Regulation of metabolite flux through voltage-gating of VDAC channels

被引:229
|
作者
Hodge, T [1 ]
Colombini, M [1 ]
机构
[1] UNIV MARYLAND,DEPT ZOOL,CELL BIOL LABS,COLLEGE PK,MD 20742
来源
JOURNAL OF MEMBRANE BIOLOGY | 1997年 / 157卷 / 03期
关键词
mitochondria; outer membrane; ion flux; VDAC; channel; gating;
D O I
10.1007/s002329900235
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:271 / 279
页数:9
相关论文
共 50 条
  • [21] Opposite Cx32 and Cx26 Voltage-Gating Response to CO2 Reflects Opposite Voltage-Gating Polarity
    K.C. Young
    C. Peracchia
    The Journal of Membrane Biology, 2004, 202 : 161 - 170
  • [22] THE VOLTAGE GATING OF VDAC IS SENSITIVE TO ION FLOW
    ZIZI, M
    BYRD, C
    COLOMBINI, M
    BIOPHYSICAL JOURNAL, 1994, 66 (02) : A247 - A247
  • [23] Opposite Cx32 and Cx26 voltage-gating response to CO2 reflects opposite voltage-gating polarity
    Young, KC
    Peracchia, C
    JOURNAL OF MEMBRANE BIOLOGY, 2004, 202 (03): : 161 - 170
  • [24] Allosteric voltage-gating and the effects of calcium on mSlo Ca2+-activated K+ channels.
    Horrigan, FT
    Aldrich, RW
    BIOPHYSICAL JOURNAL, 1998, 74 (02) : A218 - A218
  • [25] Purinergic control of lysenin's transport and voltage-gating properties
    Bryant, Sheenah
    Shrestha, Nisha
    Carnig, Paul
    Kosydar, Samuel
    Belzeski, Philip
    Hanna, Charles
    Fologea, Daniel
    PURINERGIC SIGNALLING, 2016, 12 (03) : 549 - 559
  • [26] Mechanism of voltage-gating in alamethicin: NMR studies of structural variants
    Jacob, J
    Cafiso, DS
    BIOPHYSICAL JOURNAL, 1997, 72 (02) : TH294 - TH294
  • [27] Solving the Gating Mechanism of the Mitochondrial β-Barrel Metabolite Channel VDAC
    Queralt-Martin, Maria
    Ngo, Van A.
    Bergdoll, Lucie A.
    Abramson, Jeff
    Hoogerheide, David P.
    Rostovtseva, Tatiana K.
    Bezrukov, Sergey M.
    Noskov, Sergei Y.
    BIOPHYSICAL JOURNAL, 2020, 118 (03) : 269A - 269A
  • [28] Conformational rearrangements in the second voltage sensor domain switch PIP2-and voltage-gating modes in two-pore channels
    Shimomura, Takushi
    Hirazawa, Kiichi
    Kubo, Yoshihiro
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2023, 120 (06) : e2209569120
  • [29] A Stochastic Model of Voltage-Gating of Connexin-Based Gap Junction Channels Containing Fast and Slow Gates
    Paulauskas, Nerijus
    Pranevicius, Henrikas
    Bukauskas, Feliksas
    BIOPHYSICAL JOURNAL, 2011, 100 (03) : 564 - 564
  • [30] The voltage-gating process of the voltage-dependent anion channel is sensitive to ion flow
    Zizi, M
    Byrd, C
    Boxus, R
    Colombini, M
    BIOPHYSICAL JOURNAL, 1998, 75 (02) : 704 - 713