Production of antibodies that bind biotin and inhibit biotin containing enzymes
- 1 June 1975
- journal article
- Published by American Chemical Society (ACS) in Biochemistry
- Vol. 14 (11) , 2338-2342
- https://doi.org/10.1021/bi00682a010
Abstract
Methods were developed for the coupling of biotin to bovine serum albumin and bovine gamma-globulin using a water-soluble carbodimide. The use of [14-C]biotin as a tracer allowed quantitation of the incorporation of biotin into the conjugates: 2.55 mol of biotin was incorporated per mol of gamma-globulin and 7-9 mol of biotin was incorporated per mol of serum albumin in different preparations. These conjugates were highly immunogenic in the rabbit and anti-bodies reactive with the biotinyl group itself could be detected by their ability to precipitate the heterologous biotinated carrier but not the unmodified heterologous carrier. There antisera rapidly inactivated transcarboxylase and pyruvate carboxylase and this inactivation could be blocked by pretreatment of the antisera with biotin or biocytin. Using enzyme inhibition to detect free antibody, the binding constant for biotin was found to be 5.0 x 10- minus 8 M and that for biocytin 3.5 x 10- minus 8 M.Keywords
This publication has 5 references indexed in Scilit:
- Inactivation of staphylococcal nuclease by the binding of antibodies to a distinct antigenic determinantBiochemistry, 1972
- TranscarboxylasePublished by Elsevier ,1972
- [38] Pyruvate carboxylase from chicken liverPublished by Elsevier ,1969
- [36] Oxaloacetate transcarboxylase from PropionibacteriumPublished by Elsevier ,1969
- Relaxation Spectrometry of Biological SystemsPublished by Elsevier ,1968