Literature DB >> 1697105

Pore-forming toxins: experiments with S. aureus alpha-toxin, C. perfringens theta-toxin and E. coli haemolysin in lipid bilayers, liposomes and intact cells.

G Menestrina1, C L Bashford, C A Pasternak.   

Abstract

Three quite different bacterial toxins (S. aureus alpha-toxin, C. perfringens theta-toxin and E. coli haemolysin) induce the leakage of phosphorylated metabolites from Lettre cells and of calcein from liposomes; in each case leakage is inhibited by Zn2+ greater than Ca2+ greater than Mg2+. Inhibition is not due to displacement of toxin from the membrane, since divalent cations inhibit leakage through pre-formed pores. Electrical conductivity across phospholipid bilayers is induced by each of the three toxins; in each case the probability of channels being in the open state is reduced by divalent cations. Although the pores induced in phospholipid bilayers and liposomes vary greatly in size (theta-toxin much greater than haemolysin greater than alpha-toxin), in Lettre cells the lesions appear more uniform, suggestive of a limiting effect in cells.

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Year:  1990        PMID: 1697105     DOI: 10.1016/0041-0101(90)90292-f

Source DB:  PubMed          Journal:  Toxicon        ISSN: 0041-0101            Impact factor:   3.033


  20 in total

1.  Differential sensitivity of pneumolysin-induced channels to gating by divalent cations.

Authors:  Y E Korchev; C L Bashford; C A Pasternak
Journal:  J Membr Biol       Date:  1992-05       Impact factor: 1.843

2.  Action of diphtheria toxin does not depend on the induction of large, stable pores across biological membranes.

Authors:  G M Alder; C L Bashford; C A Pasternak
Journal:  J Membr Biol       Date:  1990-01       Impact factor: 1.843

3.  Clostridium perfringens beta-toxin forms potential-dependent, cation-selective channels in lipid bilayers.

Authors:  O Shatursky; R Bayles; M Rogers; B H Jost; J G Songer; R K Tweten
Journal:  Infect Immun       Date:  2000-10       Impact factor: 3.441

4.  Triton channels are sensitive to divalent cations and protons.

Authors:  T K Rostovtseva; C L Bashford; A A Lev; C A Pasternak
Journal:  J Membr Biol       Date:  1994-07       Impact factor: 1.843

5.  Biological relevance of natural alpha-toxin fragments from Staphylococcus aureus.

Authors:  Young-Keun Kwak; Martin Högbom; Patricia Colque-Navarro; Roland Möllby; Beatrix Vécsey-Semjén
Journal:  J Membr Biol       Date:  2010-02-14       Impact factor: 1.843

6.  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

7.  Prelytic and lytic conformations of erythrocyte-associated Escherichia coli hemolysin.

Authors:  M Moayeri; R A Welch
Journal:  Infect Immun       Date:  1997-06       Impact factor: 3.441

Review 8.  Effects of MACPF/CDC proteins on lipid membranes.

Authors:  Robert J C Gilbert; Miha Mikelj; Mauro Dalla Serra; Christopher J Froelich; Gregor Anderluh
Journal:  Cell Mol Life Sci       Date:  2012-09-15       Impact factor: 9.261

Review 9.  Obstructing toxin pathways by targeted pore blockage.

Authors:  Ekaterina M Nestorovich; Sergey M Bezrukov
Journal:  Chem Rev       Date:  2012-10-11       Impact factor: 60.622

10.  Purification and analysis of a phospholipase A2-like lytic factor of Trichomonas vaginalis.

Authors:  Kirk J Lubick; Donald E Burgess
Journal:  Infect Immun       Date:  2004-03       Impact factor: 3.441

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