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The Effects of Calcium on Lipid-Protein Interactions and Ion Flux in the Cx26 Connexon Embedded into a POPC Bilayer.
Albano, Juan M R; Jara, Gabriel E; Fernández, M Laura; Facelli, Julio C; Ferraro, Marta B; Pickholz, Monica.
  • Albano JMR; Departamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires and IFIBA, CONICET, Ciudad Universitaria, Pabellon 1, 1428, Buenos Aires, Argentina.
  • Jara GE; Institute of Chemistry, University of Campinas, Campinas, SP, 13083-861, Brazil.
  • Fernández ML; Departamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Facelli JC; Instituto de Física del Plasma (INFIP), CONICET- Universidad de Buenos Aires, Buenos Aires, Argentina.
  • Ferraro MB; Department of Biomedical Informatics and Center for Clinical and Translational Research, The University of Utah, 421 Wakara Way, Suite 140, Salt Lake City, UT, 84108, USA.
  • Pickholz M; Departamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires and IFIBA, CONICET, Ciudad Universitaria, Pabellon 1, 1428, Buenos Aires, Argentina.
J Membr Biol ; 252(4-5): 451-464, 2019 10.
Article en En | MEDLINE | ID: mdl-31440780
ABSTRACT
Gap junctions provide a communication pathway between adjacent cells. They are formed by paired connexons that reside in the plasma membrane of their respective cell and their activity can be modulated by the bilayer composition. In this work, we study the dynamic behavior of a Cx26 connexon embedded in a POPC lipid bilayer, studying the membrane protein interactions and the ion flux though the connexon pore. We analyzed extensive atomistic molecular dynamics simulations for different conditions, with and without calcium ions. We found that lipid-protein interactions were mainly mediated by hydrogen bonds. Specific amino acids were identified forming hydrogen bonds with the POPC lipids (ARG98, ARG127, ARG165, ARG216, LYS22, LYS221, LYS223, LYS224, SER19, SER131, SER162, SER219, SER222, THR18 and TYR97, TYR155, TYR212, and TYR217). In the presence of calcium ions, we found subtle differences on the HB lifetimes. Finally, these MD simulations are able to identify and explain differential chlorine flux through the pore depending on the presence or absence of the calcium ions and its distribution within the pore.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfatidilcolinas / Calcio / Conexinas / Simulación de Dinámica Molecular / Membrana Dobles de Lípidos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Fosfatidilcolinas / Calcio / Conexinas / Simulación de Dinámica Molecular / Membrana Dobles de Lípidos Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Año: 2019 Tipo del documento: Article