Premium
Immunodetection and immunopurification of aflatoxins using a high affinity monoclonal antibody to aflatoxin B1
Author(s) -
KAVERI S. V.,
FREMY JM.,
LAPEYRE C.,
STROSBERG A. D.
Publication year - 1987
Publication title -
letters in applied microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.698
H-Index - 110
eISSN - 1472-765X
pISSN - 0266-8254
DOI - 10.1111/j.1472-765x.1987.tb01586.x
Subject(s) - aflatoxin , monoclonal antibody , antibody , chemistry , chromatography , bovine serum albumin , biochemistry , microbiology and biotechnology , biology , food science , immunology
A monoclonal antibody was obtained from BALB/c mice immunized with aflatoxin Bl (AFB1) conjugated to bovine serum albumin. This IgG2a antibody, ASCI, with K light chain has a high specificity for AFB1. In an indirect enzyme‐linked immunosorbent assay the antibody litre in ascites fluid was 1: 6000 for 50% binding to plates coated with aflatoxin‐poly‐L‐lysine. The assay is sensitive to 2.5 pg aflatoxin/assay. ASCI cross‐reacts with closely related aflatoxin metabolites such as AFB2, AFM1 and AFG1. However, ASCI displays negligible cross‐reactivity with other related aflatoxin analogues such as AFM2, AFP1, AFQ1 and aflatoxicol. An immunoabsorbent was prepared by coupling ASCI antibody to Ultrogel AcA 22. This immunomatrix was used to purify aflatoxins at 0–1 ng/ml levels from contaminated body fluids such as bovine milk. The antibody affinity column was regenerated and re‐used several times. Owing to its high specificity for AFB1 and AFM1, ASCI will be of value in immunodetection and immunopurification of these toxins in various foodstuffs.