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This work engineered three peptides and demonstrated that they all characteristically block VDAC reconstituted into planar lipid membranes in a controllable manner, thereby mimicking the actions of tubulin and αSyn.
Comparative analysis of α-synuclein interaction with three mammalian VDAC isoforms, complemented by corresponding data for VDAC2 substates and results from molecular dynamics simulations, reveals a new step in the chain of events leading to VDAC blockage.
The results demonstrate the metabolism-dependent generation of ΔΨMOM and provide strong evidence that VDAC regulation by voltage, observed in in vitro studies, is highly relevant to cell physiology.
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