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FYVE结构域蛋白作为磷脂酰肌醇3-磷酸的效应分子

FYVE finger proteins as effectors of phosphatidylinositol 3-phosphate.

作者信息

Gaullier J M, Simonsen A, D'Arrigo A, Bremnes B, Stenmark H

机构信息

Department of Biochemistry, Norwegian Radium Hospital, Oslo, Norway.

出版信息

Chem Phys Lipids. 1999 Apr;98(1-2):87-94. doi: 10.1016/s0009-3084(99)00021-3.

Abstract

Phosphatidylinositol 3-phosphate (PtdIns(3)P), generated via the phosphorylation of phosphatidylinositol by phosphatidylinositol 3-kinase (PI 3-kinase), plays an essential role in intracellular membrane traffic. The underlying mechanism is still not understood in detail, but the recent identification of the FYVE finger as a protein domain that binds specifically to PtdIns(3)P provides a number of potential effectors for PtdIns(3)P. The FYVE finger (named after the first letter of the four proteins containing it; Fab1p, YOTB, Vac1p and EEA1) is a double-zinc binding domain that is conserved in more than 30 proteins from yeast to mammals. It is found in several proteins involved in intracellular traffic, and FYVE finger mutations that affect zinc binding are associated with the loss of function of several of these proteins. The interaction of FYVE fingers with PtdIns(3)P may serve three alternative functions: First, to recruit cytosolic FYVE finger proteins to PtdIns(3)P-containing membranes (in concert with accessory molecules); second, to enrich for membrane bound FYVE finger proteins into PtdIns(3)P containing microdomains within the membrane; and third, to modulate the activity of membrane bound FYVE finger proteins.

摘要

磷脂酰肌醇3-磷酸(PtdIns(3)P)由磷脂酰肌醇3-激酶(PI 3-激酶)催化磷脂酰肌醇磷酸化产生,在细胞内膜运输中起重要作用。其潜在机制仍未完全清楚,但最近发现的FYVE结构域是一种能特异性结合PtdIns(3)P的蛋白质结构域,这为PtdIns(3)P提供了许多潜在的效应分子。FYVE结构域(以包含它的四种蛋白质的首字母命名:Fab1p、YOTB、Vac1p和EEA1)是一种双锌结合结构域,在从酵母到哺乳动物的30多种蛋白质中保守。它存在于几种参与细胞内运输的蛋白质中,影响锌结合的FYVE结构域突变与其中几种蛋白质的功能丧失有关。FYVE结构域与PtdIns(3)P的相互作用可能具有三种不同功能:第一,将胞质中的FYVE结构域蛋白募集到含有PtdIns(3)P的膜上(与辅助分子协同作用);第二,使膜结合的FYVE结构域蛋白富集到膜内含有PtdIns(3)P的微结构域中;第三,调节膜结合的FYVE结构域蛋白的活性。

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