TY - JOUR
T1 - Investigation of the electrophysiological properties of enniatins
AU - Kamyar, Majid-Reza
AU - Rawnduzi, Pakiza
AU - Studenik, Christian
AU - Kouri, Katerina
AU - Lemmens, Rosa
N1 - DOI: 10.1016/j.abb.2004.06.013
Coden: ABBIA
Affiliations: Dept. of Pharmacology and Toxicology, University of Vienna, Althanstr. 14, A-1090, Vienna, Austria
Adressen: Lemmens-Gruber, R.; Dept. of Pharmacology and Toxicology; University of Vienna; Althanstr. 14, A-1090 Vienna, Austria; email: [email protected]
Source-File: DirschHeringViernsteinScopus_iso.csv
Import aus Scopus: 2-s2.0-4143136362
Importdatum: 29.11.2006 12:33:41
09.08.2007: Datenanforderung 1812 (Import Sachbearbeiter)
PY - 2004
Y1 - 2004
N2 - Enniatins are cyclohexadepsipeptides produced by various species of the genus Fusarium, and are known to have ionophoric, antibiotic, and in vitro hypolipidaemic properties. With the patch clamp technique in the inside-out mode it could be shown that enniatin easily incorporates into the cell membrane in which it forms cation-selective pores. This feature is characterized by unitary transitions to conductance levels typical for channels, ion selectivity, rectification, conductivity in the pS range, and block. A model of vertically stacked enniatin molecules that form sandwich complexes is suggested. Like gramicidin enniatin is a passive channel. Single channel properties for the isomers enniatin A1, B, and B1 differed from each other. This implies an influence of the substituted moieties on the complexation of cations. Electrical activity was followed by changes in intracellular ion concentrations, which are consistent with depolarization of the membrane resting potential, shortening of action potential duration, and reduced contractility. Œ 2004 Elsevier Inc. All rights reserved.
AB - Enniatins are cyclohexadepsipeptides produced by various species of the genus Fusarium, and are known to have ionophoric, antibiotic, and in vitro hypolipidaemic properties. With the patch clamp technique in the inside-out mode it could be shown that enniatin easily incorporates into the cell membrane in which it forms cation-selective pores. This feature is characterized by unitary transitions to conductance levels typical for channels, ion selectivity, rectification, conductivity in the pS range, and block. A model of vertically stacked enniatin molecules that form sandwich complexes is suggested. Like gramicidin enniatin is a passive channel. Single channel properties for the isomers enniatin A1, B, and B1 differed from each other. This implies an influence of the substituted moieties on the complexation of cations. Electrical activity was followed by changes in intracellular ion concentrations, which are consistent with depolarization of the membrane resting potential, shortening of action potential duration, and reduced contractility. Œ 2004 Elsevier Inc. All rights reserved.
U2 - 10.1016/j.abb.2004.06.013
DO - 10.1016/j.abb.2004.06.013
M3 - Article
VL - 429
SP - 215
EP - 223
JO - Archives of Biochemistry and Biophysics
JF - Archives of Biochemistry and Biophysics
SN - 0003-9861
IS - 2
ER -