共 33 条
Characterization of the peroxisomal cycling receptor, Pex5p, using a cell-free in vitro import system
被引:75
作者:

Gouveia, AM
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机构: Inst Biol Mol & Celular, P-4150180 Oporto, Portugal

Guimaraes, CP
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机构: Inst Biol Mol & Celular, P-4150180 Oporto, Portugal

Oliveira, ME
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机构: Inst Biol Mol & Celular, P-4150180 Oporto, Portugal

Reguenga, C
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h-index: 0
机构: Inst Biol Mol & Celular, P-4150180 Oporto, Portugal

Sá-Miranda, C
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机构: Inst Biol Mol & Celular, P-4150180 Oporto, Portugal

Azevedo, JE
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机构: Inst Biol Mol & Celular, P-4150180 Oporto, Portugal
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.
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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

Albertini, M
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY

Rehling, P
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY

Erdmann, R
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY

Girzalsky, W
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY

Kiel, JAKW
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY

Veenhuis, M
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY

Kunau, WH
论文数: 0 引用数: 0
h-index: 0
机构: RUHR UNIV BOCHUM,ABT ZELLBIOCHEM,D-44780 BOCHUM,GERMANY
[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

Albertini, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Electron Microscopy Lab, Haren, Netherlands

Girzalsky, W
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Electron Microscopy Lab, Haren, Netherlands

Veenhuis, M
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Electron Microscopy Lab, Haren, Netherlands

Kunau, WH
论文数: 0 引用数: 0
h-index: 0
机构: Univ Groningen, Electron Microscopy Lab, Haren, Netherlands
[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

Braverman, N
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA

Dodt, G
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA

Gould, SJ
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA

Valle, D
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
[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

Collins, CS
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA

Kalish, JE
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA

Morrell, JC
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA

McCaffery, JM
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA

Gould, SJ
论文数: 0 引用数: 0
h-index: 0
机构: Johns Hopkins Univ, Sch Med, Dept Biol Chem, Baltimore, MD 21205 USA
[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

Dammai, V
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Div Biol, Mol Biol Sect, La Jolla, CA 92093 USA Univ Calif San Diego, Div Biol, Mol Biol Sect, La Jolla, CA 92093 USA

Subramani, S
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Calif San Diego, Div Biol, Mol Biol Sect, La Jolla, CA 92093 USA Univ Calif San Diego, Div Biol, Mol Biol Sect, La Jolla, CA 92093 USA
[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

Dodt, G
论文数: 0 引用数: 0
h-index: 0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT BIOL CHEM,BALTIMORE,MD 21205 JOHNS HOPKINS UNIV,SCH MED,DEPT BIOL CHEM,BALTIMORE,MD 21205

Gould, SJ
论文数: 0 引用数: 0
h-index: 0
机构:
JOHNS HOPKINS UNIV,SCH MED,DEPT BIOL CHEM,BALTIMORE,MD 21205 JOHNS HOPKINS UNIV,SCH MED,DEPT BIOL CHEM,BALTIMORE,MD 21205
[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

DODT, G
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

BRAVERMAN, N
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

WONG, C
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

MOSER, A
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

MOSER, HW
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

WATKINS, P
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

VALLE, D
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205

GOULD, SJ
论文数: 0 引用数: 0
h-index: 0
机构: JOHNS HOPKINS UNIV HOSP,SCH MED,KENNEDY KRIEGER RES INST,BALTIMORE,MD 21205
[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

Elgersma, Y
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

Kwast, L
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

Klein, A
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

VoornBrouwer, T
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

vandenBerg, M
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

Metzig, B
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

America, T
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

Tabak, HF
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS

Distel, B
论文数: 0 引用数: 0
h-index: 0
机构:
UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS UNIV AMSTERDAM, ACAD MED CTR, DEPT BIOCHEM, NL-1105 AZ AMSTERDAM, NETHERLANDS
[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

Elgersma, Y
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS

Vos, A
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS

vandenBerg, M
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS

vanRoermund, CWT
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS

vanderSluijs, P
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS

Distel, B
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS

Tabak, HF
论文数: 0 引用数: 0
h-index: 0
机构: UNIV AMSTERDAM,ACAD MED CTR,DEPT BIOCHEM,NL-1105 AZ AMSTERDAM,NETHERLANDS
[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

ERDMANN, R
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum

WIEBEL, FF
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum

FLESSAU, A
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum

RYTKA, J
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum

BEYER, A
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum

FROHLICH, KU
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum

KUNAU, WH
论文数: 0 引用数: 0
h-index: 0
机构: Abteilung fur Zellbiochemie Institut fur Physiologische Chemie Ruhr-Universität Bochum