Membrane Insertion of Escherichia coli α-Hemolysin Is Independent from Membrane Lysis

• Published in: The Journal of biological chemistry Vol. 281; no. 9; pp. 5461 - 5467
• Main Authors: Sánchez-Magraner, Lissete, Cortajarena, Aitziber L., Goñi, Félix M., Ostolaza, Helena
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 03.03.2006
• Subjects: Adsorption; Calcium - metabolism; Cell Membrane - metabolism; Escherichia coli; Escherichia coli - metabolism; Escherichia coli Proteins - genetics; Escherichia coli Proteins - metabolism; Hemolysin Proteins - genetics; Hemolysin Proteins - metabolism; Lipids - chemistry; Liposomes - chemistry; Liposomes - metabolism
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1074/jbc.M512897200

Escherichia coli α-hemolysin (HlyA) is a protein exotoxin that binds and lyses eukaryotic cell and model membranes in the presence of calcium. Previous studies have been able to distinguish between reversible toxin binding to the membrane and irreversible insertion into the lipid matrix. Membrane lysis occurs as the combined effect of protein insertion plus a transient perturbation of the membrane bilayer structure. In the past, insertion and bilayer perturbation have not been experimentally dissected. This has now been achieved by studying HlyA penetration into lipid monolayers at the air-water interface, in which three-dimensional effects (of the kind required to break down the bilayer permeability barrier) cannot occur. The study of native HlyA, together with the nonlytic precursor pro-HlyA, and of different mutants demonstrates that although some nonlytic variants (e.g. pro-HlyA) exhibit very low levels of insertion, others (e.g. the nonlytic mutant HlyA H859N) insert even more strongly than the lytic wild type. These results show that insertion does not necessarily lead to membrane lysis, i.e. that insertion and lysis are not “coupled” phenomena. Millimolar levels of Ca2+, which are essential for the lytic activity, cause an extra degree of insertion but only in the case of the lytic forms of HlyA.