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Engineering a High-Affinity Anti-Methoxy Poly(ethylene glycol) (mPEG) Antibody for Sensitive Immunosensing of mPEGylated Therapeutics and mPEG Molecules.

Chiao-Yu HsiaoJun-Lun MengJung-Zhe HongXuan-Huong LyMeng-Hsuan LinChin-Yuan ChangMinh-Tram T NguyenTian-Lu ChengWen-Wei LinPierre-Alain BurnoufTalal Salem Al-QaisiEn-Shuo LiuYu-Cheng Su
Published in: Bioconjugate chemistry (2022)
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 mPEG 5K and high-molecular-weight (hmw) mPEG 20K 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.
Keyphrases
  • small molecule
  • photodynamic therapy
  • drug delivery