The PX domain as a novel phosphoinositide-binding module

被引:85
作者
Ago, T
Takeya, R
Hiroaki, H
Kuribayashi, F
Ito, T
Kohda, D
Sumimoto, H
机构
[1] Kyushu Univ, Med Inst Bioregulat, Higashi Ku, Fukuoka 8128582, Japan
[2] Kyushu Univ, Grad Sch Med Sci, Dept Biol Mol & Struct, Fukuoka 8128582, Japan
[3] Biomol Engn Res Inst, Dept Biol Struct, Suita, Osaka 5650874, Japan
[4] Kanazawa Univ, Canc Res Inst, Div Genome Biol, Kanazawa, Ishikawa 9200934, Japan
关键词
PX domain; NADPH oxidase; p40(phox); p47(phox); Bem1p; phosphoinositide; membrane localization; membrane trafficking; sorting nexin 3; Vam7p;
D O I
10.1006/bbrc.2001.5629
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The phox (phagocyte oxidase) homology (PX) domain occurs in the mammalian phox proteins p40(phox) and p47(phox). the polarity establishment protein Bem1p in budding yeast, and a variety of proteins involved in membrane trafficking. Here we show that the PX domains of p40(phox) and p47(phox) directly bind to phosphoinositides: P40(phox) prefers Ptdlns(3)P, while p47(phox) does Ptdlns(4)P and Ptdlns(3,4)P-2. In addition, the Bem1p PX domain also interacts with Ptdlns(4)P. When the P40(phox) PX domain is expressed as a fusion to green fluorescent protein in HeLa cells, it exists at early endosomes where Ptdlns(3)P is enriched. Furthermore, a mutant P40(phox) PX carrying the substitution of Lys for Arg105 only weakly binds to phosphoinositides in vitro, and fails to locate to early endosomes. Thus the PX domain functions as a novel phosphoinositide-binding module and likely participates in targeting of proteins to membranes. (C) 2001 Academic Press.
引用
收藏
页码:733 / 738
页数:6
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