Hansenula polymorpha Pex3p is a peripheral component of the peroxisomal membrane.

被引:22
作者
Haan, GJ [1 ]
Faber, KN [1 ]
Baerends, RJS [1 ]
Koek, A [1 ]
Krikken, A [1 ]
Kiel, JAKW [1 ]
van der Klei, IJ [1 ]
Veenhuis, M [1 ]
机构
[1] Univ Groningen, Groningen Biomol Sci & Biotech Inst, NL-9750 AA Haren, Netherlands
关键词
D O I
10.1074/jbc.M108569200
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
Hansenula polymorpha Pex3p plays an essential role in the biogenesis and maintenance of the peroxisomal membrane. In the initial report, bakers' yeast Pex3p was suggested to represent an integral component of the peroxisomal membrane, containing one membrane-spanning region that exposes the N terminus of the protein into the organellar matrix. Biochemically, HpPex3p behaved like an integral membrane protein as it was resistant toward high salt and carbonate treatment. However, urea fully removed Pex3p from the membrane under conditions in which the integral membrane protein Pex10p was resistant to this treatment. Additional experiments, including protease protection assays and pre-embedding labeling experiments on purified organellar fractions from cells that produced Pex3ps carrying Myc epitopes at various selected locations in the protein, revealed that invariably all Myc tags were accessible for externally added proteases and antibodies, independent of the presence of detergents. Also, overproduction of Pex3p failed to demonstrate the typical integral membrane protein structures in fracture faces of freeze-fractured peroxisomes. Taken together, our data suggest that HpPex3p does not span the peroxisomal membrane but instead is tightly associated to the cytosolic face of the organelle where it may be present in focal protein clusters.
引用
收藏
页码:26609 / 26617
页数:9
相关论文
共 48 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]  
ARGOS P, 1982, EUR J BIOCHEM, V128, P565
[3]  
Baerends RJS, 1997, YEAST, V13, P1437
[4]   A stretch of positively charged amino acids at the N terminus of Hansenula polymorpha Pex3p is involved in incorporation of the protein into the peroxisomal membrane [J].
Baerends, RJS ;
Faber, KN ;
Kram, AM ;
Kiel, JAKW ;
van der Klei, IJ ;
Veenhuis, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (14) :9986-9995
[5]   The Hansenula polymorpha PER9 gene encodes a peroxisomal membrane protein essential for peroxisome assembly and integrity [J].
Baerends, RJS ;
Rasmussen, SW ;
Hilbrands, RE ;
vanderHeide, M ;
Faber, KN ;
Reuvekamp, PTW ;
Kiel, JAKW ;
Cregg, JM ;
vanderKlei, IJ ;
Veenhuis, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (15) :8887-8894
[6]   The sorting sequence of the peroxisomal integral membrane protein PMP47 is contained within a short hydrophilic loop [J].
Dyer, JM ;
McNew, JA ;
Goodman, JM .
JOURNAL OF CELL BIOLOGY, 1996, 133 (02) :269-280
[7]   ANALYSIS OF MEMBRANE AND SURFACE PROTEIN SEQUENCES WITH THE HYDROPHOBIC MOMENT PLOT [J].
EISENBERG, D ;
SCHWARZ, E ;
KOMAROMY, M ;
WALL, R .
JOURNAL OF MOLECULAR BIOLOGY, 1984, 179 (01) :125-142
[8]   Overexpression of Pex15p, a phosphorylated peroxisomal integral membrane protein required for peroxisome assembly in S-cerevisiae, causes proliferation of the endoplasmic reticulum membrane [J].
Elgersma, Y ;
Kwast, L ;
van den Berg, M ;
Snyder, WB ;
Distel, B ;
Subramani, S ;
Tabak, HF .
EMBO JOURNAL, 1997, 16 (24) :7326-7341
[9]   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
[10]   Structural analysis of cloned plasma membrane proteins by freeze-fracture electron microscopy [J].
Eskandari, S ;
Wright, EM ;
Kreman, M ;
Starace, DM ;
Zampighi, GA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (19) :11235-11240