Literature DB >> 10511706

How to get a folded protein across a membrane.

S A Teter1, D J Klionsky.   

Abstract

Several protein-targeting fields have recently converged in their observations of what once was thought to be a rare phenomenon: the transport of folded and oligomerized proteins across membranes. Three of the newly characterized pathways that are known to accommodate folded substrates are the peroxisomal targeting machinery for matrix proteins, the twin-arginine translocation (Tat) of bacteria and the related DeltapH-dependent pathway of plant plastids, and the cytoplasm-to-vacuole targeting (Cvt) pathway in Saccharomyces cerevisiae. Current work strives to understand the molecular mechanisms that accomplish transport of folded substrates. The aim of this commentary is to highlight our knowledge of transport mechanisms, point out areas for future research and address how paradigms of classical protein translocation have shaped current views.

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Year:  1999        PMID: 10511706     DOI: 10.1016/s0962-8924(99)01652-9

Source DB:  PubMed          Journal:  Trends Cell Biol        ISSN: 0962-8924            Impact factor:   20.808


  13 in total

1.  Folded HasA inhibits its own secretion through its ABC exporter.

Authors:  L Debarbieux; C Wandersman
Journal:  EMBO J       Date:  2001-09-03       Impact factor: 11.598

Review 2.  Cancer chemotherapy--ribonucleases to the rescue.

Authors:  P A Leland; R T Raines
Journal:  Chem Biol       Date:  2001-05

3.  Thylakoid targeting of Tat passenger proteins shows no delta pH dependence in vivo.

Authors:  Giovanni Finazzi; Claudia Chasen; Francis-André Wollman; Catherine de Vitry
Journal:  EMBO J       Date:  2003-02-17       Impact factor: 11.598

4.  Translocation of alpha-synuclein expressed in Escherichia coli.

Authors:  Guoping Ren; Xi Wang; Shufeng Hao; Hongyu Hu; Chih-Chen Wang
Journal:  J Bacteriol       Date:  2007-02-02       Impact factor: 3.490

5.  Translocation of mitochondrially synthesized Cox2 domains from the matrix to the intermembrane space.

Authors:  Heather L Fiumera; Sarah A Broadley; Thomas D Fox
Journal:  Mol Cell Biol       Date:  2007-04-23       Impact factor: 4.272

6.  The canonical twin-arginine translocase components are not required for secretion of folded green fluorescent protein from the ancestral strain of Bacillus subtilis.

Authors:  Anthony J Snyder; Sampriti Mukherjee; J Kyle Glass; Daniel B Kearns; Suchetana Mukhopadhyay
Journal:  Appl Environ Microbiol       Date:  2014-03-14       Impact factor: 4.792

7.  Vacuolar localization of oligomeric alpha-mannosidase requires the cytoplasm to vacuole targeting and autophagy pathway components in Saccharomyces cerevisiae.

Authors:  M U Hutchins; D J Klionsky
Journal:  J Biol Chem       Date:  2001-03-22       Impact factor: 5.157

8.  Peripheral mitochondrial inner membrane protein, Mss2p, required for export of the mitochondrially coded Cox2p C tail in Saccharomyces cerevisiae.

Authors:  S A Broadley; C M Demlow; T D Fox
Journal:  Mol Cell Biol       Date:  2001-11       Impact factor: 4.272

9.  Cell adhesion molecule DdCAD-1 is imported into contractile vacuoles by membrane invagination in a Ca2+- and conformation-dependent manner.

Authors:  Shrivani Sriskanthadevan; Teresa Lee; Zhi Lin; Daiwen Yang; Chi-Hung Siu
Journal:  J Biol Chem       Date:  2009-10-29       Impact factor: 5.157

10.  The twin-arginine signal peptide of Bacillus subtilis YwbN can direct either Tat- or Sec-dependent secretion of different cargo proteins: secretion of active subtilisin via the B. subtilis Tat pathway.

Authors:  Marc A B Kolkman; René van der Ploeg; Michael Bertels; Maurits van Dijk; Joop van der Laan; Jan Maarten van Dijl; Eugenio Ferrari
Journal:  Appl Environ Microbiol       Date:  2008-10-17       Impact factor: 4.792

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