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Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components

Schwartz, J.-L., Potvin, L., Coux, F., Charles, J.-F., Berry, Colin, Humphreys, M. J., Jones, A. F., Bernhart, I., Dalla Serra, M. and Menestrina, G. 2001. Permeabilization of model lipid membranes by Bacillus sphaericus mosquitocidal binary toxin and its individual components. Journal of Membrane Biology 184 (2) , pp. 171-183. 10.1007/s00232-001-0086-1

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Abstract

The high larvicidal effect of Bacillus sphaericus (Bs), a mosquito control agent, originates from the presence of a binary toxin (Bs Bin) composed of two proteins (BinA and BinB) that work together to lyse gut cells of susceptible larvae. We demonstrate for the first time that the binary toxin and its individual components permeabilize receptor-free large unilamellar phospholipid vesicles (LUVs) and planar lipid bilayers (PLBs) by a mechanism of pore formation. Calcein-release experiments showed that LUV permeabilization was optimally achieved at alkaline pH and in the presence of acidic lipids. BinA was more efficient than BinB, BinB facilitated the BinA effect, and their stoichiometric mixture was more effective than the full Bin toxin. In PLBs, BinA formed voltage-dependent channels of ≈100–200 pS with long open times and a high open probability. Larger channels (≥400 pS) were also observed. BinB, which inserted less easily, formed smaller channels (≤100 pS) with shorter mean open times. Channels observed after sequential addition of the two components, or formed by their 1:1 mixture (w/w), displayed BinA-like activity. Bs Bin toxin was less efficient at forming channels than the BinA/BinB mixture, with channels displaying the BinA channel behavior. Our data support the concept of BinA being principally responsible for pore formation in lipid membranes with BinB, the binding component of the toxin, playing a role in promoting channel activity.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Biosciences
Publisher: Springer US
ISSN: 0022-2631
Last Modified: 04 Jun 2017 06:44
URI: http://orca.cf.ac.uk/id/eprint/64308

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