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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...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society for Pharmacology and Experimental Therapeutics
2023
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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. |
format | Online Article Text |
id | pubmed-10353158 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | The American Society for Pharmacology and Experimental Therapeutics |
record_format | MEDLINE/PubMed |
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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