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.
· bioRxiv · 0 citations