Scorpion venom, containing highly toxic, small polypeptides that diffuse rapidly within the patient, causes serious medical problems. Nanobodies, single-domain antigen-binding fragments derived from dromedary heavy-chain antibodies, have a size that closely matches that of scorpion toxins. Therefore these nanobodies might be developed into potent immunotherapeutics to treat scorpion envenoming. Multiple nanobodies of sub-nanomolar affinity to AahII, the most toxic polypeptide within the Androctonus australis hector venom, were isolated from a dromedary immunized with AahII. These nanobodies neutralize the lethal effect of AahII to various extents without clear correlation with the kinetic rate constants kon or koff, or the equilibrium dissociation constant, KD. One particular nanobody, referred to as NbAahII10, which targets a unique epitope on AahII, neutralizes 7 LD50 of this toxin in mice, corresponding to a neutralizing capacity of approx. 37000 LD50 of AahII/mg of nanobody. Such high neutralizing potency has never been reached before by any other monoclonal antibody fragment.
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December 2009
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Research Article|
November 11 2009
Identification of potent nanobodies to neutralize the most poisonous polypeptide from scorpion venom
Rahma Ben Abderrazek;
Rahma Ben Abderrazek
*Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, 13 Place Pasteur, BP-74, 1002 Tunis, Tunisia
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Issam Hmila;
Issam Hmila
*Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, 13 Place Pasteur, BP-74, 1002 Tunis, Tunisia
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Cécile Vincke;
Cécile Vincke
†Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium
‡Department of Cellular and Molecular Interactions, Vlaams Interuniversitair Instituut voor Biotechnologie (VIB), 1050 Brussels, Belgium
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Zakaria Benlasfar;
Zakaria Benlasfar
§Unité des services animaliers-Institut Pasteur de Tunis, 13 Place Pasteur, BP-74, 1002 Tunis, Tunisia
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Mireille Pellis;
Mireille Pellis
†Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium
‡Department of Cellular and Molecular Interactions, Vlaams Interuniversitair Instituut voor Biotechnologie (VIB), 1050 Brussels, Belgium
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Hafedh Dabbek;
Hafedh Dabbek
∥Centre régional de production animalière de Kébili, 4200 Kébili, Tunisia
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Dirk Saerens;
Dirk Saerens
†Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium
‡Department of Cellular and Molecular Interactions, Vlaams Interuniversitair Instituut voor Biotechnologie (VIB), 1050 Brussels, Belgium
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Mohamed El Ayeb;
Mohamed El Ayeb
*Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, 13 Place Pasteur, BP-74, 1002 Tunis, Tunisia
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Serge Muyldermans;
Serge Muyldermans
†Laboratory of Cellular and Molecular Immunology, Vrije Universiteit Brussel, Pleinlaan 2, 1050 Brussels, Belgium
‡Department of Cellular and Molecular Interactions, Vlaams Interuniversitair Instituut voor Biotechnologie (VIB), 1050 Brussels, Belgium
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Balkiss Bouhaouala-Zahar
Balkiss Bouhaouala-Zahar
1
*Laboratoire des Venins et Toxines, Institut Pasteur de Tunis, 13 Place Pasteur, BP-74, 1002 Tunis, Tunisia
¶Faculté de Médecine de Tunis, Université de Tunis-El Manar, Tunis Romana 1068, Tunis BP94, Tunisia
1To whom correspondence should be addressed (email [email protected]).
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Publisher: Portland Press Ltd
Received:
May 07 2009
Revision Received:
August 11 2009
Accepted:
September 04 2009
Accepted Manuscript online:
September 04 2009
Online ISSN: 1470-8728
Print ISSN: 0264-6021
© The Authors Journal compilation © 2009 Biochemical Society
2009
Biochem J (2009) 424 (2): 263–272.
Article history
Received:
May 07 2009
Revision Received:
August 11 2009
Accepted:
September 04 2009
Accepted Manuscript online:
September 04 2009
Citation
Rahma Ben Abderrazek, Issam Hmila, Cécile Vincke, Zakaria Benlasfar, Mireille Pellis, Hafedh Dabbek, Dirk Saerens, Mohamed El Ayeb, Serge Muyldermans, Balkiss Bouhaouala-Zahar; Identification of potent nanobodies to neutralize the most poisonous polypeptide from scorpion venom. Biochem J 1 December 2009; 424 (2): 263–272. doi: https://doi.org/10.1042/BJ20090697
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