Literature DB >> 9178614

Regulation of metabolite flux through voltage-gating of VDAC channels.

T Hodge1, M Colombini.   

Abstract

The mitochondrial outer membrane channel, VDAC, is thought to serve as the major permeability pathway for metabolite flux between the cytoplasm and mitochondria. The permeability of VDAC to citrate, succinate, and phosphate was studied in channels reconstituted into planar phospholipid membranes. All ions showed large changes in permeability depending on whether the channel was in the open or in the low conductance, "closed" state, with the closed state always more cation selective. This was especially true for the divalent and trivalent anions. Additionally, the anion flux when the voltage was zero was shown to decrease to 5-11% of the open state flux depending on the anion studied. These results give the first rigorous examination of the ability of metabolites to permeate through VDAC channels and indicate that these channels can control the flux of these ions through the outer membrane. This lends more evidence to the growing body of experiments that suggest that the outer mitochondrial membrane has a much more important role in controlling mitochondrial activity than has been thought historically.

Entities:  

Mesh:

Substances:

Year:  1997        PMID: 9178614     DOI: 10.1007/s002329900235

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  103 in total

1.  Outer mitochondrial membrane permeability can regulate coupled respiration and cell survival.

Authors:  M G Vander Heiden; N S Chandel; X X Li; P T Schumacker; M Colombini; C B Thompson
Journal:  Proc Natl Acad Sci U S A       Date:  2000-04-25       Impact factor: 11.205

Review 2.  Pathophysiological and protective roles of mitochondrial ion channels.

Authors:  B O'Rourke
Journal:  J Physiol       Date:  2000-11-15       Impact factor: 5.182

3.  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

4.  Model of the outer membrane potential generation by the inner membrane of mitochondria.

Authors:  Victor V Lemeshko
Journal:  Biophys J       Date:  2002-02       Impact factor: 4.033

5.  The hypoxic preconditioning agent deferoxamine induces poly(ADP-ribose) polymerase-1-dependent inhibition of the mitochondrial respiratory chain.

Authors:  Ana Cañuelo; Rubén Martínez-Romero; Esther Martínez-Lara; José A Sánchez-Alcázar; Eva Siles
Journal:  Mol Cell Biochem       Date:  2011-12-07       Impact factor: 3.396

6.  The voltage-dependent anion channel as a biological transistor: theoretical considerations.

Authors:  V V Lemeshko; S V Lemeshko
Journal:  Eur Biophys J       Date:  2003-10-23       Impact factor: 1.733

7.  Functional interaction of endothelial nitric oxide synthase with a voltage-dependent anion channel.

Authors:  Jianxin Sun; James K Liao
Journal:  Proc Natl Acad Sci U S A       Date:  2002-09-12       Impact factor: 11.205

8.  VDAC: the channel at the interface between mitochondria and the cytosol.

Authors:  Marco Colombini
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

9.  Energy flux modulation on the outer membrane of mitochondria by metabolically-derived potential.

Authors:  Sergy V Lemeshko; Victor V Lemeshko
Journal:  Mol Cell Biochem       Date:  2004 Jan-Feb       Impact factor: 3.396

10.  The expression level of the voltage-dependent anion channel controls life and death of the cell.

Authors:  Salah Abu-Hamad; Sara Sivan; Varda Shoshan-Barmatz
Journal:  Proc Natl Acad Sci U S A       Date:  2006-04-03       Impact factor: 11.205

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.