化学
乙二醇
共轭体系
表位
PEG比率
抗体
小分子
分子
组合化学
生物化学
有机化学
聚合物
财务
生物
经济
免疫学
作者
Chiao-Yu Hsiao,Jun-Lun Meng,Jung-Zhe Hong,Xuan-Huong Ly,Meng-Hsuan Lin,Chin‐Yuan Chang,Minh-Tram T. Nguyen,Tian-Lu Cheng,Wen-Wei Lin,Pierre‐Alain Burnouf,Talal Salem Al-Qaisi,En-Shuo Liu,Yu-Cheng Su
标识
DOI:10.1021/acs.bioconjchem.2c00416
摘要
Sensitive quantification of methoxy poly(ethylene glycol) (mPEG)-conjugated therapeutics for pharmacokinetic determination is critical for mPEGylated drug development. However, sensitive measurement of low-molecular-weight (lmw) mPEG compounds remains challenging due to epitope competition between backbone-specific anti-PEG antibodies. Here, we engineered a high-affinity methoxy-specific anti-mPEG antibody for sensitive quantification of free mPEG molecules and mPEGylated therapeutics. The affinity-enhanced h15-2Y antibody variant shows a 10.3-fold increase in mPEG-binding activity compared to parental h15-2b. h15-2Y-based sandwich ELISA can effectively quantify lmw mPEG5K and high-molecular-weight (hmw) mPEG20K at concentrations as low as 3.4 and 5.1 ng mL–1, respectively. Moreover, lmw mPEG compounds (560, 750, 1000, and 2000 Da) can be efficiently quantified via h15-2Y-based competitive ELISA with detection limits at nanomolar levels. This study provides a promising approach for application in the quantitative analysis of the various sizes of mPEG molecules to accelerate the timeline of mPEG-conjugated drug development.
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