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首页> 外文期刊>Cellular Signalling >G-protein alpha subunit interaction and guanine nucleotide dissociation inhibitor activity of the dual GoLoco motif protein PCP-2 (Purkinje cell protein-2)
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G-protein alpha subunit interaction and guanine nucleotide dissociation inhibitor activity of the dual GoLoco motif protein PCP-2 (Purkinje cell protein-2)

机译:双重GoLoco基序蛋白PCP-2(Purkinje细胞蛋白2)的G蛋白α亚基相互作用和鸟嘌呤核苷酸解离抑制剂活性

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摘要

Purkinje cell protein-2 (PCP-2; L7/GPSM4) is a GoLoco motif-containing protein that is specifically expressed in Purkinje and retinal ON bipolar cells. An alternative splice variant of PCP-2 has recently been isolated which contains two GoLoco motifs. Although the second GoLoco motif (GL2) of PCP-2 has been reported to interact with G alpha-subunits, a complete biochemical analysis of each individual motif of PCP-2 has not been performed. We demonstrate that the first GoLoco motif (GL1) of PCP-2 is equipotent as a guanine nucleotide dissociation inhibitor (GDI) towards G alpha(i1) and G alpha(i2), while it has sevenfold lower GDI activity for G alpha(13) and greater than 20-fold lower GDI activity against Got.. In contrast we found PCP-2 GL2 to be essentially equipotent as a GDI for all G alpha(i) subunits, but it had negligible activity toward Get.. Using coimmunoprecipitation from COS-7 cells, we found that PCP-2 was only able to interact with Gai I but not Get. nor G alpha-subunits from other families (G alpha(s), G alpha(q), or G alpha(12)) Mutational analysis of a non-canonical residue (glycine 24) in human PCP-2 GL1 provided evidence for heterogeneity in mechanisms of Gai interactions with GoLoco motifs. Collectively, the data demonstrate that PCP-2 is a comparatively weak GoLoco motif protein that exhibits highest affinity interactions and GDI activity toward G alpha(i1), G alpha(i2), and G alpha(i3) subunits. (c) 2005 Elsevier Inc. All rights reserved.
机译:浦肯野细胞蛋白2(PCP-2; L7 / GPSM4)是一种含有GoLoco基序的蛋白,在浦肯野和视网膜ON双极细胞中特异性表达。最近分离出了包含两个GoLoco基序的PCP-2的另一个剪接变体。尽管已经报道了PCP-2的第二个GoLoco基序(GL2)与Gα亚基相互作用,但尚未对PCP-2的每个基序进行完整的生化分析。我们证明了PCP-2的第一个GoLoco基序(GL1)是作为鸟嘌呤核苷酸解离抑制剂(GDI)朝着G alpha(i1)和G alpha(i2)等价的,而它对G alpha(13)的GDI活性却降低了七倍),并且对Got的GDI活性降低了20倍以上。相反,我们发现PCP-2 GL2与所有G alpha(i)亚基的GDI本质上均等,但对Get的活性却微不足道。在COS-7细胞中,我们发现PCP-2仅能与Gai I相互作用,而不能与Geti相互作用。或来自其他家族的G alpha亚基(G alpha,G alpha(q)或G alpha(12))对人PCP-2 GL1中非规范残基(甘氨酸24)的突变分析提供了异质性证据与GoLoco主题的Gai交互作用机制有关。总体而言,数据表明PCP-2是一种相对较弱的GoLoco基序蛋白,对G alpha(i1),G alpha(i2)和G alpha(i3)亚基表现出最高的亲和力和GDI活性。 (c)2005 Elsevier Inc.保留所有权利。

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