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肌醇磷酸与分离的普列克底物蛋白同源结构域的特异性高亲和力结合。

Specific and high-affinity binding of inositol phosphates to an isolated pleckstrin homology domain.

作者信息

Lemmon M A, Ferguson K M, O'Brien R, Sigler P B, Schlessinger J

机构信息

Department of Pharmacology, New York University Medical Center, New York 10016, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Nov 7;92(23):10472-6. doi: 10.1073/pnas.92.23.10472.

Abstract

Pleckstrin homology (PH) domains are found in many signaling molecules and are thought to be involved in specific intermolecular interactions. Their binding to several proteins and to membranes containing 1-alpha-phosphatidylinositol 4,5-bisphosphate [PtdIns(4,5)P2] has been reported. A region that includes the PH domain has also been implicated in binding of phospholipase C-delta 1 (PLC-delta 1) to both PtdIns(4,5)P2 and D-myo-inositol 1,4,5-trisphosphate [Ins(1,4,5)P3] [Cifuentes, M. E., Delaney, T. & Rebecchi, M. J. (1994) J. Biol. Chem. 269, 1945-1948]. We report herein that the isolated PH domain from PLC-delta 1 binds to both PtdIns(4,5)P2 and Ins(1,4,5)P3 with high affinity and shows the same binding specificity seen by others with whole PLC-delta 1. Thus the PH domain is functionally and structurally modular. These results demonstrate stereo-specific high-affinity binding by an isolated PH domain and further support a functional role for PH domains in the regulation of PLC isoforms. Other PH domains did not bind strongly to the compounds tested, suggesting that inositol phosphates and phospholipids are not likely physiological ligands for all PH domains. Nonetheless, since all PH-domain-containing proteins are associated with membrane surfaces, several PH domains bind to specific sites on membranes, and PH domains appear to be electrostatically polarized, a possible general role for PH domains in membrane association is suggested.

摘要

普列克底物蛋白同源(PH)结构域存在于许多信号分子中,被认为参与特定的分子间相互作用。据报道,它们能与多种蛋白质以及含有1-α-磷脂酰肌醇4,5-二磷酸[PtdIns(4,5)P2]的膜结合。包含PH结构域的一个区域也与磷脂酶C-δ1(PLC-δ1)结合PtdIns(4,5)P2和D-肌醇1,4,5-三磷酸[Ins(1,4,5)P3]有关[西富恩特斯,M.E.,德莱尼,T. & 雷贝奇,M.J.(1994年)《生物化学杂志》269卷,第1945 - 1948页]。我们在此报告,从PLC-δ1分离出的PH结构域能以高亲和力与PtdIns(4,5)P2和Ins(1,4,5)P3结合,并且表现出与其他人用完整PLC-δ1观察到的相同结合特异性。因此,PH结构域在功能和结构上是模块化的。这些结果证明了分离出的PH结构域具有立体特异性高亲和力结合,并进一步支持了PH结构域在调节PLC同工型中的功能作用。其他PH结构域与所测试的化合物结合不强,这表明肌醇磷酸酯和磷脂不太可能是所有PH结构域的生理配体。尽管如此,由于所有含PH结构域的蛋白质都与膜表面相关,一些PH结构域能与膜上的特定位点结合,并且PH结构域似乎是静电极化的,因此提示了PH结构域在膜结合中可能具有普遍作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/bd50/40633/e599df1c93ec/pnas01501-0039-a.jpg

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