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与NF2肿瘤抑制基因产物相互作用的细胞蛋白质的检测。

Detection of cellular proteins that interact with the NF2 tumor suppressor gene product.

作者信息

Takeshima H, Izawa I, Lee P S, Safdar N, Levin V A, Saya H

机构信息

Department of Neuro-Onocology, University of Texas M.D. Anderson Cancer Center, Houston 77030.

出版信息

Oncogene. 1994 Aug;9(8):2135-44.

PMID:8035998
Abstract

The neurofibromatosis type 2 (NF2) gene was recently cloned, and the protein it encodes (merlin) was revealed to belong to a family of proteins that link cytoskeletal components with proteins in the cell membrane. To elucidate the biological function of merlin, we produced a bacterial fusion protein consisting of glutathione S-transferase and merlin and used it to detect five merlin-binding cellular proteins, designated p165, p145, p125, p85 and p70, by a protein-binding assay. p165 and merlin were phosphorylated on serine/threonine residues, and immunoprecipitation showed that p85 bound the native form of merlin. Although the entire merlin-ezrin-radixin-moesin (MERM) homology domain of merlin was found to be essential for binding to all five proteins, the MERM homology domains of ezrin and moesin did not bind to any of the five proteins. Since most reported NF2 mutations are in the region we determined was necessary for binding, the mutations probably impair binding. Therefore, the formation of the protein complex is probably crucial for tumor suppression.

摘要

2型神经纤维瘤病(NF2)基因最近被克隆出来,其编码的蛋白质(默林)被发现属于一类将细胞骨架成分与细胞膜中的蛋白质连接起来的蛋白质家族。为了阐明默林的生物学功能,我们制备了一种由谷胱甘肽S-转移酶和默林组成的细菌融合蛋白,并通过蛋白质结合试验用它来检测五种与默林结合的细胞蛋白,分别命名为p165、p145、p125、p85和p70。p165和默林在丝氨酸/苏氨酸残基上被磷酸化,免疫沉淀显示p85与默林的天然形式结合。虽然发现默林的整个默林-埃兹蛋白-根蛋白-膜突蛋白(MERM)同源结构域对于与所有这五种蛋白质的结合至关重要,但埃兹蛋白和膜突蛋白的MERM同源结构域不与这五种蛋白质中的任何一种结合。由于大多数报道的NF2突变都在我们确定的结合所必需的区域,这些突变可能会损害结合。因此,蛋白质复合物的形成可能对肿瘤抑制至关重要。

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