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A Recombinant Insect-Specific alpha-Toxin of Buthus occitanus tunetanus Scorpion Confers Protection Against Homologous Mammal Toxins

Authors :
Habib Karoui
Mohamed El Ayeb
Balkiss Bouhaouala-Zahar
Lamia Borchani
I. Zenouaki
M. Pelhate
André Ménez
Frédérique Ducancel
Rym Ben Khalifa
J.-C. Boulain
Laboratoire des Venins et Toxines, Institut Pasteur de Tunis
Institut Pasteur de Tunis
Réseau International des Instituts Pasteur (RIIP)-Réseau International des Instituts Pasteur (RIIP)
Département d'Ingénierie et d'Etudes des Protéines
Commissariat à l'énergie atomique et aux énergies alternatives (CEA)
Laboratoire de Neurophysiologie
Centre National de la Recherche Scientifique (CNRS)
This research was supported by the Institut National de la Sante et de la Recherche Medicale grant no. 492 NS6
Source :
European Journal of Biochemistry, European Journal of Biochemistry, 1996, 238 (3), pp.653-660. ⟨10.1111/j.1432-1033.1996.0653w.x⟩
Publication Year :
1996
Publisher :
Wiley, 1996.

Abstract

International audience; We have constructed a cDNA library from venom glands of the scorpion Buthus occitanus tunetanus and cloned a DNA sequence that encodes an alpha-toxin. This clone was efficiently expressed in Escherichia coli as a fusion protein with two Ig-binding (Z) domains of protein A from Staphylococcus aureus. After CNBr treatment of the fusion protein and HPLC purification, we obtained approximately 1 mg recombinant apha-toxin/l bacterial culture. The toxin, called Bot XIV, displays no toxicity towards mammals but is active towards insects as shown by its paralytic activity against Blatella germanica cockroach and by electrophysiological studies on Periplaneta americana cockroaches. The Bot XIV protein fused to two Z domains is highly immunogenic in mice and induces production of antisera that specifically recognize and neutralize highly toxic components that had been injected into mice. This fusion protein could be very useful for development of potent protective antisera against scorpion venoms.

Details

ISSN :
14321033, 00142956, and 14321327
Volume :
238
Database :
OpenAIRE
Journal :
European Journal of Biochemistry
Accession number :
edsair.doi.dedup.....abcd192c1d72c331a1c943d538e20b44