半抗原
单克隆抗体
结合
抗体
芬太尼
免疫
免疫系统
小分子
药理学
化学
免疫学
生物
生物化学
数学
数学分析
作者
Asheley P. Chapman,Minghao Xu,Michelle Schroeder,Jason Goldstein,Asiya Seema Chida,Joo R. Lee,Xiaoling Tang,Rebekah E. Wharton,M. G. Finn
出处
期刊:ACS Nano
[American Chemical Society]
日期:2025-01-10
标识
DOI:10.1021/acsnano.4c14369
摘要
Structural variants of the synthetic opioid fentanyl are a major threat to public health. Following an investigation showing that many derivatives are poorly detected by commercial lateral flow and related assays, we created hapten conjugate vaccines using an immunogenic virus-like particle carrier and eight synthetic fentanyl derivatives designed to mimic the structural features of several of the more dangerous analogues. Immunization of mice elicited strong antihapten humoral responses, allowing the screening of hundreds of hapten-specific hybridomas for binding strength and specificity. A panel of 13 monoclonal IgG antibodies were selected, each showing a different pattern of recognition of fentanyl structural variations, and all proving to be highly efficient at capturing parent fentanyl compounds in competition ELISA experiments. These results provide antibody reagents for assay development as well as a demonstration of the power of the immune system to create binding agents capable of both broad and specific recognition of small-molecule targets.
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