Literature DB >> 7579687

Import of stably folded proteins into peroxisomes.

P A Walton1, P E Hill, S Subramani.   

Abstract

By virtue of their synthesis in the cytoplasm, proteins destined for import into peroxisomes are obliged to traverse the single membrane of this organelle. Because the targeting signal for most peroxisomal matrix proteins is a carboxy-terminal tripeptide sequence (SKL or its variants), these proteins must remain import competent until their translation is complete. We sought to determine whether stably folded proteins were substrates for peroxisomal import. Prefolded proteins stabilized with disulfide bonds and chemical cross-linkers were shown to be substrates for peroxisomal import, as were mature folded and disulfide-bonded IgG molecules containing the peroxisomal targeting signal. In addition, colloidal gold particles conjugated to proteins bearing the peroxisomal targeting signal were translocated into the peroxisomal matrix. These results support the concept that proteins may fold in the mammalian cytosol, before their import into the peroxisome, and that protein unfolding is not a prerequisite for peroxisomal import.

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Year:  1995        PMID: 7579687      PMCID: PMC301228          DOI: 10.1091/mbc.6.6.675

Source DB:  PubMed          Journal:  Mol Biol Cell        ISSN: 1059-1524            Impact factor:   4.138


  29 in total

1.  Large cation-selective pores from rat liver peroxisomal membranes incorporated to planar lipid bilayers.

Authors:  P Labarca; D Wolff; U Soto; C Necochea; F Leighton
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

Review 2.  The mitochondrial protein import apparatus.

Authors:  N Pfanner; W Neupert
Journal:  Annu Rev Biochem       Date:  1990       Impact factor: 23.643

3.  Proton ionophores prevent assembly of a peroxisomal protein.

Authors:  E Bellion; J M Goodman
Journal:  Cell       Date:  1987-01-16       Impact factor: 41.582

Review 4.  Protein import into peroxisomes and biogenesis of the organelle.

Authors:  S Subramani
Journal:  Annu Rev Cell Biol       Date:  1993

5.  Import of firefly luciferase into mammalian peroxisomes in vivo requires nucleoside triphosphates.

Authors:  U Soto; R Pepperkok; W Ansorge; W W Just
Journal:  Exp Cell Res       Date:  1993-03       Impact factor: 3.905

6.  Does aminotriazole inhibit import of catalase into peroxisomes by retarding unfolding?

Authors:  E Middelkoop; A Strijland; J M Tager
Journal:  FEBS Lett       Date:  1991-02-11       Impact factor: 4.124

7.  A 31P NMR study of the internal pH of yeast peroxisomes.

Authors:  K Nicolay; M Veenhuis; A C Douma; W Harder
Journal:  Arch Microbiol       Date:  1987-02       Impact factor: 2.552

8.  Point mutations destabilizing a precursor protein enhance its post-translational import into mitochondria.

Authors:  D Vestweber; G Schatz
Journal:  EMBO J       Date:  1988-04       Impact factor: 11.598

9.  A chimeric mitochondrial precursor protein with internal disulfide bridges blocks import of authentic precursors into mitochondria and allows quantitation of import sites.

Authors:  D Vestweber; G Schatz
Journal:  J Cell Biol       Date:  1988-12       Impact factor: 10.539

10.  Translocation of RNA-coated gold particles through the nuclear pores of oocytes.

Authors:  S I Dworetzky; C M Feldherr
Journal:  J Cell Biol       Date:  1988-03       Impact factor: 10.539

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  77 in total

1.  Visualization of the ER-to-cytosol dislocation reaction of a type I membrane protein.

Authors:  Edda Fiebiger; Craig Story; Hidde L Ploegh; Domenico Tortorella
Journal:  EMBO J       Date:  2002-03-01       Impact factor: 11.598

2.  Peroxisomal catalase in the methylotrophic yeast Candida boidinii: transport efficiency and metabolic significance.

Authors:  H Horiguchi; H Yurimoto; T Goh; T Nakagawa; N Kato; Y Sakai
Journal:  J Bacteriol       Date:  2001-11       Impact factor: 3.490

3.  Interactions of Pex7p and Pex18p/Pex21p with the peroxisomal docking machinery: implications for the first steps in PTS2 protein import.

Authors:  Katharina Stein; Annette Schell-Steven; Ralf Erdmann; Hanspeter Rottensteiner
Journal:  Mol Cell Biol       Date:  2002-09       Impact factor: 4.272

4.  Structural insights into cargo recognition by the yeast PTS1 receptor.

Authors:  Stefanie Hagen; Friedel Drepper; Sven Fischer; Krisztian Fodor; Daniel Passon; Harald W Platta; Michael Zenn; Wolfgang Schliebs; Wolfgang Girzalsky; Matthias Wilmanns; Bettina Warscheid; Ralf Erdmann
Journal:  J Biol Chem       Date:  2015-09-10       Impact factor: 5.157

5.  Saccharomyces cerevisiae pex3p and pex19p are required for proper localization and stability of peroxisomal membrane proteins.

Authors:  E H Hettema; W Girzalsky; M van Den Berg; R Erdmann; B Distel
Journal:  EMBO J       Date:  2000-01-17       Impact factor: 11.598

6.  Poison domains block transit of translocated substrates via the Legionella pneumophila Icm/Dot system.

Authors:  Whitney M Amyot; Dennise deJesus; Ralph R Isberg
Journal:  Infect Immun       Date:  2013-06-24       Impact factor: 3.441

7.  Translocation of a long amino-terminal domain through ER membrane by following signal-anchor sequence.

Authors:  Yuichiro Kida; Katsuyoshi Mihara; Masao Sakaguchi
Journal:  EMBO J       Date:  2005-08-18       Impact factor: 11.598

8.  Pex14/17, a filamentous fungus-specific peroxin, is required for the import of peroxisomal matrix proteins and full virulence of Magnaporthe oryzae.

Authors:  Ling Li; Jiaoyu Wang; Haili Chen; Rongyao Chai; Zhen Zhang; Xueqin Mao; Haiping Qiu; Hua Jiang; Yanli Wang; Guochang Sun
Journal:  Mol Plant Pathol       Date:  2016-12-19       Impact factor: 5.663

9.  Four of the most common mutations in primary hyperoxaluria type 1 unmask the cryptic mitochondrial targeting sequence of alanine:glyoxylate aminotransferase encoded by the polymorphic minor allele.

Authors:  Sonia Fargue; Jackie Lewin; Gill Rumsby; Christopher J Danpure
Journal:  J Biol Chem       Date:  2012-12-10       Impact factor: 5.157

10.  Analysis of the Import of Carboxyl-Terminal Truncations of the 23-Kilodalton Subunit of the Oxygen-Evolving Complex Suggests That Its Structure Is an Important Determinant for Thylakoid Transport.

Authors:  R. A. Roffey; S. M. Theg
Journal:  Plant Physiol       Date:  1996-08       Impact factor: 8.340

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