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Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering
Pentameric ligand-gated ion channels undergo subtle conformational cycling to control electrochemical signal transduction in many kingdoms of life. Several crystal structures have now been reported in this family, but the functional relevance of such models remains unclear. Here, we used small-angle...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
National Academy of Sciences
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449418/ https://www.ncbi.nlm.nih.gov/pubmed/34504004 http://dx.doi.org/10.1073/pnas.2108006118 |
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author | Lycksell, Marie Rovšnik, Urška Bergh, Cathrine Johansen, Nicolai T. Martel, Anne Porcar, Lionel Arleth, Lise Howard, Rebecca J. Lindahl, Erik |
author_facet | Lycksell, Marie Rovšnik, Urška Bergh, Cathrine Johansen, Nicolai T. Martel, Anne Porcar, Lionel Arleth, Lise Howard, Rebecca J. Lindahl, Erik |
author_sort | Lycksell, Marie |
collection | PubMed |
description | Pentameric ligand-gated ion channels undergo subtle conformational cycling to control electrochemical signal transduction in many kingdoms of life. Several crystal structures have now been reported in this family, but the functional relevance of such models remains unclear. Here, we used small-angle neutron scattering (SANS) to probe ambient solution-phase properties of the pH-gated bacterial ion channel GLIC under resting and activating conditions. Data collection was optimized by inline paused-flow size-exclusion chromatography, and exchanging into deuterated detergent to hide the micelle contribution. Resting-state GLIC was the best-fit crystal structure to SANS curves, with no evidence for divergent mechanisms. Moreover, enhanced-sampling molecular-dynamics simulations enabled differential modeling in resting versus activating conditions, with the latter corresponding to an intermediate ensemble of both the extracellular and transmembrane domains. This work demonstrates state-dependent changes in a pentameric ion channel by SANS, an increasingly accessible method for macromolecular characterization with the coming generation of neutron sources. |
format | Online Article Text |
id | pubmed-8449418 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | National Academy of Sciences |
record_format | MEDLINE/PubMed |
spelling | pubmed-84494182021-10-04 Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering Lycksell, Marie Rovšnik, Urška Bergh, Cathrine Johansen, Nicolai T. Martel, Anne Porcar, Lionel Arleth, Lise Howard, Rebecca J. Lindahl, Erik Proc Natl Acad Sci U S A Biological Sciences Pentameric ligand-gated ion channels undergo subtle conformational cycling to control electrochemical signal transduction in many kingdoms of life. Several crystal structures have now been reported in this family, but the functional relevance of such models remains unclear. Here, we used small-angle neutron scattering (SANS) to probe ambient solution-phase properties of the pH-gated bacterial ion channel GLIC under resting and activating conditions. Data collection was optimized by inline paused-flow size-exclusion chromatography, and exchanging into deuterated detergent to hide the micelle contribution. Resting-state GLIC was the best-fit crystal structure to SANS curves, with no evidence for divergent mechanisms. Moreover, enhanced-sampling molecular-dynamics simulations enabled differential modeling in resting versus activating conditions, with the latter corresponding to an intermediate ensemble of both the extracellular and transmembrane domains. This work demonstrates state-dependent changes in a pentameric ion channel by SANS, an increasingly accessible method for macromolecular characterization with the coming generation of neutron sources. National Academy of Sciences 2021-09-14 2021-09-09 /pmc/articles/PMC8449418/ /pubmed/34504004 http://dx.doi.org/10.1073/pnas.2108006118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by/4.0/This open access article is distributed under Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biological Sciences Lycksell, Marie Rovšnik, Urška Bergh, Cathrine Johansen, Nicolai T. Martel, Anne Porcar, Lionel Arleth, Lise Howard, Rebecca J. Lindahl, Erik Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering |
title | Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering |
title_full | Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering |
title_fullStr | Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering |
title_full_unstemmed | Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering |
title_short | Probing solution structure of the pentameric ligand-gated ion channel GLIC by small-angle neutron scattering |
title_sort | probing solution structure of the pentameric ligand-gated ion channel glic by small-angle neutron scattering |
topic | Biological Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8449418/ https://www.ncbi.nlm.nih.gov/pubmed/34504004 http://dx.doi.org/10.1073/pnas.2108006118 |
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