Premium
A non‐toxic enzyme‐linked immunosorbent assay for aflatoxin B 1 using anti‐idiotypic antibodies as substitutes
Author(s) -
Hu Li,
Liu Aiping,
Chen Weifeng,
Yang Hongxiu,
Wang Xiaohong,
Chen Fusheng
Publication year - 2016
Publication title -
journal of the science of food and agriculture
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.782
H-Index - 142
eISSN - 1097-0010
pISSN - 0022-5142
DOI - 10.1002/jsfa.7914
Subject(s) - immunogen , aflatoxin , antigen , antibody , monoclonal antibody , chemistry , biology , food science , immunology
BACKGROUND Immunoassays are widely employed techniques to detect aflatoxins since they are rapid, selective and sensitive. One common disadvantage of them is using aflatoxins as standard substances, which may trigger exposure risks to operators and environmental contamination without proper handling. Anti‐idiotypic antibodies (anti‐Ids or Ab2s), also named as internal‐image anti‐Ids, are able to mimic and function as antigens, so a non‐toxic enzyme‐linked immunosorbent assay ( ELISA ) for aflatoxin B 1 ( AFB 1 ) is developed and validated using anti‐Ids as substitutes. RESULTS Mouse monoclonal anti‐idiotypic antibody ( McAb2 ) to AFB 1 was generated by the hybridoma technique using Fab fragments of rabbit anti‐ AFB 1 idiotype antibody (Ab1) as immunogen. As indicated by indirect competitive ELISA , McAb2 , represented an internal‐image of antigen AFB 1 , was able to bind Fab with competition to AFB 1 . Then, analysis of AFB 1 in spiked samples by non‐toxic ELISA using anti‐Ids as substitutes was developed, and it showed no significant differences with comparison to AFB 1 as competitive antigens. CONCLUSION Our work demonstrated that anti‐Ids could be used as internal‐image mimicry of AFB 1 , and it had potential applications in immunoassays for antigen substitution to reduce operational risk for operators and environmental contamination. © 2016 Society of Chemical Industry