A strategy for inducing an immune response against Androctonus australis scorpion venom toxin I in mice. Production of high-affinity monoclonal antibodies and their use in a sensitive two-site immunometric assay

J Immunol Methods. 2002 Dec 20;271(1-2):37-46. doi: 10.1016/s0022-1759(02)00338-1.

Abstract

Scorpion neurotoxins acting on ion channels share some structural features but differ in antigenic and immunogenic properties. They are highly structured peptides, 60-70 amino acids long. Monoclonal antibodies have been obtained for Androctonus australis hector scorpion venom neurotoxin II (AahII) and a nontoxic synthetic analog ((Abu)(8) AahII). In this study, no antibody response was elicited in mice of various strains injected with AahI, the other important toxin of the venom, in a native or an inactive ((Abu)(8) AahI) form. We found that AahI was only immunogenic in BALB/c or C57BL/6 mice if it was coupled to a carrier protein. The helper protein molecule could be BSA, KLH, or the nontoxic analog of AahII. We obtained a panel of high-affinity mAbs with these immunogens. Two of these mAbs, including the very high-affinity antibody 9C2 (K(D)=0.11x10(-11) M), were used to set up a two-site ELISA, sensitive enough for the quantification of AahI in the biological fluids of envenomed animals. The detection limit of the assay was 75 pg/ml.

MeSH terms

  • Animals
  • Antibodies, Monoclonal / biosynthesis
  • Antibodies, Monoclonal / immunology*
  • Antivenins / immunology
  • Carrier Proteins / immunology
  • Enzyme-Linked Immunosorbent Assay / methods*
  • Immunoglobulin G / analysis
  • Male
  • Mice
  • Mice, Inbred BALB C
  • Mice, Inbred C57BL
  • Neurotoxins / immunology*
  • Rabbits
  • Radioimmunoassay / methods*
  • Scorpion Venoms / immunology*
  • Scorpions / immunology*
  • Surface Plasmon Resonance

Substances

  • Antibodies, Monoclonal
  • Antivenins
  • Carrier Proteins
  • Immunoglobulin G
  • Neurotoxins
  • Scorpion Venoms
  • scorpion toxin I, Androctonus