Cargando…
Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel
C-type inactivation is a process by which ion flux through a voltage-gated K(+) (K(v)) channel is regulated at the selectivity filter. While prior studies have indicated that C-type inactivation involves structural changes at the selectivity filter, the nature of the changes has not been resolved. H...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Association for the Advancement of Science
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032944/ https://www.ncbi.nlm.nih.gov/pubmed/35452285 http://dx.doi.org/10.1126/sciadv.abm8804 |
_version_ | 1784692769541849088 |
---|---|
author | Reddi, Ravikumar Matulef, Kimberly Riederer, Erika A. Whorton, Matthew R. Valiyaveetil, Francis I. |
author_facet | Reddi, Ravikumar Matulef, Kimberly Riederer, Erika A. Whorton, Matthew R. Valiyaveetil, Francis I. |
author_sort | Reddi, Ravikumar |
collection | PubMed |
description | C-type inactivation is a process by which ion flux through a voltage-gated K(+) (K(v)) channel is regulated at the selectivity filter. While prior studies have indicated that C-type inactivation involves structural changes at the selectivity filter, the nature of the changes has not been resolved. Here, we report the crystal structure of the K(v)1.2 channel in a C-type inactivated state. The structure shows that C-type inactivation involves changes in the selectivity filter that disrupt the outer two ion binding sites in the filter. The changes at the selectivity filter propagate to the extracellular mouth and the turret regions of the channel pore. The structural changes observed are consistent with the functional hallmarks of C-type inactivation. This study highlights the intricate interplay between K(+) occupancy at the ion binding sites and the interactions of the selectivity filter in determining the balance between the conductive and the inactivated conformations of the filter. |
format | Online Article Text |
id | pubmed-9032944 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Association for the Advancement of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-90329442022-05-04 Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel Reddi, Ravikumar Matulef, Kimberly Riederer, Erika A. Whorton, Matthew R. Valiyaveetil, Francis I. Sci Adv Biomedicine and Life Sciences C-type inactivation is a process by which ion flux through a voltage-gated K(+) (K(v)) channel is regulated at the selectivity filter. While prior studies have indicated that C-type inactivation involves structural changes at the selectivity filter, the nature of the changes has not been resolved. Here, we report the crystal structure of the K(v)1.2 channel in a C-type inactivated state. The structure shows that C-type inactivation involves changes in the selectivity filter that disrupt the outer two ion binding sites in the filter. The changes at the selectivity filter propagate to the extracellular mouth and the turret regions of the channel pore. The structural changes observed are consistent with the functional hallmarks of C-type inactivation. This study highlights the intricate interplay between K(+) occupancy at the ion binding sites and the interactions of the selectivity filter in determining the balance between the conductive and the inactivated conformations of the filter. American Association for the Advancement of Science 2022-04-22 /pmc/articles/PMC9032944/ /pubmed/35452285 http://dx.doi.org/10.1126/sciadv.abm8804 Text en Copyright © 2022 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC). https://creativecommons.org/licenses/by-nc/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution-NonCommercial license (https://creativecommons.org/licenses/by-nc/4.0/) , which permits use, distribution, and reproduction in any medium, so long as the resultant use is not for commercial advantage and provided the original work is properly cited. |
spellingShingle | Biomedicine and Life Sciences Reddi, Ravikumar Matulef, Kimberly Riederer, Erika A. Whorton, Matthew R. Valiyaveetil, Francis I. Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel |
title | Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel |
title_full | Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel |
title_fullStr | Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel |
title_full_unstemmed | Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel |
title_short | Structural basis for C-type inactivation in a Shaker family voltage-gated K(+) channel |
title_sort | structural basis for c-type inactivation in a shaker family voltage-gated k(+) channel |
topic | Biomedicine and Life Sciences |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9032944/ https://www.ncbi.nlm.nih.gov/pubmed/35452285 http://dx.doi.org/10.1126/sciadv.abm8804 |
work_keys_str_mv | AT reddiravikumar structuralbasisforctypeinactivationinashakerfamilyvoltagegatedkchannel AT matulefkimberly structuralbasisforctypeinactivationinashakerfamilyvoltagegatedkchannel AT riederererikaa structuralbasisforctypeinactivationinashakerfamilyvoltagegatedkchannel AT whortonmatthewr structuralbasisforctypeinactivationinashakerfamilyvoltagegatedkchannel AT valiyaveetilfrancisi structuralbasisforctypeinactivationinashakerfamilyvoltagegatedkchannel |