Literature DB >> 1833391

Role of an energized inner membrane in mitochondrial protein import. Delta psi drives the movement of presequences.

J Martin1, K Mahlke, N Pfanner.   

Abstract

The transport of precursor proteins into mitochondria requires an energized inner membrane. We report here that the import of various precursor proteins showed a differential sensitivity to treatment of the mitochondria with the uncoupler carbonyl cyanide m-chlorophenylhydrazone. The differential inhibition by carbonyl cyanide m-chlorophenylhydrazone was not influenced by the length of the precursor, the presence of mature protein parts, or the folding state of the precursor but was specific for the presequence. Moreover, only the membrane potential delta psi and not the total proton motive force was required for the transport of precursors, indicating that protein translocation across the inner membrane is not driven by a movement of protons. We conclude that delta psi (negative inside) is needed for the translocation of the positively charged presequences, possibly via an electrophoretic effect.

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Year:  1991        PMID: 1833391

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  117 in total

1.  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

2.  Protein import into plant mitochondria: precursor proteins differ in ATP and membrane potential requirements.

Authors:  M Tanudji; P Dessi; M Murcha; J Whelan
Journal:  Plant Mol Biol       Date:  2001-02       Impact factor: 4.076

Review 3.  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

4.  Chemical cleavage of the overexpressed mitochondrial F1beta precursor with CNBr: a new strategy to construct an import-competent preprotein.

Authors:  P F Pavlov; P Moberg; X P Zhang; E Glaser
Journal:  Biochem J       Date:  1999-07-01       Impact factor: 3.857

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

Review 8.  MCC and PSC, the putative protein import channels of mitochondria.

Authors:  K W Kinnally; C Muro; M L Campo
Journal:  J Bioenerg Biomembr       Date:  2000-02       Impact factor: 2.945

9.  TAT fusion protein transduction into isolated mitochondria is accelerated by sodium channel inhibitors.

Authors:  Jayanagendra P Rayapureddi; Wendy J Tomamichel; Sonia T Walton; R Mark Payne
Journal:  Biochemistry       Date:  2010-11-09       Impact factor: 3.162

10.  Mitochondria use different mechanisms for transport of multispanning membrane proteins through the intermembrane space.

Authors:  Ann E Frazier; Agnieszka Chacinska; Kaye N Truscott; Bernard Guiard; Nikolaus Pfanner; Peter Rehling
Journal:  Mol Cell Biol       Date:  2003-11       Impact factor: 4.272

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