Literature DB >> 2444711

Elimination and restoration of voltage dependence in the mitochondrial channel, VDAC, by graded modification with succinic anhydride.

D M Adelsberger-Mangan1, M Colombini.   

Abstract

The major permeability pathways of the outer mitochondrial membrane are the voltage-gated channels called VDAC. It is known that the conductance of these channels decreases as the transmembrane voltage is increased in the positive or negative direction. These channels are known to display a preference for anions over cations of similar size and valence. It was proposed (Doring & Colombini, 1985b) that a set of positive charges lining the channel may be responsible for both voltage dependence and selectivity. A prediction of this proposal is that progressive replacement of the positive charges with negative charges should at first diminish, and then restore, voltage dependence. At the same time, the channel's preference for anions over cations should diminish then reverse. Succinic anhydride was used to perform these experiments as it replaces positively charged amino groups with negatively charged carboxyl groups. When channels, which had been inserted into phospholipid membranes, were treated with moderate amounts of the anhydride, they lost their voltage dependence and preference for anions. With further succinylation, voltage dependence was regenerated while the channels became cation selective. The voltage needed to close one-half of the channels increased in those treatments in which voltage dependence was diminished. As voltage dependence was restored, the voltage needed to close half of the channels decreased. The energy difference between the open and closed state in the absence of an applied field changed little with succinylation, indicating that the procedure did not cause large changes in VDAC's structure but specifically altered those charges responsible for voltage gating and selectivity.

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Year:  1987        PMID: 2444711     DOI: 10.1007/bf01872128

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


  25 in total

1.  The mitochondrial voltage-dependent channel, VDAC, is modified asymmetrically by succinic anhydride.

Authors:  C Doring; M Colombini
Journal:  J Membr Biol       Date:  1985       Impact factor: 1.843

2.  Characteristics of isolated and purified preparations of the outer and inner membranes of mitochondria.

Authors:  D F Parsons; G R Williams; B Chance
Journal:  Ann N Y Acad Sci       Date:  1966-07-14       Impact factor: 5.691

3.  Voltage-dependent channels found in the membrane fraction of corn mitochondria.

Authors:  D P Smack; M Colombini
Journal:  Plant Physiol       Date:  1985-12       Impact factor: 8.340

4.  Batrachotoxin modifies the gating kinetics of sodium channels in internally perfused neuroblastoma cells.

Authors:  L Y Huang; N Moran; G Ehrenstein
Journal:  Proc Natl Acad Sci U S A       Date:  1982-03       Impact factor: 11.205

5.  Hydrodynamic properties of porin isolated from outer membranes of rat liver mitochondria.

Authors:  M Lindén; P Gellerfors
Journal:  Biochim Biophys Acta       Date:  1983-12-07

6.  Structure and mode of action of a voltage dependent anion-selective channel (VDAC) located in the outer mitochondrial membrane.

Authors:  M Colombini
Journal:  Ann N Y Acad Sci       Date:  1980       Impact factor: 5.691

7.  Reconstitution in planar lipid bilayers of a voltage-dependent anion-selective channel obtained from paramecium mitochondria.

Authors:  S J Schein; M Colombini; A Finkelstein
Journal:  J Membr Biol       Date:  1976-12-28       Impact factor: 1.843

8.  Purification and characterisation of a pore protein of the outer mitochondrial membrane from Neurospora crassa.

Authors:  H Freitag; W Neupert; R Benz
Journal:  Eur J Biochem       Date:  1982-04

9.  The nature of the negative resistance in bimolecular lipid membranes containing excitability-inducing material.

Authors:  G Ehrenstein; H Lecar; R Nossal
Journal:  J Gen Physiol       Date:  1970-01       Impact factor: 4.086

10.  Structure of the outer mitochondrial membrane: ordered arrays of porelike subunits in outer-membrane fractions from Neurospora crassa mitochondria.

Authors:  C A Mannella
Journal:  J Cell Biol       Date:  1982-09       Impact factor: 10.539

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  6 in total

1.  A soluble mitochondrial protein increases the voltage dependence of the mitochondrial channel, VDAC.

Authors:  M Y Liu; M Colombini
Journal:  J Bioenerg Biomembr       Date:  1992-02       Impact factor: 2.945

2.  Zero-current potentials in a large membrane channel: a simple theory accounts for complex behavior.

Authors:  E B Zambrowicz; M Colombini
Journal:  Biophys J       Date:  1993-09       Impact factor: 4.033

3.  Voltage gating in VDAC is markedly inhibited by micromolar quantities of aluminum.

Authors:  E T Dill; M J Holden; M Colombini
Journal:  J Membr Biol       Date:  1987       Impact factor: 1.843

Review 4.  Voltage gating in the mitochondrial channel, VDAC.

Authors:  M Colombini
Journal:  J Membr Biol       Date:  1989-10       Impact factor: 1.843

5.  Activation of bovine tracheal chloride channels by amino group-specific reagents.

Authors:  M Duszyk; Y Shu; A K Ho; S F Man
Journal:  J Physiol       Date:  1998-10-01       Impact factor: 5.182

6.  Large scale rearrangement of protein domains is associated with voltage gating of the VDAC channel.

Authors:  S Peng; E Blachly-Dyson; M Forte; M Colombini
Journal:  Biophys J       Date:  1992-04       Impact factor: 4.033

  6 in total

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