Bilayer-dependent inhibition of mechanosensitive channels by neuroactive peptide enantiomers

Thomas M. Suchyna, Sonya E. Tape, Roger E. Koeppe, Olaf S. Andersen (), Frederick Sachs and Philip A. Gottlieb
Additional contact information
Thomas M. Suchyna: SUNY at Buffalo
Sonya E. Tape: Weill Medical College of Cornell University
Roger E. Koeppe: University of Arkansas
Olaf S. Andersen: Weill Medical College of Cornell University
Frederick Sachs: SUNY at Buffalo
Philip A. Gottlieb: SUNY at Buffalo

Nature, 2004, vol. 430, issue 6996, 235-240

Abstract: Abstract 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 gating2. 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.

Date: 2004
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DOI: 10.1038/nature02743

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