Literature DB >> 6094818

Single-length and double-length channels formed by nystatin in lipid bilayer membranes.

M E Kleinberg, A Finkelstein.   

Abstract

Nystatin forms two types of channels in sterol-containing planar bilayer membranes. One type is formed when it is added to only one side of the membrane; the other is formed when it is added to both sides of the membrane. The relative permeability of these channels to nonelectrolytes (urea and glycerol) is identical. The sensitivity of membranes to the one-sided action of nystatin is critically dependent on their thickness; in particular, membranes made from monoglycerides with more than 18 carbon atoms in their acyl chain are insensitive to nystatin's one-sided action. These data are consistent with a model in which the two types of channels formed by nystatin have essentially identical structures, except that the channel formed by its two-sided action is twice the length of that formed by its one-sided action, because it is a tail-to-tail dimer of the latter.

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Year:  1984        PMID: 6094818     DOI: 10.1007/bf01868444

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  18 in total

1.  The thickness, composition and structure of some lipid bilayers and natural membranes.

Authors:  R Fettiplace; D M Andrews; D A Haydon
Journal:  J Membr Biol       Date:  1971-09       Impact factor: 1.843

2.  Electrical capacity of black lipid films and of lipid bilayers made from monolayers.

Authors:  R Benz; O Fröhlich; P Läuger; M Montal
Journal:  Biochim Biophys Acta       Date:  1975-07-03

3.  Fusion of phospholipid vesicles reconstituted with cytochrome c oxidase and mitochondrial hydrophobic protein.

Authors:  C Miller; E Racker
Journal:  J Membr Biol       Date:  1976-05       Impact factor: 1.843

4.  Separation of polyene antifungal antibiotics by high-speed liquid chromatography.

Authors:  W Mechlinski; C P Schaffner
Journal:  J Chromatogr       Date:  1974-11-06

5.  Equilibrium dialysis of ions in nystatin-treated red cells.

Authors:  A Cass; M Dalmark
Journal:  Nat New Biol       Date:  1973-07-11

6.  Sequence of candicidin action on yeast cells.

Authors:  P Liras; J O Lampen
Journal:  Biochim Biophys Acta       Date:  1974-11-04

7.  Effect of amphotericin B on cholesterol-containing liposomes of egg phosphatidylcholine and didocosenoyl phosphatidylcholine. A refinement of the model for the formation of pores by amphotericin B in membranes.

Authors:  P van Hoogevest; B de Kruijff
Journal:  Biochim Biophys Acta       Date:  1978-08-17

8.  Characterization of aromatic heptaene macrolide antibiotics by high performance liquid chromatography.

Authors:  W Mechlinski; C P Schaffner
Journal:  J Antibiot (Tokyo)       Date:  1980-06       Impact factor: 2.649

9.  The interaction of polyene antibiotics with thin lipid membranes.

Authors:  T E Andreoli; M Monahan
Journal:  J Gen Physiol       Date:  1968-08       Impact factor: 4.086

10.  The water and nonelectrolyte permeability induced in thin lipid membranes by the polyene antibiotics nystatin and amphotericin B.

Authors:  R Holz; A Finkelstein
Journal:  J Gen Physiol       Date:  1970-07       Impact factor: 4.086

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  38 in total

1.  Inward rectifier K(+) current under physiological cytoplasmic conditions in guinea-pig cardiac ventricular cells.

Authors:  Keiko Ishihara; Ding-Hong Yan; Shintaro Yamamoto; Tsuguhisa Ehara
Journal:  J Physiol       Date:  2002-05-01       Impact factor: 5.182

2.  Contribution of cyclic-nucleotide-gated channels to the resting conductance of olfactory receptor neurons.

Authors:  Raymund Y K Pun; Steven J Kleene
Journal:  Biophys J       Date:  2003-05       Impact factor: 4.033

3.  Comparative drug disposition, urinary pharmacokinetics, and renal effects of multilamellar liposomal nystatin and amphotericin B deoxycholate in rabbits.

Authors:  Andreas H Groll; Diana Mickiene; Vidmantas Petraitis; Ruta Petraitiene; Raul M Alfaro; Christine King; Stephen C Piscitelli; Thomas J Walsh
Journal:  Antimicrob Agents Chemother       Date:  2003-12       Impact factor: 5.191

4.  Small and maxi K+ channels in the basolateral membrane of isolated crypts from rat distal colon: single-channel and slow whole-cell recordings.

Authors:  B C Burckhardt; H Gögelein
Journal:  Pflugers Arch       Date:  1992-01       Impact factor: 3.657

5.  Effect of membrane structure on the action of polyenes: I. Nystatin action in cholesterol- and ergosterol-containing membranes.

Authors:  K S Récamier; A Hernández-Gómez; J González-Damián; I Ortega-Blake
Journal:  J Membr Biol       Date:  2010-09-26       Impact factor: 1.843

6.  Diffusion of nystatin in plasma membrane is inhibited by a glass-membrane seal.

Authors:  R Horn
Journal:  Biophys J       Date:  1991-08       Impact factor: 4.033

7.  Pore formation by Staphylococcus aureus alpha-toxin in lipid bilayers. Dependence upon temperature and toxin concentration.

Authors:  G Belmonte; L Cescatti; B Ferrari; T Nicolussi; M Ropele; G Menestrina
Journal:  Eur Biophys J       Date:  1987       Impact factor: 1.733

8.  Voltage-dependent channel formation by rods of helical polypeptides.

Authors:  G Menestrina; K P Voges; G Jung; G Boheim
Journal:  J Membr Biol       Date:  1986       Impact factor: 1.843

9.  Inactivation by ionizing radiation of ion channels formed by polyene antibiotics amphotericin B and nystatin in lipid membranes: an inverse dose-rate behavior.

Authors:  C Barth; G Stark; M Wilhelm
Journal:  Biophys J       Date:  1993-01       Impact factor: 4.033

10.  Dual action of leptin on rest-firing and stimulated catecholamine release via phosphoinositide 3-kinase-driven BK channel up-regulation in mouse chromaffin cells.

Authors:  Daniela Gavello; David Vandael; Sara Gosso; Emilio Carbone; Valentina Carabelli
Journal:  J Physiol       Date:  2015-09-27       Impact factor: 5.182

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