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P2X嘌呤能受体的组装与运输(综述)

Assembly and trafficking of P2X purinergic receptors (Review).

作者信息

Murrell-Lagnado Ruth D, Qureshi Omar S

机构信息

Department of Pharmacology, University of Cambridge, UK.

出版信息

Mol Membr Biol. 2008 May;25(4):321-31. doi: 10.1080/09687680802050385.

Abstract

P2X receptors are cation selective ion channels gated by the binding of extracellular ATP. Seven subtypes have been identified and they have widespread and overlapping distributions throughout the body. They form homo- and heterotrimeric complexes that differ in their functional properties and subcellular localization. They form part of larger signalling complexes, interacting with unrelated ion channels and other membrane and cytosolic proteins. Up- or down-regulation of their expression is associated with several disease states. This review aims to summarize recent work on the assembly and trafficking of this family of receptors.

摘要

P2X受体是由细胞外ATP结合而门控的阳离子选择性离子通道。已鉴定出七种亚型,它们在全身具有广泛且重叠的分布。它们形成同三聚体和异三聚体复合物,其功能特性和亚细胞定位各不相同。它们构成更大信号复合物的一部分,与不相关的离子通道以及其他膜蛋白和胞质蛋白相互作用。其表达的上调或下调与多种疾病状态相关。本综述旨在总结关于该受体家族组装和运输的最新研究工作。

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