Literature DB >> 9774109

Tom40 forms the hydrophilic channel of the mitochondrial import pore for preproteins [see comment].

K Hill1, K Model, M T Ryan, K Dietmeier, F Martin, R Wagner, N Pfanner.   

Abstract

The mitochondrial outer membrane contains machinery for the import of preproteins encoded by nuclear genes. Eight different Tom (translocase of outer membrane) proteins have been identified that function as receptors and/or are related to a hypothetical general import pore. Many mitochondrial membrane channel activities have been described, including one related to Tim23 of the inner-membrane protein-import system; however, the pore-forming subunit(s) of the Tom machinery have not been identified until now. Here we describe the expression and functional reconstitution of Tom40, an integral membrane protein with mainly beta-sheet structure. Tom40 forms a cation-selective high-conductance channel that specifically binds to and transports mitochondrial-targeting sequences added to the cis side of the membrane. We conclude that Tom40 is the pore-forming subunit of the mitochondrial general import pore and that it constitutes a hydrophilic, approximately 22 A wide channel for the import of preproteins.

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Year:  1998        PMID: 9774109     DOI: 10.1038/26780

Source DB:  PubMed          Journal:  Nature        ISSN: 0028-0836            Impact factor:   49.962


  157 in total

1.  Transport of the ADP/ATP carrier of mitochondria from the TOM complex to the TIM22.54 complex.

Authors:  M Endres; W Neupert; M Brunner
Journal:  EMBO J       Date:  1999-06-15       Impact factor: 11.598

2.  An internal targeting signal directing proteins into the mitochondrial intermembrane space.

Authors:  K Diekert; G Kispal; B Guiard; R Lill
Journal:  Proc Natl Acad Sci U S A       Date:  1999-10-12       Impact factor: 11.205

3.  Nascent polypeptide-associated complex stimulates protein import into yeast mitochondria.

Authors:  U Fünfschilling; S Rospert
Journal:  Mol Biol Cell       Date:  1999-10       Impact factor: 4.138

Review 4.  Protein unfolding by mitochondria. The Hsp70 import motor.

Authors:  A Matouschek; N Pfanner; W Voos
Journal:  EMBO Rep       Date:  2000-11       Impact factor: 8.807

5.  Protein import channel of the outer mitochondrial membrane: a highly stable Tom40-Tom22 core structure differentially interacts with preproteins, small tom proteins, and import receptors.

Authors:  C Meisinger; M T Ryan; K Hill; K Model; J H Lim; A Sickmann; H Müller; H E Meyer; R Wagner; N Pfanner
Journal:  Mol Cell Biol       Date:  2001-04       Impact factor: 4.272

6.  Biogenesis of Tim proteins of the mitochondrial carrier import pathway: differential targeting mechanisms and crossing over with the main import pathway.

Authors:  M Kurz; H Martin; J Rassow; N Pfanner; M T Ryan
Journal:  Mol Biol Cell       Date:  1999-07       Impact factor: 4.138

7.  Tim18p is a new component of the Tim54p-Tim22p translocon in the mitochondrial inner membrane.

Authors:  O Kerscher; N B Sepuri; R E Jensen
Journal:  Mol Biol Cell       Date:  2000-01       Impact factor: 4.138

8.  The three modules of ADP/ATP carrier cooperate in receptor recruitment and translocation into mitochondria.

Authors:  N Wiedemann; N Pfanner; M T Ryan
Journal:  EMBO J       Date:  2001-03-01       Impact factor: 11.598

9.  Uncoupling of transfer of the presequence and unfolding of the mature domain in precursor translocation across the mitochondrial outer membrane.

Authors:  T Kanamori; S Nishikawa; M Nakai; I Shin; P G Schultz; T Endo
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

10.  L and D presequence peptides derived from the precursor of F1beta subunit of the ATP synthase inhibit mitochondrial protein import by interaction with import machinery.

Authors:  C Sigyarto; M Hugosson; P Moberg; D Andreu; E Glaser
Journal:  Plant Mol Biol       Date:  2001-12       Impact factor: 4.076

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