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PDZ蛋白对G蛋白偶联受体转运及信号通路的调控

PDZ Protein Regulation of G Protein-Coupled Receptor Trafficking and Signaling Pathways.

作者信息

Dunn Henry A, Ferguson Stephen S G

机构信息

J. Allyn Taylor Centre for Cell Biology, Robarts Research Institute, and the Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada.

J. Allyn Taylor Centre for Cell Biology, Robarts Research Institute, and the Department of Physiology and Pharmacology, University of Western Ontario, London, Ontario, Canada

出版信息

Mol Pharmacol. 2015 Oct;88(4):624-39. doi: 10.1124/mol.115.098509. Epub 2015 Mar 25.

Abstract

G protein-coupled receptors (GPCRs) contribute to the regulation of every aspect of human physiology and are therapeutic targets for the treatment of numerous diseases. As a consequence, understanding the myriad of mechanisms controlling GPCR signaling and trafficking is essential for the development of new pharmacological strategies for the treatment of human pathologies. Of the many GPCR-interacting proteins, postsynaptic density protein of 95 kilodaltons, disc large, zona occludens-1 (PDZ) domain-containing proteins appear most abundant and have similarly been implicated in disease mechanisms. PDZ proteins play an important role in regulating receptor and channel protein localization within synapses and tight junctions and function to scaffold intracellular signaling protein complexes. In the current study, we review the known functional interactions between PDZ domain-containing proteins and GPCRs and provide insight into the potential mechanisms of action. These PDZ domain-containing proteins include the membrane-associated guanylate-like kinases [postsynaptic density protein of 95 kilodaltons; synapse-associated protein of 97 kilodaltons; postsynaptic density protein of 93 kilodaltons; synapse-associated protein of 102 kilodaltons; discs, large homolog 5; caspase activation and recruitment domain and membrane-associated guanylate-like kinase domain-containing protein 3; membrane protein, palmitoylated 3; calcium/calmodulin-dependent serine protein kinase; membrane-associated guanylate kinase protein (MAGI)-1, MAGI-2, and MAGI-3], Na(+)/H(+) exchanger regulatory factor proteins (NHERFs) (NHERF1, NHERF2, PDZ domain-containing kidney protein 1, and PDZ domain-containing kidney protein 2), Golgi-associated PDZ proteins (Gα-binding protein interacting protein, C-terminus and CFTR-associated ligand), PDZ domain-containing guanine nucleotide exchange factors (GEFs) 1 and 2, regulator of G protein signaling (RGS)-homology-RhoGEFs (PDZ domain-containing RhoGEF and leukemia-associated RhoGEF), RGS3 and RGS12, spinophilin and neurabin-1, SRC homology 3 domain and multiple ankyrin repeat domain (Shank) proteins (Shank1, Shank2, and Shank3), partitioning defective proteins 3 and 6, multiple PDZ protein 1, Tamalin, neuronal nitric oxide synthase, syntrophins, protein interacting with protein kinase C α 1, syntenin-1, and sorting nexin 27.

摘要

G蛋白偶联受体(GPCRs)参与调节人体生理的各个方面,是治疗多种疾病的靶点。因此,了解控制GPCR信号传导和运输的众多机制对于开发治疗人类疾病的新药理学策略至关重要。在众多与GPCR相互作用的蛋白质中,含95千道尔顿突触后致密蛋白、盘状大蛋白、紧密连接蛋白1(PDZ)结构域的蛋白质似乎最为丰富,并且同样与疾病机制有关。PDZ蛋白在调节突触和紧密连接内的受体和通道蛋白定位以及构建细胞内信号蛋白复合物的功能方面发挥着重要作用。在本研究中,我们回顾了含PDZ结构域的蛋白质与GPCR之间已知的功能相互作用,并深入探讨了潜在的作用机制。这些含PDZ结构域的蛋白质包括膜相关鸟苷酸样激酶[95千道尔顿突触后致密蛋白;97千道尔顿突触相关蛋白;93千道尔顿突触后致密蛋白;102千道尔顿突触相关蛋白;盘状大同源物5;半胱天冬酶激活和募集结构域及含膜相关鸟苷酸样激酶结构域蛋白3;膜蛋白,棕榈酰化3;钙/钙调蛋白依赖性丝氨酸蛋白激酶;膜相关鸟苷酸激酶蛋白(MAGI)-1、MAGI-2和MAGI-3]、钠/氢交换调节因子蛋白(NHERFs)(NHERF1、NHERF2、含PDZ结构域的肾蛋白1和含PDZ结构域的肾蛋白2)、高尔基体相关PDZ蛋白(Gα结合蛋白相互作用蛋白、C末端和CFTR相关配体)、含PDZ结构域的鸟嘌呤核苷酸交换因子(GEFs)1和2、G蛋白信号调节剂(RGS)-同源-RhoGEFs(含PDZ结构域的RhoGEF和白血病相关RhoGEF)、RGS3和RGS12、亲嗜素和神经肌动蛋白-1、SRC同源3结构域和多个锚蛋白重复结构域(Shank)蛋白(Shank1、Shank2和Shank3)、分隔缺陷蛋白3和6、多个PDZ蛋白1、塔马林、神经元型一氧化氮合酶、肌萎缩蛋白、与蛋白激酶Cα1相互作用的蛋白、syntenin-1和分选衔接蛋白27。

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