Structure and closure of connexin gap junction channels

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• 作者：Atsunori Oshima ; ^{atsu@cespi.nagoya-u.ac.jp" class="auth_mail}
• 关键词：Cx ; connexin ; Vj ; transjunctional voltage ; NT ; amino terminal domain ; CT ; carboxyl terminal domain ; CL ; cytoplasmic loop ; EL ; extracellular loop ; TM ; transmembrane helix ; EM ; electron microscopy ; Cx32*Cx43E1 ; Cx32 chimera in which the EL1 of Cx32 is replaced with the EL1 of Cx43 ; MD ; molecular dynamics
• 刊名：FEBS Letters
• 出版年：17 April, 2014
• 年：2014
• 卷：588
• 期：8
• 页码：1230-1237
• 全文大小：1399 K

文摘

Connexin gap junctions comprise assembled channels penetrating two plasma membranes for which gating regulation is associated with a variety of factors, including voltage, pH, Ca²⁺, and phosphorylation. Functional studies have established that various parts of the connexin peptides are related to channel closure and electrophysiology studies have provided several working models for channel gating. The corresponding structural models supporting these findings, however, are not sufficient because only small numbers of closed connexin structures have been reported. To fully understand the gating mechanisms, the channels should be visualized in both the open and closed states. Electron crystallography and X-ray crystallography studies recently revealed three-dimensional structures of connexin channels in a couple of states in which the main difference is the conformation of the N-terminal domain, which have helped to clarify the structure in regard to channel closure. Here the closure models for connexin gap junction channels inferred from structural and functional studies are described in the context of each domain of the connexin protein associated with gating modulation.