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How Cryo-EM Has Expanded Our Understanding of Membrane Transporters

Over the past two decades, technological advances in membrane protein structural biology have provided insight into the molecular mechanisms that transporters use to move diverse substrates across the membrane. However, the plasticity of these proteins’ ligand binding pockets, which allows them to b...

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Detalles Bibliográficos
Autores principales: Baril, Stefanie A., Gose, Tomoka, Schuetz, John D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society for Pharmacology and Experimental Therapeutics 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353158/
https://www.ncbi.nlm.nih.gov/pubmed/37438132
http://dx.doi.org/10.1124/dmd.122.001004
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author Baril, Stefanie A.
Gose, Tomoka
Schuetz, John D.
author_facet Baril, Stefanie A.
Gose, Tomoka
Schuetz, John D.
author_sort Baril, Stefanie A.
collection PubMed
description Over the past two decades, technological advances in membrane protein structural biology have provided insight into the molecular mechanisms that transporters use to move diverse substrates across the membrane. However, the plasticity of these proteins’ ligand binding pockets, which allows them to bind a range of substrates, also poses a challenge for drug development. Here we highlight the structure, function, and transport mechanism of ATP-binding cassette/solute carrier transporters that are related to several diseases and multidrug resistance: ABCB1, ABCC1, ABCG2, SLC19A1, and SLC29A1. SIGNIFICANCE STATEMENT: ATP-binding cassette transporters and solute carriers play vital roles in clinical chemotherapeutic outcomes. This paper describes the current understanding of the structure of five pharmacologically relevant transporters and how they interact with their ligands.
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spelling pubmed-103531582023-08-01 How Cryo-EM Has Expanded Our Understanding of Membrane Transporters Baril, Stefanie A. Gose, Tomoka Schuetz, John D. Drug Metab Dispos 50th Anniversary Celebration Collection Special Section on Perspective on Drug Metabolism and Disposition, Part II—Minireview Over the past two decades, technological advances in membrane protein structural biology have provided insight into the molecular mechanisms that transporters use to move diverse substrates across the membrane. However, the plasticity of these proteins’ ligand binding pockets, which allows them to bind a range of substrates, also poses a challenge for drug development. Here we highlight the structure, function, and transport mechanism of ATP-binding cassette/solute carrier transporters that are related to several diseases and multidrug resistance: ABCB1, ABCC1, ABCG2, SLC19A1, and SLC29A1. SIGNIFICANCE STATEMENT: ATP-binding cassette transporters and solute carriers play vital roles in clinical chemotherapeutic outcomes. This paper describes the current understanding of the structure of five pharmacologically relevant transporters and how they interact with their ligands. The American Society for Pharmacology and Experimental Therapeutics 2023-08 2023-08 /pmc/articles/PMC10353158/ /pubmed/37438132 http://dx.doi.org/10.1124/dmd.122.001004 Text en Copyright © 2023 by The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the CC BY Attribution 4.0 International license (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle 50th Anniversary Celebration Collection Special Section on Perspective on Drug Metabolism and Disposition, Part II—Minireview
Baril, Stefanie A.
Gose, Tomoka
Schuetz, John D.
How Cryo-EM Has Expanded Our Understanding of Membrane Transporters
title How Cryo-EM Has Expanded Our Understanding of Membrane Transporters
title_full How Cryo-EM Has Expanded Our Understanding of Membrane Transporters
title_fullStr How Cryo-EM Has Expanded Our Understanding of Membrane Transporters
title_full_unstemmed How Cryo-EM Has Expanded Our Understanding of Membrane Transporters
title_short How Cryo-EM Has Expanded Our Understanding of Membrane Transporters
title_sort how cryo-em has expanded our understanding of membrane transporters
topic 50th Anniversary Celebration Collection Special Section on Perspective on Drug Metabolism and Disposition, Part II—Minireview
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10353158/
https://www.ncbi.nlm.nih.gov/pubmed/37438132
http://dx.doi.org/10.1124/dmd.122.001004
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