Literature DB >> 414780

Alteration by cereolysin of the structure of cholesterol-containing membranes.

J L Cowell, K S Kim, A W Bernheimer.   

Abstract

When erythrocyte membranes were treated with cereolysin, negatively stained and examined by electron microscopy, ring and arc-shaped structures were observed in the membrane. The outside diameter of the rings varied from 33 to 50 nm with a border thickness of 6.7 to 8.3 nm. The arcs varied in length from 33 to 170 nm with a border thickness of also 6.7 to 8.3 min. When right-side-out erythrocyte ghosts which had been treated with cereolysin were examined by electron microscopy after freeze-fracture, structures with a diameter of 31 to 63 nm were seen in the fracture face of the exoplasmic half of the membrane, but no alterations were visible in the fracture face of the protoplasmic half of the membrane bilayer. Thus the ring structures did not appear to form holes through the membrane. At cereolysin concentrations above 6 microgram/ml rings and arcs were seen when purified toxin alone was examined. At or below 6 microgram/ml toxin rings and arcs were seen only if toxin was incubated with free or membrane-bound cholesterol. Our interpretation is that cereolysin tends to aggregate into ring and arc-shaped structures, and that the tendency to aggregate is increased by cholesterol. Rings and arcs were not seen when erythrocyte ghosts were treated with low, but lytic amounts of cereolysin that significantly altered the premeability of the ghosts.

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Year:  1978        PMID: 414780     DOI: 10.1016/0005-2736(78)90419-4

Source DB:  PubMed          Journal:  Biochim Biophys Acta        ISSN: 0006-3002


  12 in total

1.  Transmembrane diffusion channels in Mycoplasma gallisepticum induced by tetanolysin.

Authors:  S Rottem; K Groover; W H Habig; M F Barile; M C Hardegree
Journal:  Infect Immun       Date:  1990-03       Impact factor: 3.441

2.  Formation of ring-shaped structures on erythrocyte membranes after treatment with botulinolysin, a thiol-activated hemolysin from Clostridium botulinum.

Authors:  K Sekiya; H Danbara; Y Futaesaku; A Haque; N Sugimoto; M Matsuda
Journal:  Infect Immun       Date:  1998-06       Impact factor: 3.441

3.  Electron microscopic evaluation of a two-step theory of pore formation by streptolysin O.

Authors:  K Sekiya; H Danbara; K Yase; Y Futaesaku
Journal:  J Bacteriol       Date:  1996-12       Impact factor: 3.490

4.  Use of a monoclonal antibody to determine the mode of transmembrane pore formation by streptolysin O.

Authors:  F Hugo; J Reichwein; M Arvand; S Krämer; S Bhakdi
Journal:  Infect Immun       Date:  1986-12       Impact factor: 3.441

5.  Nucleotide sequence of the gene for perfringolysin O (theta-toxin) from Clostridium perfringens: significant homology with the genes for streptolysin O and pneumolysin.

Authors:  R K Tweten
Journal:  Infect Immun       Date:  1988-12       Impact factor: 3.441

6.  Binding, oligomerization, and pore formation by streptolysin O in erythrocytes and fibroblast membranes: detection of nonlytic polymers.

Authors:  I Walev; M Palmer; A Valeva; U Weller; S Bhakdi
Journal:  Infect Immun       Date:  1995-04       Impact factor: 3.441

7.  Mechanism of membrane damage by streptolysin-O.

Authors:  S Bhakdi; J Tranum-Jensen; A Sziegoleit
Journal:  Infect Immun       Date:  1985-01       Impact factor: 3.441

8.  Mechanism of tetanolysin-induced membrane damage: studies with black lipid membranes.

Authors:  R Blumenthal; W H Habig
Journal:  J Bacteriol       Date:  1984-01       Impact factor: 3.490

9.  Binding of cholesterol by sulfhydryl-activated cytolysins.

Authors:  M K Johnson; C Geoffroy; J E Alouf
Journal:  Infect Immun       Date:  1980-01       Impact factor: 3.441

10.  Increased resistance to streptolysin O in mammalian cells treated with oxygenated derivatives of cholesterol.

Authors:  J L Duncan; L Buckingham
Journal:  Infect Immun       Date:  1978-10       Impact factor: 3.441

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