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Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex
ATP-sensitive potassium (K(ATP)) channels are widely expressed and play key roles in many tissues by coupling metabolic state to membrane excitability. The SUR subunits confer drug and enhanced nucleotide sensitivity to the pore-forming Kir6 subunit, and so information transfer between the subunits...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Portland Press Ltd.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015859/ https://www.ncbi.nlm.nih.gov/pubmed/31957808 http://dx.doi.org/10.1042/BCJ20190753 |
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author | Brennan, Sean Rubaiy, Hussein N. Imanzadeh, Saba Reid, Ruth Lodwick, David Norman, Robert I. Rainbow, Richard D. |
author_facet | Brennan, Sean Rubaiy, Hussein N. Imanzadeh, Saba Reid, Ruth Lodwick, David Norman, Robert I. Rainbow, Richard D. |
author_sort | Brennan, Sean |
collection | PubMed |
description | ATP-sensitive potassium (K(ATP)) channels are widely expressed and play key roles in many tissues by coupling metabolic state to membrane excitability. The SUR subunits confer drug and enhanced nucleotide sensitivity to the pore-forming Kir6 subunit, and so information transfer between the subunits must occur. In our previous study, we identified an electrostatic interaction between Kir6 and SUR2 subunits that was key for allosteric information transfer between the regulatory and pore-forming subunit. In this study, we demonstrate a second putative interaction between Kir6.2-D323 and SUR2A-Q1336 using patch clamp electrophysiological recording, where charge swap mutation of the residues on either side of the potential interaction compromise normal channel function. The Kir6.2-D323K mutation gave rise to a constitutively active, glibenclamide and ATP-insensitive K(ATP) complex, further confirming the importance of information transfer between the Kir6 and SUR2 subunits. Sensitivity to modulators was restored when Kir6.2-D323K was co-expressed with a reciprocal charge swap mutant, SUR-Q1336E. Importantly, equivalent interactions have been identified in both Kir6.1 and Kir6.2 suggesting this is a second important interaction between Kir6 and the proximal C terminus of SUR. |
format | Online Article Text |
id | pubmed-7015859 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Portland Press Ltd. |
record_format | MEDLINE/PubMed |
spelling | pubmed-70158592020-02-24 Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex Brennan, Sean Rubaiy, Hussein N. Imanzadeh, Saba Reid, Ruth Lodwick, David Norman, Robert I. Rainbow, Richard D. Biochem J Biophysics ATP-sensitive potassium (K(ATP)) channels are widely expressed and play key roles in many tissues by coupling metabolic state to membrane excitability. The SUR subunits confer drug and enhanced nucleotide sensitivity to the pore-forming Kir6 subunit, and so information transfer between the subunits must occur. In our previous study, we identified an electrostatic interaction between Kir6 and SUR2 subunits that was key for allosteric information transfer between the regulatory and pore-forming subunit. In this study, we demonstrate a second putative interaction between Kir6.2-D323 and SUR2A-Q1336 using patch clamp electrophysiological recording, where charge swap mutation of the residues on either side of the potential interaction compromise normal channel function. The Kir6.2-D323K mutation gave rise to a constitutively active, glibenclamide and ATP-insensitive K(ATP) complex, further confirming the importance of information transfer between the Kir6 and SUR2 subunits. Sensitivity to modulators was restored when Kir6.2-D323K was co-expressed with a reciprocal charge swap mutant, SUR-Q1336E. Importantly, equivalent interactions have been identified in both Kir6.1 and Kir6.2 suggesting this is a second important interaction between Kir6 and the proximal C terminus of SUR. Portland Press Ltd. 2020-02-14 2020-02-11 /pmc/articles/PMC7015859/ /pubmed/31957808 http://dx.doi.org/10.1042/BCJ20190753 Text en © 2020 The Author(s) https://creativecommons.org/licenses/by/4.0/ This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution License 4.0 (CC BY) (https://creativecommons.org/licenses/by/4.0/) . Open access for this article was enabled by the participation of University of Liverpool in an all-inclusive Read & Publish pilot with Portland Press and the Biochemical Society under a transformative agreement with JISC. |
spellingShingle | Biophysics Brennan, Sean Rubaiy, Hussein N. Imanzadeh, Saba Reid, Ruth Lodwick, David Norman, Robert I. Rainbow, Richard D. Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex |
title | Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex |
title_full | Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex |
title_fullStr | Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex |
title_full_unstemmed | Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex |
title_short | Kir6.2-D323 and SUR2A-Q1336: an intersubunit interaction pairing for allosteric information transfer in the K(ATP) channel complex |
title_sort | kir6.2-d323 and sur2a-q1336: an intersubunit interaction pairing for allosteric information transfer in the k(atp) channel complex |
topic | Biophysics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7015859/ https://www.ncbi.nlm.nih.gov/pubmed/31957808 http://dx.doi.org/10.1042/BCJ20190753 |
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