Abstract
Voltage dependent anion channel (VDAC) of mitochondria plays a crucial role in apoptosis. Human VDAC-1, reconstituted in planar lipid bilayer showed reduced conductance when treated with curcumin. Curcumin interacts with residues in the α helical N-terminus of VDAC and in the channel wall, as revealed by molecular docking, followed by mutational analysis. N-terminus mimicking peptide showed conformational changes in circular dichroism, upon curcumin treatment. We propose that the interaction of curcumin with amino acids in N-terminus and in channel wall fixes the α helix in closed conformation. This restricts its movement which is required for the opening of the channel.
Keywords:
Apoptosis; Curcumin; Gating; Ion channel; Mitochondria; VDAC.
Copyright © 2014 Elsevier B.V. All rights reserved.
Publication types
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Research Support, Non-U.S. Gov't
MeSH terms
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Animals
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Binding Sites / genetics
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Blotting, Western
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Cattle
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Circular Dichroism
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Curcumin / chemistry
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Curcumin / metabolism
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Curcumin / pharmacology*
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Dose-Response Relationship, Drug
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Humans
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Ion Channel Gating / drug effects
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Ion Channel Gating / genetics
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Ion Channel Gating / physiology
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Lipid Bilayers / chemistry
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Lipid Bilayers / metabolism
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Mitochondria / drug effects*
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Mitochondria / metabolism
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Mitochondrial Proteins / chemistry*
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Mitochondrial Proteins / genetics
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Mitochondrial Proteins / metabolism
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Molecular Docking Simulation
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Molecular Structure
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Mutation
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Protein Binding
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Protein Structure, Secondary
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Protein Structure, Tertiary
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Spectrophotometry
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Voltage-Dependent Anion Channel 1 / chemistry*
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Voltage-Dependent Anion Channel 1 / genetics
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Voltage-Dependent Anion Channel 1 / metabolism
Substances
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Lipid Bilayers
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Mitochondrial Proteins
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VDAC1 protein, human
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Voltage-Dependent Anion Channel 1
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Curcumin