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D. Hoogerheide

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Open access Oct 2026

Towards VDAC pharmacology: Developing small-peptide channel inhibitors inspired by nature

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.

T. Rostovtseva, P. Gurnev, D. Hoogerheide et al. · 0 citations

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