Development of protective agent against Hottentotta saulcyi venom using camelid single-domain antibody

被引:16
|
作者
Darvish, Maryam [1 ]
Behdani, Mahdi [1 ]
Shokrgozar, Mohammad Ali [2 ]
Pooshang-Bagheri, Kamran [1 ]
Shahbazzadeh, Delavar [1 ]
机构
[1] Pasteur Inst Iran, Biotechnol Res Ctr, Venom & Biotherapeut Mol Lab, Tehran, Iran
[2] Pasteur Inst Iran, Natl Cell Bank Iran, Tehran, Iran
关键词
Hottentotta saulcyi; Nanobody; Phage display; Heavy chain antibody (HC-Ab); Antivenom; PHAGE DISPLAY; NEUTRALIZATION; IDENTIFICATION; SCORPIONISM; ANTIVENOM; FRAGMENTS; AFFINITY; NANOBODY; IRAN;
D O I
10.1016/j.molimm.2015.10.002
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Hottentotta saulcyi, medically important scorpion species, causes some of harmful toxic exposure in Iran. Administrated, conventional antivenom-based immunotherapy is still limited and hardly meet ideal characteristic of effective treatment for scorpion envenomation. In this study we aimed to develop a neutralizing agent directed against scorpion venom based on VHH, variable domain of the Camelidae heavy chain antibody or Nanobody. This promising biomolecule is well-established as an advantageous tool for therapeutic purposes due to its small size, stability, monomeric performance and less immunogenicity. In this study, a large Nb library was constructed and phage displayed after successful camel immunization using H. saulcyi scorpion crude venom. After a series of biopanning rounds on Sephadex G50 purified venom fraction and screening by monoclonal phage ELISA, the best reactive Nb was retrieved and designated Nb12. The selected Nb was then expressed as soluble protein in Escherichia coli, purified and confirmed by SOS-PAGE analysis and western blotting. The lead candidate Nb12 bound scorpion venom with Kaff value of 5 x 10(7) M-1. Nb12 was shown to be capable of neutralizing 2 LD50 of whole venom of scorpion toxin when injected in the ratio of the Nb/toxin of 1.4:1 into C57BL/6 mice. In challenge experiment, Nb succeeded to rescue all i.p. lethal dose injected mice even when administrated i.v., 20 min after envenoming. These results with ease of production and superior neutralizing activity make Nb a suitable anti-toxin candidate for treatment of scorpion envenoming. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:412 / 420
页数:9
相关论文
共 50 条
  • [1] Camelid antivenom development and potential in vivo neutralization of Hottentotta saulcyi scorpion venom
    Darvish, Maryam
    Ebrahimi, Soltan Ahmad
    Shahbazzadeh, Delavar
    Bagheri, Kamran-Pooshang
    Behdani, Mandi
    Shokrgozar, Mohammad Ali
    TOXICON, 2016, 113 : 70 - 75
  • [2] Properties, production, and applications of camelid single-domain antibody fragments
    M. M. Harmsen
    H. J. De Haard
    Applied Microbiology and Biotechnology, 2007, 77 : 13 - 22
  • [3] Properties, production, and applications of camelid single-domain antibody fragments
    Harmsen, M. M.
    De Haard, H. J.
    APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2007, 77 (01) : 13 - 22
  • [4] Structure and Properties of a Complex of α-Synuclein and a Single-Domain Camelid Antibody
    De Genst, Erwin J.
    Guilliams, Tim
    Wellens, Joke
    O'Day, Elizabeth M.
    Waudby, Christopher A.
    Meehan, Sarah
    Dumoulin, Mireille
    Hsu, Shang-Te Danny
    Cremades, Nunilo
    Verschueren, Koen H. G.
    Pardon, Els
    Wyns, Lode
    Steyaert, Jan
    Christodoulou, John
    Dobson, Christopher M.
    JOURNAL OF MOLECULAR BIOLOGY, 2010, 402 (02) : 326 - 343
  • [5] Thermodynamic and structural studies of camelid single-domain antibody binding to methotrexate
    Schmitt, Allison A.
    Mosley, Pamela
    Dunham, Jasmine N.
    Robbins, Hilary
    Toone, Eric J.
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2011, 242
  • [6] Hapten-Induced Dimerization of a Single-Domain VHH Camelid Antibody
    Sonneson, Gregory J.
    Horn, James R.
    BIOCHEMISTRY, 2009, 48 (29) : 6693 - 6695
  • [7] Development and characterization of a camelid single-domain antibody directed to human CD22 biomarker
    Faraji, Fatemeh
    Tajik, Nader
    Behdani, Mahdi
    Shokrgozar, Mohammad Ali
    Zarnani, Amir Hassan
    Shahhosseini, Fatemeh
    Habibi-Anbouhi, Mahdi
    BIOTECHNOLOGY AND APPLIED BIOCHEMISTRY, 2018, 65 (05) : 718 - 725
  • [8] Camelid Single-Domain Antibodies for the Development of Potent Diagnosis Platforms
    Brilhante-da-Silva, Nairo
    de Oliveira Sousa, Rosa Maria
    Arruda, Andrelisse
    dos Santos, Eliza Lima
    Marinho, Anna Carolina Machado
    Stabeli, Rodrigo Guerino
    Fernandes, Carla Freire Celedonio
    Pereira, Soraya dos Santos
    MOLECULAR DIAGNOSIS & THERAPY, 2021, 25 (04) : 439 - 456
  • [9] Camelid Single-Domain Antibodies for the Development of Potent Diagnosis Platforms
    Nairo Brilhante-da-Silva
    Rosa Maria de Oliveira Sousa
    Andrelisse Arruda
    Eliza Lima dos Santos
    Anna Carolina Machado Marinho
    Rodrigo Guerino Stabeli
    Carla Freire Celedonio Fernandes
    Soraya dos Santos Pereira
    Molecular Diagnosis & Therapy, 2021, 25 : 439 - 456
  • [10] Inhibition of the Myotoxicity Induced by Bothrops jararacussu Venom and Isolated Phospholipases A2 by Specific Camelid Single-Domain Antibody Fragments
    Prado, Nidiane D. R.
    Pereira, Soraya S.
    da Silva, Michele P.
    Morais, Michelle S. S.
    Kayano, Anderson M.
    Moreira-Dill, Leandro S.
    Luiz, Marcos B.
    Zanchi, Fernando B.
    Fuly, Andre L.
    Huacca, Maribel E. F.
    Fernandes, Cleberson F.
    Calderon, Leonardo A.
    Zuliani, Juliana P.
    Pereira da Silva, Luiz H.
    Soares, Andreimar M.
    Stabeli, Rodrigo G.
    Fernandes, Carla F. C.
    PLOS ONE, 2016, 11 (03):