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The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion
The Na(+)/K(+)-pump maintains the physiological K(+) and Na(+) electrochemical gradients across the cell membrane. It operates via an 'alternating-access' mechanism, making iterative transitions between inward-facing (E(1)) and outward-facing (E(2)) conformations. Although the general feat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026471/ https://www.ncbi.nlm.nih.gov/pubmed/27490484 http://dx.doi.org/10.7554/eLife.16616 |
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author | Rui, Huan Artigas, Pablo Roux, Benoît |
author_facet | Rui, Huan Artigas, Pablo Roux, Benoît |
author_sort | Rui, Huan |
collection | PubMed |
description | The Na(+)/K(+)-pump maintains the physiological K(+) and Na(+) electrochemical gradients across the cell membrane. It operates via an 'alternating-access' mechanism, making iterative transitions between inward-facing (E(1)) and outward-facing (E(2)) conformations. Although the general features of the transport cycle are known, the detailed physicochemical factors governing the binding site selectivity remain mysterious. Free energy molecular dynamics simulations show that the ion binding sites switch their binding specificity in E(1) and E(2). This is accompanied by small structural arrangements and changes in protonation states of the coordinating residues. Additional computations on structural models of the intermediate states along the conformational transition pathway reveal that the free energy barrier toward the occlusion step is considerably increased when the wrong type of ion is loaded into the binding pocket, prohibiting the pump cycle from proceeding forward. This self-correcting mechanism strengthens the overall transport selectivity and protects the stoichiometry of the pump cycle. DOI: http://dx.doi.org/10.7554/eLife.16616.001 |
format | Online Article Text |
id | pubmed-5026471 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-50264712016-09-20 The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion Rui, Huan Artigas, Pablo Roux, Benoît eLife Biophysics and Structural Biology The Na(+)/K(+)-pump maintains the physiological K(+) and Na(+) electrochemical gradients across the cell membrane. It operates via an 'alternating-access' mechanism, making iterative transitions between inward-facing (E(1)) and outward-facing (E(2)) conformations. Although the general features of the transport cycle are known, the detailed physicochemical factors governing the binding site selectivity remain mysterious. Free energy molecular dynamics simulations show that the ion binding sites switch their binding specificity in E(1) and E(2). This is accompanied by small structural arrangements and changes in protonation states of the coordinating residues. Additional computations on structural models of the intermediate states along the conformational transition pathway reveal that the free energy barrier toward the occlusion step is considerably increased when the wrong type of ion is loaded into the binding pocket, prohibiting the pump cycle from proceeding forward. This self-correcting mechanism strengthens the overall transport selectivity and protects the stoichiometry of the pump cycle. DOI: http://dx.doi.org/10.7554/eLife.16616.001 eLife Sciences Publications, Ltd 2016-08-04 /pmc/articles/PMC5026471/ /pubmed/27490484 http://dx.doi.org/10.7554/eLife.16616 Text en © 2016, Rui et al http://creativecommons.org/licenses/by/4.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biophysics and Structural Biology Rui, Huan Artigas, Pablo Roux, Benoît The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion |
title | The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion |
title_full | The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion |
title_fullStr | The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion |
title_full_unstemmed | The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion |
title_short | The selectivity of the Na(+)/K(+)-pump is controlled by binding site protonation and self-correcting occlusion |
title_sort | selectivity of the na(+)/k(+)-pump is controlled by binding site protonation and self-correcting occlusion |
topic | Biophysics and Structural Biology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5026471/ https://www.ncbi.nlm.nih.gov/pubmed/27490484 http://dx.doi.org/10.7554/eLife.16616 |
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