Work

Synthesis and characterization of a functional benzoylecgonine – bovine serum albumin conjugate for quantification of a humanized monoclonal anti-cocaine antibody

Year: 2025

Type: article

Abstract: We have developed a humanized monoclonal anti-cocaine antibody (h2E2), as a potential solution for cocaine use disorder. A key milestone was the development of an assay to quantify this monoclonal antibody (mAb) in animal and human blood. Thus, we synthesized a novel benzoylecgonine-1,4-diaminobutane-BSA (BE-diab BSA) conjugate as an antigen for quantifying h2E2 using ELISA. We report here the method of synthesis of this conjugate, BE-diab BSA, and assessment of its binding to the h2E2 mAb using an ELISA and a fluorescence quenching assay. Compared with four commercial BE-BSA conjugates, BE-diab BSA demonstrated markedly stronger mAb binding in ELISA—three of the commercial conjugates showed less than 10 % relative binding. Fluorescence quenching assays confirmed this binding superiority, with the commercial conjugates showing minimal mAb interaction, while BE-diab BSA induced robust intrinsic fluorescence quenching. SDS-PAGE analyses identified structural differences consistent with binding results between our functional conjugate and the commercial preparations. This functional and reproducible in-house conjugation has been integrated into a GLP-validated ELISA, which is now in use for pharmacokinetic analyses and for qualifying antibody release lots for clinical deployment. • Several commercial BE-BSA conjugates were found to be unsuitable for ELISA h2E2 mAb quantitation . • A novel, spacer-linked benzoylecgonine-BSA conjugate synthesized and characterized . • Rapid and simple fluorescence quenching assay developed to test the BE-BSA conjugate . • Successful and reproducible ELISA quantitation of h2E2 mAb using the BE-BSA conjugate . • External GLP lab used the conjugate successfully in h2E2 anti-cocaine mAb release assay .

Source: Biochemistry and Biophysics Reports

DOI: 10.1016/j.bbrep.2025.102282

Authors: Rose P. Webster, Terence L. Kirley, Andrew R. Ray, Zhen-Hin Chan, Andrew B. Norman

Institution: University of Cincinnati

Language: English

Topic: Monoclonal and Polyclonal Antibodies Research

Subfield: Radiology, Nuclear Medicine and Imaging

Field: Medicine

Domain: Health Sciences

SDG: Good health and well-being

Open Access status: gold

Estimated APC paid: $2,700