Literature DB >> 3818590

Interaction of the alpha-toxin of Staphylococcus aureus with the liposome membrane.

H Ikigai, T Nakae.   

Abstract

When the liposome membrane is exposed to the alpha-toxin of Staphylococcus aureus, fluorescence of the tryptophan residue(s) of the toxin molecule increases concomitantly with the degree of toxin-hexamer formation (Ikigai, H., and Nakae, T. (1985) Biochem. Biophys. Res. Commun. 130, 175-181). In the present study, the toxin-membrane interaction was distinguished from the hexamer formation by the fluorescence energy transfer from the tryptophan residue(s) of the toxin molecule to the dansylated phosphatidylethanolamine in phosphatidylcholine liposome. Measurement of these two parameters yielded the following results. The effect of the toxin concentration and phospholipid concentration on these two parameters showed first order kinetics. The effect of liposome size on the energy transfer and the fluorescence increment of the tryptophan residue(s) was only detectable in small liposomes. Under moderately acidic or basic conditions, the fluorescence energy transfer always preceded the fluorescence increment of the tryptophan residue(s). The fluorescence increment at 336 nm at temperatures below 20 degrees C showed a latent period, whereas the fluorescence energy transfer did not. These results were thought to indicate that when alpha-toxin damages the target membrane, the molecule interacts with the membrane first, and then undergoes oligomerization within the membrane.

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Year:  1987        PMID: 3818590

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  7 in total

1.  Channel-forming abilities of spontaneously occurring alpha-toxin fragments from Staphylococcus aureus.

Authors:  Beatrix Vécsey-Semjén; Young-Keun Kwak; Martin Högbom; Roland Möllby
Journal:  J Membr Biol       Date:  2010-03-26       Impact factor: 1.843

2.  Staphylococcal alpha-toxin kills human keratinocytes by permeabilizing the plasma membrane for monovalent ions.

Authors:  I Walev; E Martin; D Jonas; M Mohamadzadeh; W Müller-Klieser; L Kunz; S Bhakdi
Journal:  Infect Immun       Date:  1993-12       Impact factor: 3.441

Review 3.  A guide to the use of pore-forming toxins for controlled permeabilization of cell membranes.

Authors:  S Bhakdi; U Weller; I Walev; E Martin; D Jonas; M Palmer
Journal:  Med Microbiol Immunol       Date:  1993-09       Impact factor: 3.402

4.  Histidine residues near the N terminus of staphylococcal alpha-toxin as reporters of regions that are critical for oligomerization and pore formation.

Authors:  R Jursch; A Hildebrand; G Hobom; J Tranum-Jensen; R Ward; M Kehoe; S Bhakdi
Journal:  Infect Immun       Date:  1994-06       Impact factor: 3.441

Review 5.  Alpha-toxin of Staphylococcus aureus.

Authors:  S Bhakdi; J Tranum-Jensen
Journal:  Microbiol Rev       Date:  1991-12

6.  Novel path to apoptosis: small transmembrane pores created by staphylococcal alpha-toxin in T lymphocytes evoke internucleosomal DNA degradation.

Authors:  D Jonas; I Walev; T Berger; M Liebetrau; M Palmer; S Bhakdi
Journal:  Infect Immun       Date:  1994-04       Impact factor: 3.441

Review 7.  Staphylococcus aureus α-toxin: nearly a century of intrigue.

Authors:  Bryan J Berube; Juliane Bubeck Wardenburg
Journal:  Toxins (Basel)       Date:  2013-06       Impact factor: 4.546

  7 in total

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