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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...

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Autores principales: Lycksell, Marie, Rovšnik, Urška, Bergh, Cathrine, Johansen, Nicolai T., Martel, Anne, Porcar, Lionel, Arleth, Lise, Howard, Rebecca J., Lindahl, Erik
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
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.
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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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