6533b7dafe1ef96bd126e1f7

RESEARCH PRODUCT

Production and characterization of a monoclonal antibody to the trichothecene mycotoxin diacetoxyscirpenol.

Dieter Bitter-suermannKlaus DoseJosef Urban Pauly

subject

medicine.drug_classTrichotheceneEnzyme-Linked Immunosorbent AssayCross ReactionsMonoclonal antibodyBiochemistryDiacetoxyscirpenolchemistry.chemical_compoundMicemedicineAnimalsBovine serum albuminAntiserumMice Inbred BALB CbiologyAntibodies MonoclonalMycotoxinsMolecular biologyTiterchemistryMonoclonalbiology.proteinFemaleAntibodyTrichothecenesSesquiterpenes

description

A monoclonal antibody was obtained by the fusion of mouse myeloma cells with splenocytes isolated from Balb/c mice, which had been immunized with diacetoxyscirpenol-hemiglutarate (DAS-hemiglutarate) and verrucarol-hemiglutarates covalently bound to ethylenediamine-modified bovine serum albumin. The anti-DAS-antibody that could be induced was of the IgM type with kappa-chains. The titer of the monoclonal anti-DAS-antibody in ascites fluid obtained from mice injected the selected cell line was much higher than those of conventional antisera. An enzyme-linked immunosorbent assay based on the competitive binding principle in which the antibody was applied had a sensitivity of 1 ng DAS per assay. The relative cross-reactivity of the monoclonal antibody in the CI-ELISA with the related trichothecenes such as triacetoxyscirpenol, 15-monoacetoxyscirpenol, diacetylverrucarol, 4-monoacetoxyscirpenol and scirpentriol were found to be 1.8, 0.8, 0.15, 0.02 and less than 0.001, respectively. The trichothecenes verrucarol, T-2 toxin, T-2 tetraol, deoxynivalenol, 3-acetyldeoxynivalenol and trichothecin showed no cross-reactivity.

10.1515/bchm3.1988.369.1.487https://pubmed.ncbi.nlm.nih.gov/3202955