Literature DB >> 8399284

The outer mitochondrial membrane channel, VDAC, is modulated by a protein localized in the intermembrane space.

M J Holden1, M Colombini.   

Abstract

The mitochondrial outer membrane channel, VDAC, provides a pathway for the flux of metabolites between the cytoplasm and mitochondrion. VDAC is voltage-dependent and occupies states of differing conductivity and ion selectivity that are dependent on transmembrane potential. A protein, derived from preparations of mitochondria, has been shown to increase the voltage dependence of VDAC and is called the VDAC modulator. Both VDAC and the VDAC modulator have been extensively characterized by reconstitution into planar lipid bilayers. In order for the VDAC modulator to have physiological significance it must have physical access to VDAC in the cell. This constraint dictates that the modulator be an extrinsic outer mitochondrial membrane protein, occupy the mitochondrial intermembrane space, or be a cytoplasmic constituent. To address the question of subcellular localization, purified mitochondria were selectively lysed with digitonin or treated with trypsin while resuspended in hypo-osmotic or iso-osmotic medium. Marker enzymes and modulator activity were monitored during the various treatments. Results indicate that the integrity of the outer membrane was necessary to prevent modulator release or protection from trypsin digestion. Outer membrane lysis, under conditions where the inner membrane remained intact, resulted in modulator release or inactivation by trypsin. These results suggest an intermembrane space location for the VDAC modulator in the mitochondrion.

Entities:  

Mesh:

Substances:

Year:  1993        PMID: 8399284     DOI: 10.1016/0005-2728(93)90126-z

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  19 in total

1.  Metabolically derived potential on the outer membrane of mitochondria: a computational model.

Authors:  S V Lemeshko; V V Lemeshko
Journal:  Biophys J       Date:  2000-12       Impact factor: 4.033

2.  The role of sterols in the functional reconstitution of water-soluble mitochondrial porins from plants.

Authors:  F Carbonara; B Popp; A Schmid; V Iacobazzi; G Genchi; F Palmieri; R Benz
Journal:  J Bioenerg Biomembr       Date:  1996-04       Impact factor: 2.945

3.  Intracellular localization of VDAC proteins in plants.

Authors:  Cathrin Clausen; Iryna Ilkavets; Rowena Thomson; Katrin Philippar; Aleksandar Vojta; Torsten Möhlmann; Ekkehard Neuhaus; Hrvoje Fulgosi; Jürgen Soll
Journal:  Planta       Date:  2004-07-16       Impact factor: 4.116

4.  Functional characterization of the conserved "GLK" motif in mitochondrial porin from Neurospora crassa.

Authors:  G Runke; E Maier; J D O'Neil; R Benz; D A Court
Journal:  J Bioenerg Biomembr       Date:  2000-12       Impact factor: 2.945

5.  Theoretical evaluation of a possible nature of the outer membrane potential of mitochondria.

Authors:  Victor V Lemeshko
Journal:  Eur Biophys J       Date:  2006-10-05       Impact factor: 1.733

Review 6.  Mitochondrial ion channels.

Authors:  Brian O'Rourke
Journal:  Annu Rev Physiol       Date:  2007       Impact factor: 19.318

7.  Multicopy suppressors of phenotypes resulting from the absence of yeast VDAC encode a VDAC-like protein.

Authors:  E Blachly-Dyson; J Song; W J Wolfgang; M Colombini; M Forte
Journal:  Mol Cell Biol       Date:  1997-10       Impact factor: 4.272

8.  VDAC closure increases calcium ion flux.

Authors:  Wenzhi Tan; Marco Colombini
Journal:  Biochim Biophys Acta       Date:  2007-06-12

Review 9.  Reflections on VDAC as a voltage-gated channel and a mitochondrial regulator.

Authors:  Carmen A Mannella; Kathleen W Kinnally
Journal:  J Bioenerg Biomembr       Date:  2008-06       Impact factor: 2.945

10.  Modulation of the voltage-dependent anion channel (VDAC) by glutamate.

Authors:  D Gincel; S D Silberberg; V Shoshan-Barmatz
Journal:  J Bioenerg Biomembr       Date:  2000-12       Impact factor: 2.945

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.