Literature DB >> 10603473

Protein translocation into mitochondria: the role of TIM complexes.

M F Bauer1, S Hofmann, W Neupert, M Brunner.   

Abstract

Import of nuclear-encoded mitochondrial preproteins is mediated by a general translocase in the outer membrane, the TOM complex, and by two distinct translocases in the mitochondrial inner membrane, the TIM23 complex and the TIM22 complex. Both TIM complexes cooperate with the TOM complex but facilitate import of different classes of precursor proteins. Precursors with an N-terminal presequence are imported via the TIM23 complex, whereas mitochondrial carrier proteins require the TIM22 complex for insertion into the inner membrane. This review discusses recent advances in understanding the structure and function of the translocases of the inner membrane and the possible role of Tim proteins in the development of the Mohr-Tranebjaerg syndrome, a mitochondrial disorder leading to neurodegeneration.

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Year:  2000        PMID: 10603473     DOI: 10.1016/s0962-8924(99)01684-0

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


  60 in total

Review 1.  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

2.  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

3.  Mechanical fractionation reveals structural requirements for enteropathogenic Escherichia coli Tir insertion into host membranes.

Authors:  A Gauthier; M de Grado; B B Finlay
Journal:  Infect Immun       Date:  2000-07       Impact factor: 3.441

4.  The mitochondrial Hsp70-dependent import system actively unfolds preproteins and shortens the lag phase of translocation.

Authors:  J H Lim; F Martin; B Guiard; N Pfanner; W Voos
Journal:  EMBO J       Date:  2001-03-01       Impact factor: 11.598

5.  Membrane potential-driven protein import into mitochondria. The sorting sequence of cytochrome b(2) modulates the deltapsi-dependence of translocation of the matrix-targeting sequence.

Authors:  A Geissler; T Krimmer; U Bömer; B Guiard; J Rassow; N Pfanner
Journal:  Mol Biol Cell       Date:  2000-11       Impact factor: 4.138

6.  Mitochondrial protein import motor: the ATPase domain of matrix Hsp70 is crucial for binding to Tim44, while the peptide binding domain and the carboxy-terminal segment play a stimulatory role.

Authors:  T Krimmer; J Rassow; W H Kunau; W Voos; N Pfanner
Journal:  Mol Cell Biol       Date:  2000-08       Impact factor: 4.272

7.  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

8.  The Tim9p-Tim10p complex binds to the transmembrane domains of the ADP/ATP carrier.

Authors:  Sean P Curran; Danielle Leuenberger; Wolfgang Oppliger; Carla M Koehler
Journal:  EMBO J       Date:  2002-03-01       Impact factor: 11.598

9.  Apocytochrome c requires the TOM complex for translocation across the mitochondrial outer membrane.

Authors:  K Diekert; A I de Kroon; U Ahting; B Niggemeyer; W Neupert; B de Kruijff; R Lill
Journal:  EMBO J       Date:  2001-10-15       Impact factor: 11.598

10.  Structural requirements of Tom40 for assembly into preexisting TOM complexes of mitochondria.

Authors:  D Rapaport; R D Taylor; M Käser; T Langer; W Neupert; F E Nargang
Journal:  Mol Biol Cell       Date:  2001-05       Impact factor: 4.138

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