Bilayer-dependent inhibition of mechanosensitive channels by neuroactive peptide enantiomers

by Suchyna, T. M.; Tape, S. E.; Koeppe, R. E.; Andersen, O. S.; Sachs, F.; Gottlieb, P. A.

The peptide GsMTx4, isolated from the venom of the tarantula Grammostola spatulata, is a selective inhibitor of stretch-activated cation channels (SACs)(1). The mechanism of inhibition remains unknown; but both GsMTx4 and its enantiomer, enGsMTx4, modify the gating of SACs, thus violating a trademark of the traditional lock-and-key model of ligand-protein interactions. Suspecting a bilayer-dependent mechanism, we examined the effect of GsMTx4 and enGsMTx4 on gramicidin A (gA) channel gating(2). Both peptides are active, and the effect increases with the degree of hydrophobic mismatch between bilayer thickness and channel length, meaning that GsMTx4 decreases the energy required to deform the boundary lipids adjacent to the channel. GsMTx4 decreases inward SAC single-channel currents but has no effect on outward currents, suggesting it is located within a Debye length of the outer vestibule of the SACs, but significantly farther from the inner vestibule. Likewise, GsMTx4 decreases gA single-channel currents. Our results suggest that modulation of membrane proteins by amphipathic peptides-mechanopharmacology-involves not only the protein itself but also the surrounding lipids. The surprising efficacy of the D form of GsMTx4 peptide has important therapeutic implications, because D peptides are not hydrolysed by endogenous proteases and may be administered orally.

Journal
Nature
Volume
430
Issue
6996
Year
2004
Start Page
235-240
URL
https://dx.doi.org/10.1038/nature02743
ISBN/ISSN
1476-4687; 0028-0836
DOI
10.1038/nature02743