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一种酵母蛋白激酶的分离,该激酶被SRP1(Srp1p)编码的蛋白激活,并使与核定位信号肽复合的Srp1p磷酸化。

Isolation of a yeast protein kinase that is activated by the protein encoded by SRP1 (Srp1p) and phosphorylates Srp1p complexed with nuclear localization signal peptides.

作者信息

Azuma Y, Tabb M M, Vu L, Nomura M

机构信息

Department of Biological Chemistry, University of California, Irvine 92717, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 May 23;92(11):5159-63. doi: 10.1073/pnas.92.11.5159.

Abstract

Srp1p, the protein encoded by SRP1 of Saccharomyces cerevisiae, is a nuclear-pore-associated protein. Its Xenopus homolog, importin, was recently shown to be an essential component required for nuclear localization signal (NLS)-dependent binding of karyophilic proteins to the nuclear envelope [Gorlich, D., Prehn, S., Laskey, R. A. & Hartman, E. (1994) Cell 79, 767-778]. We have discovered a protein kinase whose activity is stimulated by Srp1p (Srp1p fused to glutathione S-transferase and expressed in Escherichia coli) and is detected by phosphorylation of Srp1p and of a 36-kDa protein, a component of the protein kinase complex. The enzyme, called Srp1p kinase, is a protein-serine kinase and was found in extracts in two related complexes of approximately 180 kDa and 220 kDa. The second complex, when purified, contained four protein components including the 36-kDa protein. We observed that, upon purification of the kinase, phosphorylation of Srp1p became very weak, while activation of phosphorylation of the 36-kDa protein by Srp1p remained unaltered. Significantly, NLS peptides and the nuclear proteins we have tested greatly stimulated phosphorylation of Srp1p, suggesting that Srp1p, complexed with karyophilic proteins carrying an NLS, is the in vivo substrate of this protein kinase.

摘要

Srp1p是酿酒酵母SRP1编码的蛋白质,是一种与核孔相关的蛋白质。其非洲爪蟾同源物输入蛋白最近被证明是核定位信号(NLS)依赖的亲核蛋白与核膜结合所需的必需成分[戈利希,D.,普雷恩,S.,拉斯基,R.A.和哈特曼,E.(1994年)《细胞》79卷,767 - 778页]。我们发现了一种蛋白激酶,其活性受Srp1p(与谷胱甘肽S - 转移酶融合并在大肠杆菌中表达的Srp1p)刺激,并通过Srp1p和一种36 kDa蛋白质(蛋白激酶复合物的一个成分)的磷酸化来检测。这种酶被称为Srp1p激酶,是一种蛋白丝氨酸激酶,在提取物中以大约180 kDa和220 kDa的两种相关复合物形式存在。第二种复合物纯化后包含四个蛋白质成分,包括36 kDa蛋白质。我们观察到,在激酶纯化后,Srp1p的磷酸化变得非常弱,而Srp1p对36 kDa蛋白质磷酸化的激活保持不变。重要的是,我们测试的NLS肽和核蛋白极大地刺激了Srp1p的磷酸化,这表明与携带NLS的亲核蛋白复合的Srp1p是这种蛋白激酶在体内的底物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7247/41868/6d85a2e0011e/pnas01487-0449-a.jpg

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