Departamento de Física, Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires and IFIBA, CONICET, Ciudad Universitaria, Pabellon 1, 1428, Buenos Aires, Argentina.
Institute of Chemistry, University of Campinas, Campinas, SP, 13083-861, Brazil.
J Membr Biol. 2019 Oct;252(4-5):451-464. doi: 10.1007/s00232-019-00088-z. Epub 2019 Aug 22.
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.
间隙连接为相邻细胞之间提供了一种通讯途径。它们由位于各自细胞质膜中的配对连接子组成,其活性可以通过双层组成来调节。在这项工作中,我们研究了嵌入 POPC 脂质双层中的 Cx26 连接子的动态行为,研究了膜蛋白相互作用和离子通过连接子孔的通量。我们分析了不同条件下(有和没有钙离子)的大量原子分子动力学模拟。我们发现脂质-蛋白相互作用主要通过氢键介导。确定了一些特定的氨基酸与 POPC 脂质形成氢键(ARG98、ARG127、ARG165、ARG216、LYS22、LYS221、LYS223、LYS224、SER19、SER131、SER162、SER219、SER222、THR18 和 TYR97、TYR155、TYR212 和 TYR217)。在钙离子存在的情况下,我们发现 HB 寿命存在细微差异。最后,这些 MD 模拟能够识别并解释不同的氯通量通过孔取决于钙离子的存在与否及其在孔内的分布。