Characterization of the peroxisomal cycling receptor, Pex5p, using a cell-free in vitro import system

被引:75
作者
Gouveia, AM
Guimaraes, CP
Oliveira, ME
Reguenga, C
Sá-Miranda, C
Azevedo, JE
机构
[1] Inst Biol Mol & Celular, P-4150180 Oporto, Portugal
[2] Univ Porto, Inst Ciencias Biomed Abel Salazar, P-4099003 Oporto, Portugal
[3] Inst Genet Med Jacinto Magalhaes, P-4050466 Oporto, Portugal
关键词
D O I
10.1074/jbc.M209498200
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
According to current models of peroxisomal biogenesis, Pex5p cycles between the cytosol and the peroxisome transporting newly synthesized proteins to the organelle matrix. However, little is known regarding the mechanism of this pathway. Here, we show that Pex5p enters and exits the peroxisomal compartment in a process that requires ATP. Insertion of Pex5p into the peroxisomal membrane is blocked by anti-Pex14p IgGs. At the peroxisomal level, two Pex14p-associated populations of Pex5p could be resolved, stage 2 and stage 3 Pex5p, both exposing the majority of their masses into the organelle lumen. Stage 3 Pex5p can be easily detected only under ATP-limiting conditions; in the presence of ATP it leaves the peroxisomal compartment rapidly. Our data suggest that translocation of PTS1-containing proteins across the peroxisomal membrane occurs concomitantly with formation of the Pex5p-Pex14p membrane complex and that this is probably the site from which Pex5p leaves the peroxisomal compartment.
引用
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页码:226 / 232
页数:7
相关论文
共 33 条
[1]   Pex14p, a peroxisomal membrane protein binding both receptors of the two PTS-dependent import pathways [J].
Albertini, M ;
Rehling, P ;
Erdmann, R ;
Girzalsky, W ;
Kiel, JAKW ;
Veenhuis, M ;
Kunau, WH .
CELL, 1997, 89 (01) :83-92
[2]   Pex12p of Saccharomyces cerevisiae is a component of a multi-protein complex essential for peroxisomal matrix protein import [J].
Albertini, M ;
Girzalsky, W ;
Veenhuis, M ;
Kunau, WH .
EUROPEAN JOURNAL OF CELL BIOLOGY, 2001, 80 (04) :257-270
[3]   An isoform of Pex5p, the human PTS1 receptor, is required for the import of PTS2 proteins into peroxisomes [J].
Braverman, N ;
Dodt, G ;
Gould, SJ ;
Valle, D .
HUMAN MOLECULAR GENETICS, 1998, 7 (08) :1195-1205
[4]   The peroxisome biogenesis factors Pex4p, Pex22p, Pex1p, and Pex6p act in the terminal steps of peroxisomal matrix protein import [J].
Collins, CS ;
Kalish, JE ;
Morrell, JC ;
McCaffery, JM ;
Gould, SJ .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (20) :7516-7526
[5]   The human peroxisomal targeting signal receptor, Pex5p, is translocated into the peroxisomal matrix and recycled to the cytosol [J].
Dammai, V ;
Subramani, S .
CELL, 2001, 105 (02) :187-196
[6]   Multiple PEX genes are required for proper subcellular distribution and stability of Pex5p, the PTS1 receptor: Evidence that PTS1 protein import is mediated by a cycling receptor [J].
Dodt, G ;
Gould, SJ .
JOURNAL OF CELL BIOLOGY, 1996, 135 (06) :1763-1774
[7]   MUTATIONS IN THE PTS1 RECEPTOR GENE, PXR1, DEFINE COMPLEMENTATION GROUP-2 OF THE PEROXISOME BIOGENESIS DISORDERS [J].
DODT, G ;
BRAVERMAN, N ;
WONG, C ;
MOSER, A ;
MOSER, HW ;
WATKINS, P ;
VALLE, D ;
GOULD, SJ .
NATURE GENETICS, 1995, 9 (02) :115-125
[8]   The SH3 domain of the Saccharomyces cerevisiae peroxisomal membrane protein Pex13p functions as a docking site for Pex5p, a mobile receptor for the import of PTS1-containing proteins [J].
Elgersma, Y ;
Kwast, L ;
Klein, A ;
VoornBrouwer, T ;
vandenBerg, M ;
Metzig, B ;
America, T ;
Tabak, HF ;
Distel, B .
JOURNAL OF CELL BIOLOGY, 1996, 135 (01) :97-109
[9]   Analysis of the carboxyl-terminal peroxisomal targeting signal 1 in a homologous context in Saccharomyces cerevisiae [J].
Elgersma, Y ;
Vos, A ;
vandenBerg, M ;
vanRoermund, CWT ;
vanderSluijs, P ;
Distel, B ;
Tabak, HF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (42) :26375-26382
[10]   PAS1, A YEAST GENE REQUIRED FOR PEROXISOME BIOGENESIS, ENCODES A MEMBER OF A NOVEL FAMILY OF PUTATIVE ATPASES [J].
ERDMANN, R ;
WIEBEL, FF ;
FLESSAU, A ;
RYTKA, J ;
BEYER, A ;
FROHLICH, KU ;
KUNAU, WH .
CELL, 1991, 64 (03) :499-510