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Detection of Cholesterol in Cell Membranes by Use of Bacterial Toxins

Overview
Journal J Bacteriol
Specialty Microbiology
Date 1972 May 1
PMID 4623312
Citations 2
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Abstract

A method is described for the detection of cholesterol in membranes from erythrocytes, mycoplasmas, and bacterial cells by a ferritin-labeling technique. Membranes treated with cereolysin, a bacterial hemolysin which specifically binds to cholesterol, and then treated with ferritin-antitetanolysin, were specifically ferritin-labeled for cholesterol. A similar antigen-antibody system, streptolysin O-ferritin-antistreptolysin, was also used successfully with erythrocyte membranes. There was an uneven distribution of ferritin in erythrocyte membranes suggesting that the distribution of cholesterol may not be entirely random. Mycoplasma gallisepticum was intensely labeled, but Acholeplasma laidlawii with or without cholesterol in the membranes was not labeled, suggesting an unusual location for cholesterol in A. laidlawii membranes. As controls, two of three species of bacterial membranes lacking cholesterol were not ferritin-labeled.

Citing Articles

Evidence for membrane cholesterol as the common binding site for cereolysin, streptolysin O and saponin.

Shany S, BERNHEIMER A, Grushoff P, Kim K Mol Cell Biochem. 1974; 3(3):179-86.

PMID: 4209248 DOI: 10.1007/BF01686643.


Purification of cereolysin and the electrophoretic separation of the active (reduced) and inactive (oxidized) forms of the purified toxin.

Cowell J, BERNHEIMER A Infect Immun. 1976; 14(1):144-54.

PMID: 820638 PMC: 420857. DOI: 10.1128/iai.14.1.144-154.1976.

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