Modulation of the mitochondrial voltage dependent anion channel (VDAC) by curcumin
pmid: 25459681
Modulation of the mitochondrial voltage dependent anion channel (VDAC) by curcumin
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.
Curcumin, Vdac, Blotting, Western, Lipid Bilayers, Biophysics, Apoptosis, Biochemistry, Protein Structure, Secondary, Bcl-2 Family, Mitochondrial Proteins, Ion Channel, Mechanisms, Animals, Humans, Cell-Death, Permeability Transition, Binding Sites, VDAC, Dose-Response Relationship, Drug, Molecular Structure, Circular Dichroism, Voltage-Dependent Anion Channel 1, Membrane, Proteins, Cell Biology, Mitochondria, Protein Structure, Tertiary, Molecular Docking Simulation, Bax, Spectrophotometry, Mutation, Cattle, Involvement, Ion channel, Gating, Ion Channel Gating, Cytochrome-C Release, Protein Binding
Curcumin, Vdac, Blotting, Western, Lipid Bilayers, Biophysics, Apoptosis, Biochemistry, Protein Structure, Secondary, Bcl-2 Family, Mitochondrial Proteins, Ion Channel, Mechanisms, Animals, Humans, Cell-Death, Permeability Transition, Binding Sites, VDAC, Dose-Response Relationship, Drug, Molecular Structure, Circular Dichroism, Voltage-Dependent Anion Channel 1, Membrane, Proteins, Cell Biology, Mitochondria, Protein Structure, Tertiary, Molecular Docking Simulation, Bax, Spectrophotometry, Mutation, Cattle, Involvement, Ion channel, Gating, Ion Channel Gating, Cytochrome-C Release, Protein Binding
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