Abstract
Ionophoric activities of an N-terminus truncated gramicidin A (gA) analogue (mini-gramicidin) and its covalent dimer were studied in planar bilayer phospholipid membranes (BLM) using macroscopic current measurements (at high concentrations of the peptides) and single-channel recordings. As with gA-induced currents, mini-gramicidin-stimulated macroscopic currents through BLM underwent sensitized photoinactivation, i.e. were suppressed after irradiation with visible light in the presence of a photosensitizer generating singlet oxygen. The sensitivity of the tested compounds to photoinactivation descended in the following order: minigramicidin dimer > mini-gramicidin monomer > gA. The data from single-channel measurements and kinetic analysis of flash-induced photoinactivation obtained at different levels of macroscopic currents suggest that mini-gramicidin and its covalent dimer induce a variety of conducting states; their ratio depends on membrane thickness. Analysis of natural (mitochondrial and erythrocyte) membranes established that ionophoric activities of mini-gramicidin and its covalent dimer depend essentially on the membrane type.
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Abbreviations
- BLM:
-
bilayer lipid membrane
- AlPcS3 :
-
trisulfonated aluminum phthalocyanine
- DPhPC:
-
diphytanoylphosphaditylcholine
- POPC:
-
palmitoyloleoylphosphaditylcholine
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Original Russian Text © E.A. Dutseva, E.A. Kotova, Yu.N. Antonenko, 2008, published in Biologicheskie Membrany, 2008, Vol. 25, No. 1, pp. 58–65.
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Dutseva, E.A., Kotova, E.A. & Antonenko, Y.N. Ionophoric activity of truncated gramicidin A analogue in phospholipid bilayers and mitochondrial and erythrocyte membranes. Biochem. Moscow Suppl. Ser. A 2, 55–61 (2008). https://doi.org/10.1007/s11827-008-1009-4
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DOI: https://doi.org/10.1007/s11827-008-1009-4