because only a few sugar porter structures have been determined, mechanistic models have been constructed by piecing together structural states of distantly related proteins. Current GLUT transport models are predominantly descriptive and oversimplified. Here, we have combined coevolution analysis and comparative modeling, to predict structures of the entire sugar porter superfamily in each state of the transport cycle. We have analyzed the state-specific contacts inferred from coevolving residue pairs and shown how this information can be used to rapidly generate free-energy landscapes consistent with experimental estimates, as illustrated here for the mammalian fructose transporter GLUT5. By comparing many different sugar porter models and scrutinizing their sequence, we have been able to define the molecular determinants of the transport cycle, which are conserved throughout the sugar porter superfamily. We have also been able to highlight differences leading to the emergence of proton-coupling, validating, and extending the previously proposed latch mechanism. Our computational approach is transferable to any transporter, and to other protein families in general.
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spelling pubmed-103221522023-07-06 Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning Mitrovic, Darko McComas, Sarah E Alleva, Claudia Bonaccorsi, Marta Drew, David Delemotte, Lucie eLife Structural Biology and Molecular Biophysics Sugar porters (SPs) represent the largest group of secondary-active transporters. Some members, such as the glucose transporters (GLUTs), are well known for their role in maintaining blood glucose homeostasis in mammals, with their expression upregulated in many types of cancers. Because only a few sugar porter structures have been determined, mechanistic models have been constructed by piecing together structural states of distantly related proteins. Current GLUT transport models are predominantly descriptive and oversimplified. Here, we have combined coevolution analysis and comparative modeling, to predict structures of the entire sugar porter superfamily in each state of the transport cycle. We have analyzed the state-specific contacts inferred from coevolving residue pairs and shown how this information can be used to rapidly generate free-energy landscapes consistent with experimental estimates, as illustrated here for the mammalian fructose transporter GLUT5. By comparing many different sugar porter models and scrutinizing their sequence, we have been able to define the molecular determinants of the transport cycle, which are conserved throughout the sugar porter superfamily. We have also been able to highlight differences leading to the emergence of proton-coupling, validating, and extending the previously proposed latch mechanism. Our computational approach is transferable to any transporter, and to other protein families in general. eLife Sciences Publications, Ltd 2023-07-05 /pmc/articles/PMC10322152/ /pubmed/37405846 http://dx.doi.org/10.7554/eLife.84805 Text en © 2023, Mitrovic et al https://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Structural Biology and Molecular Biophysics
Mitrovic, Darko
McComas, Sarah E
Alleva, Claudia
Bonaccorsi, Marta
Drew, David
Delemotte, Lucie
Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
title Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
title_full Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
title_fullStr Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
title_full_unstemmed Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
title_short Reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
title_sort reconstructing the transport cycle in the sugar porter superfamily using coevolution-powered machine learning
topic Structural Biology and Molecular Biophysics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10322152/
https://www.ncbi.nlm.nih.gov/pubmed/37405846
http://dx.doi.org/10.7554/eLife.84805
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