TY - JOUR
T1 - Engineering a High-Affinity Anti-Methoxy Poly(ethylene glycol) (mPEG) Antibody for Sensitive Immunosensing of mPEGylated Therapeutics and mPEG Molecules
AU - Hsiao, Chiao Yu
AU - Meng, Jun Lun
AU - Hong, Jung Zhe
AU - Ly, Xuan Huong
AU - Lin, Meng Hsuan
AU - Chang, Chin Yuan
AU - Nguyen, Minh Tram T.
AU - Cheng, Tian Lu
AU - Lin, Wen Wei
AU - Burnouf, Pierre Alain
AU - Al-Qaisi, Talal Salem
AU - Liu, En Shuo
AU - Su, Yu Cheng
N1 - Publisher Copyright:
© 2022 American Chemical Society. All rights reserved.
PY - 2022/11/16
Y1 - 2022/11/16
N2 - 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 mPEG5Kand high-molecular-weight (hmw) mPEG20Kat 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.
AB - 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 mPEG5Kand high-molecular-weight (hmw) mPEG20Kat 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.
UR - http://www.scopus.com/inward/record.url?scp=85141640265&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85141640265&partnerID=8YFLogxK
U2 - 10.1021/acs.bioconjchem.2c00416
DO - 10.1021/acs.bioconjchem.2c00416
M3 - Article
C2 - 36320124
AN - SCOPUS:85141640265
SN - 1043-1802
VL - 33
SP - 2180
EP - 2188
JO - Bioconjugate Chemistry
JF - Bioconjugate Chemistry
IS - 11
ER -