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酵母液泡蛋白分选所需的Vps34p是一种具有多种特异性的激酶,它同时具有蛋白激酶和磷脂酰肌醇特异性PI 3激酶活性。

Vps34p required for yeast vacuolar protein sorting is a multiple specificity kinase that exhibits both protein kinase and phosphatidylinositol-specific PI 3-kinase activities.

作者信息

Stack J H, Emr S D

机构信息

Division of Cellular and Molecular Medicine, Howard Hughes Medical Institute, University of California, San Diego School of Medicine, La Jolla 92093-0668.

出版信息

J Biol Chem. 1994 Dec 16;269(50):31552-62.

PMID:7989323
Abstract

The Vps15 protein kinase and the Vps34 phosphatidylinositol 3-kinase have been shown to function as a membrane-associated complex which facilitates the delivery of proteins to the vacuole in yeast. Biochemical characterization of the autophosphorylation reaction catalyzed by Vps15p demonstrates that it is a functional serine/threonine protein kinase. In addition, we show that the Vps34 phosphatidylinositol 3-kinase undergoes an autophosphorylation event both in vivo and in vitro, indicating that it represents a novel multiple specificity kinase capable of phosphorylating both protein and lipid substrates. Vps34p is phosphorylated predominately on serine in vivo and is able to phosphorylate serine, threonine, and tyrosine residues in vitro. Mutant Vps34 proteins containing alterations in conserved amino acids in the lipid kinase domain are severely defective for both PI 3-kinase activity and autophosphorylation. Characterization of the PI 3-kinase activity of Vps34p demonstrates that it, unlike the mammalian p110 PI 3-kinase, is highly resistant to the PI 3-kinase inhibitors wortmannin and LY294002. We also find that Vps34p is a phosphatidylinositol-specific 3-kinase, as it is able to utilize phosphatidylinositol (PtdIns) but not PtdIns(4)P or PtdIns(4,5)P2 as substrates in an in vitro PI kinase reaction. The substrate specificity, wortmannin resistance, and other biochemical characteristics of its PtdIns 3-kinase activity suggest that Vps34p is quite similar to a PtdIns-specific 3-kinase activity recently characterized from mammalian cells. These data indicate the existence of a family of PI 3-kinases composed of p110-like PI 3-kinases and Vps34p-like PtdIns-specific 3-kinases. On the basis of the role for Vps34p in vacuolar protein sorting, we propose that the production of a specific phosphoinositide, PtdIns(3)P, is involved in regulating intracellular protein sorting reactions in eukaryotic cells.

摘要

Vps15蛋白激酶和Vps34磷脂酰肌醇3激酶已被证明作为一种膜相关复合物发挥作用,该复合物促进蛋白质在酵母中向液泡的运输。对Vps15p催化的自磷酸化反应的生化特性分析表明,它是一种功能性丝氨酸/苏氨酸蛋白激酶。此外,我们发现Vps34磷脂酰肌醇3激酶在体内和体外都会发生自磷酸化事件,这表明它是一种新型的多特异性激酶,能够磷酸化蛋白质和脂质底物。Vps34p在体内主要在丝氨酸上被磷酸化,并且在体外能够磷酸化丝氨酸、苏氨酸和酪氨酸残基。脂质激酶结构域中保守氨基酸发生改变的突变型Vps34蛋白在PI 3激酶活性和自磷酸化方面都存在严重缺陷。对Vps34p的PI 3激酶活性的特性分析表明,与哺乳动物p110 PI 3激酶不同,它对PI 3激酶抑制剂渥曼青霉素和LY294002具有高度抗性。我们还发现Vps34p是一种磷脂酰肌醇特异性3激酶,因为在体外PI激酶反应中它能够利用磷脂酰肌醇(PtdIns)作为底物,而不能利用磷脂酰肌醇-4-磷酸(PtdIns(4)P)或磷脂酰肌醇-4,5-二磷酸(PtdIns(4,5)P2)。其PtdIns 3激酶活性的底物特异性、对渥曼青霉素的抗性以及其他生化特性表明,Vps34p与最近在哺乳动物细胞中鉴定出的一种磷脂酰肌醇特异性3激酶活性非常相似。这些数据表明存在一个由p110样PI 3激酶和Vps34p样磷脂酰肌醇特异性3激酶组成的PI 3激酶家族。基于Vps34p在液泡蛋白分选中的作用,我们提出一种特定的磷酸肌醇磷脂酰肌醇-3-磷酸(PtdIns(3)P)的产生参与调节真核细胞中的细胞内蛋白分选反应。

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