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Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm

The closing of the gated ion channel in the cystic fibrosis transmembrane conductance regulator can be categorized as nonpermissive to reopening, which involves the unbinding of ADP or ATP, or permissive, which does not. Identifying the type of closing is of interest as interactions with nucleotides...

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Detalles Bibliográficos
Autores principales: Moffett, Alexander S., Cui, Guiying, Thomas, Peter J., Hunt, William D., McCarty, Nael A., Westafer, Ryan S., Eckford, Andrew W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680790/
https://www.ncbi.nlm.nih.gov/pubmed/36425670
http://dx.doi.org/10.1016/j.bpr.2022.100083
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author Moffett, Alexander S.
Cui, Guiying
Thomas, Peter J.
Hunt, William D.
McCarty, Nael A.
Westafer, Ryan S.
Eckford, Andrew W.
author_facet Moffett, Alexander S.
Cui, Guiying
Thomas, Peter J.
Hunt, William D.
McCarty, Nael A.
Westafer, Ryan S.
Eckford, Andrew W.
author_sort Moffett, Alexander S.
collection PubMed
description The closing of the gated ion channel in the cystic fibrosis transmembrane conductance regulator can be categorized as nonpermissive to reopening, which involves the unbinding of ADP or ATP, or permissive, which does not. Identifying the type of closing is of interest as interactions with nucleotides can be affected in mutants or by introducing agonists. However, all closings are electrically silent and difficult to differentiate. For single-channel patch-clamp traces, we show that the type of the closing can be accurately determined by an inference algorithm implemented on a factor graph, which we demonstrate using both simulated and lab-obtained patch-clamp traces.
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spelling pubmed-96807902022-11-23 Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm Moffett, Alexander S. Cui, Guiying Thomas, Peter J. Hunt, William D. McCarty, Nael A. Westafer, Ryan S. Eckford, Andrew W. Biophys Rep (N Y) Report The closing of the gated ion channel in the cystic fibrosis transmembrane conductance regulator can be categorized as nonpermissive to reopening, which involves the unbinding of ADP or ATP, or permissive, which does not. Identifying the type of closing is of interest as interactions with nucleotides can be affected in mutants or by introducing agonists. However, all closings are electrically silent and difficult to differentiate. For single-channel patch-clamp traces, we show that the type of the closing can be accurately determined by an inference algorithm implemented on a factor graph, which we demonstrate using both simulated and lab-obtained patch-clamp traces. Elsevier 2022-10-19 /pmc/articles/PMC9680790/ /pubmed/36425670 http://dx.doi.org/10.1016/j.bpr.2022.100083 Text en © 2022 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Report
Moffett, Alexander S.
Cui, Guiying
Thomas, Peter J.
Hunt, William D.
McCarty, Nael A.
Westafer, Ryan S.
Eckford, Andrew W.
Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm
title Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm
title_full Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm
title_fullStr Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm
title_full_unstemmed Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm
title_short Permissive and nonpermissive channel closings in CFTR revealed by a factor graph inference algorithm
title_sort permissive and nonpermissive channel closings in cftr revealed by a factor graph inference algorithm
topic Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9680790/
https://www.ncbi.nlm.nih.gov/pubmed/36425670
http://dx.doi.org/10.1016/j.bpr.2022.100083
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