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
相关论文
共 26 条
[11]   A sorting nexin-1 homologue, vps5p, forms a complex with vps17p and is required for recycling the vacuolar protein-sorting receptor [J].
Horazdovsky, BF ;
Davies, BA ;
Seaman, MNJ ;
McLaughlin, SA ;
Yoon, S ;
Emr, SD .
MOLECULAR BIOLOGY OF THE CELL, 1997, 8 (08) :1529-1541
[12]   Novel modular domain PB1 recognizes PC motif to mediate functional protein-protein interactions [J].
Ito, T ;
Matsui, Y ;
Ago, T ;
Ota, K ;
Sumimoto, H .
EMBO JOURNAL, 2001, 20 (15) :3938-3946
[13]   The PX domains of p47phox and p40phox bind to lipid products of Pl(3)K [J].
Kanai, F ;
Liu, H ;
Field, SJ ;
Akbary, H ;
Matsuo, T ;
Brown, GE ;
Cantley, LC ;
Yaffe, MB .
NATURE CELL BIOLOGY, 2001, 3 (07) :675-678
[14]   Functional modules and expression of mouse p40phox and p67phox, SH3-domain-containing proteins -: Involved in the phagocyte NADPH oxidase complex [J].
Mizuki, K ;
Kadomatsu, K ;
Hata, K ;
Ito, T ;
Fan, QW ;
Kage, Y ;
Fukumaki, Y ;
Sakaki, Y ;
Takeshige, K ;
Sumimoto, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 251 (03) :573-582
[15]   The PC motif:: a novel and evolutionarily conserved sequence involved in interaction between p40phox and p67phox, SH3 domain-containing cytosolic factors of the phagocyte NADPH oxidase [J].
Nakamura, R ;
Sumimoto, H ;
Mizuki, K ;
Hata, K ;
Ago, T ;
Kitajima, S ;
Takeshige, K ;
Sakaki, Y ;
Ito, T .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1998, 251 (03) :583-589
[16]   Human homologues of the Caenorhabditis elegans cell polarity protein PAR6 as an adaptor that links the small GTPases Rac and Cdc42 to atypical protein kinase C [J].
Noda, Y ;
Takeya, R ;
Ohno, S ;
Naito, S ;
Ito, T ;
Sumimoto, H .
GENES TO CELLS, 2001, 6 (02) :107-119
[17]   Identification of an early endosomal protein regulated by phosphatidylinositol 3-kinase [J].
Patki, V ;
Virbasius, J ;
Lane, WS ;
Toh, BH ;
Shpetner, HS ;
Corvera, S .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (14) :7326-7330
[18]   Novel domains in NADPH oxidase subunits, sorting nexins, and PtdIns 3-kinases: Binding partners of SH3 domains? [J].
Ponting, CP .
PROTEIN SCIENCE, 1996, 5 (11) :2353-2357
[19]  
Roos D, 1996, BLOOD, V87, P1663
[20]   Vam7p, a SNAP-25-like molecule, and Vam3p, a syntaxin homolog, function together in yeast vacuolar protein trafficking [J].
Sato, TK ;
Darsow, T ;
Emr, SD .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (09) :5308-5319