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dc.contributor.author
Meyer, Dylan J.
dc.contributor.author
Bijlani, Sharan
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de Sautu, Marilina
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dc.contributor.author
Spontarelli, Kerri
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Young, Victoria C.
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Gatto, Craig
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Artigas, Pablo
dc.date.available
2021-05-27T11:54:12Z
dc.date.issued
2020-12
dc.identifier.citation
Meyer, Dylan J.; Bijlani, Sharan; de Sautu, Marilina; Spontarelli, Kerri; Young, Victoria C.; et al.; FXYD protein isoforms differentially modulate human Na/K pump function; Rockefeller University Press; Journal Of General Physiology; 152; 12; 12-2020; 1-21
dc.identifier.issn
0022-1295
dc.identifier.uri
http://hdl.handle.net/11336/132637
dc.description.abstract
Tight regulation of the Na/K pump is essential for cellular function because this heteromeric protein builds and maintains the electrochemical gradients for Na+ and K+ that energize electrical signaling and secondary active transport. We studied the regulation of the ubiquitous human α1β1 pump isoform by five human FXYD proteins normally located in muscle, kidney, and neurons. The function of Na/K pump α1β1 expressed in Xenopus oocytes with or without FXYD isoforms was evaluated using two-electrode voltage clamp and patch clamp. Through evaluation of the partial reactions in the absence of K+ but presence of Na+ in the external milieu, we demonstrate that each FXYD subunit alters the equilibrium between E1P(3Na) and E2P, the phosphorylated conformations with Na+ occluded and free from Na+, respectively, thereby altering the apparent affinity for Na+. This modification of Na+ interaction shapes the small effects of FXYD proteins on the apparent affinity for external K+ at physiological Na+. FXYD6 distinctively accelerated both the Na+-deocclusion and the pump-turnover rates. All FXYD isoforms altered the apparent affinity for intracellular Na+ in patches, an effect that was observed only in the presence of intracellular K+. Therefore, FXYD proteins alter the selectivity of the pump for intracellular ions, an effect that could be due to the altered equilibrium between E1 and E2, the two major pump conformations, and/or to small changes in ion affinities that are exacerbated when both ions are present. Lastly, we observed a drastic reduction of Na/K pump surface expression when it was coexpressed with FXYD1 or FXYD6, with the former being relieved by injection of PKA's catalytic subunit into the oocyte. Our results indicate that a prominent effect of FXYD1 and FXYD6, and plausibly other FXYDs, is the regulation of Na/K pump trafficking.
dc.format
application/pdf
dc.language.iso
eng
dc.publisher
Rockefeller University Press
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dc.rights
info:eu-repo/semantics/openAccess
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.subject
ATPASE
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ELECTROPHYSIOLOGY
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PUMP
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SODIUM POTASIUM
dc.subject.classification
Biofísica
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dc.subject.classification
Ciencias Biológicas
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dc.subject.classification
CIENCIAS NATURALES Y EXACTAS
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dc.title
FXYD protein isoforms differentially modulate human Na/K pump function
dc.type
info:eu-repo/semantics/article
dc.type
info:ar-repo/semantics/artículo
dc.type
info:eu-repo/semantics/publishedVersion
dc.date.updated
2021-04-28T21:26:29Z
dc.identifier.eissn
1540-7748
dc.journal.volume
152
dc.journal.number
12
dc.journal.pagination
1-21
dc.journal.pais
Estados Unidos
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dc.description.fil
Fil: Meyer, Dylan J.. Texas Tech University Health Sciences Center; Estados Unidos
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Fil: Bijlani, Sharan. Texas Tech University Health Sciences Center; Estados Unidos
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Fil: de Sautu, Marilina. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Houssay. Instituto de Química y Físico-Química Biológicas "Prof. Alejandro C. Paladini". Universidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Instituto de Química y Físico-Química Biológicas; Argentina
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Fil: Spontarelli, Kerri. Texas Tech University Health Sciences Center; Estados Unidos
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Fil: Young, Victoria C.. Texas Tech University Health Sciences Center; Estados Unidos
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Fil: Gatto, Craig. University of Illinois; Estados Unidos
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Fil: Artigas, Pablo. Texas Tech University Health Sciences Center; Estados Unidos
dc.journal.title
Journal Of General Physiology
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dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1085/jgp.202012660
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://rupress.org/jgp/article-abstract/152/12/e202012660/211559/FXYD-protein-isoforms-differentially-modulate?redirectedFrom=fulltext
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