Cargando…
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...
Autores principales: | , , , , , |
---|---|
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 |
_version_ | 1785068693464547328 |
---|---|
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. |
format | Online Article Text |
id | pubmed-10322152 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT mitrovicdarko reconstructingthetransportcycleinthesugarportersuperfamilyusingcoevolutionpoweredmachinelearning AT mccomassarahe reconstructingthetransportcycleinthesugarportersuperfamilyusingcoevolutionpoweredmachinelearning AT allevaclaudia reconstructingthetransportcycleinthesugarportersuperfamilyusingcoevolutionpoweredmachinelearning AT bonaccorsimarta reconstructingthetransportcycleinthesugarportersuperfamilyusingcoevolutionpoweredmachinelearning AT drewdavid reconstructingthetransportcycleinthesugarportersuperfamilyusingcoevolutionpoweredmachinelearning AT delemottelucie reconstructingthetransportcycleinthesugarportersuperfamilyusingcoevolutionpoweredmachinelearning |