A Single C226S Mutation Rescues Fragmentation and Enhances Antigen-Binding Activity of a Giant Panda Chimeric Antibody Against Canine Distemper Virus

Background/Objectives: Canine distemper virus (CDV) poses a major threat to the conservation of the endangered giant panda (Ailuropoda melanoleuca). Although monoclonal antibodies hold great therapeutic promise, the development of species-specific antibody therapeutics for wildlife remains challenging. In this study, we aimed to construct and optimize a giant panda chimeric antibody targeting the CDV H protein through Fc engineering. Methods: A chimeric antibody (6G4-gpIgG1) was constructed by fusing the variable regions of a murine anti-CDV H antibody with giant panda IgG1b Fc. Structural analysis using AlphaFold identified excessive hinge exposure as a potential cause of instability. A C226S mutation in the hinge region was designed and introduced. The wild-type and mutant antibodies were expressed in CHO-S cells, purified, and characterized by SDS-PAGE, ELISA, biolayer interferometry (BLI), and SEC-HPLC. Results: The wild-type murine–giant panda chimeric antibody exhibited degradation fragmentation and a nanomolar-range binding affinity (EC50 = 0.62 nM; BLI KD = 4.27 × 10−9 M). The C226S mutation (6G4-gpIgG1-Opt2) reduced fragmentation, increased monomer purity from 88.38% to 96.99%, and increased antigen-binding activity by over 30-fold (EC50 = 0.019 nM), reaching levels comparable to the murine–canine chimeric control, which exhibited a canonical Y-shaped conformation. BLI also revealed stronger binding affinity for Opt2 (KD = 1.33 × 10−10 M), associated with a slower dissociation rate (kdis = 7.80 × 10−5 s−1 versus 1.15 × 10−3 s−1 for the wild type). Conclusions: A single C226S mutation in the giant panda IgG1 hinge region substantially improves structural stability, reducing degradation fragments, increasing monomer purity, and unexpectedly enhancing antigen-binding affinity by over 30-fold. This study provides a structure-guided Fc engineering strategy for developing chimeric antibodies in giant pandas, offering a promising candidate for CDV protection and a generalizable framework for conservation medicine.

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Journal
Antibodies
Published
2026-11-04
DOI
https://doi.org/10.3390/antib15060104
Primary Topic
Monoclonal and Polyclonal Antibodies Research
Type
article
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article

A Single C226S Mutation Rescues Fragmentation and Enhances Antigen-Binding Activity of a Giant Panda Chimeric Antibody Against Canine Distemper Virus

Qiaoli Lang, Chanjuan Yue, Songrui Liu, 苏晓艳 et al.
Antibodies
Monoclonal and Polyclonal Antibodies Research
article

A Single C226S Mutation Rescues Fragmentation and Enhances Antigen-Binding Activity of a Giant Panda Chimeric Antibody Against Canine Distemper Virus

Qiaoli Lang, Chanjuan Yue, Songrui Liu, 苏晓艳, Jianhong Zeng, Xi Yang, Wei Wang, Dongsheng Zhang, Yunli Li, Xia Yan, Hongwen Zhang
article en

Abstract

Background/Objectives: Canine distemper virus (CDV) poses a major threat to the conservation of the endangered giant panda (Ailuropoda melanoleuca). Although monoclonal antibodies hold great therapeutic promise, the development of species-specific antibody therapeutics for wildlife remains challenging. In this study, we aimed to construct and optimize a giant panda chimeric antibody targeting the CDV H protein through Fc engineering. Methods: A chimeric antibody (6G4-gpIgG1) was constructed by fusing the variable regions of a murine anti-CDV H antibody with giant panda IgG1b Fc. Structural analysis using AlphaFold identified excessive hinge exposure as a potential cause of instability. A C226S mutation in the hinge region was designed and introduced. The wild-type and mutant antibodies were expressed in CHO-S cells, purified, and characterized by SDS-PAGE, ELISA, biolayer interferometry (BLI), and SEC-HPLC. Results: The wild-type murine–giant panda chimeric antibody exhibited degradation fragmentation and a nanomolar-range binding affinity (EC50 = 0.62 nM; BLI KD = 4.27 × 10−9 M). The C226S mutation (6G4-gpIgG1-Opt2) reduced fragmentation, increased monomer purity from 88.38% to 96.99%, and increased antigen-binding activity by over 30-fold (EC50 = 0.019 nM), reaching levels comparable to the murine–canine chimeric control, which exhibited a canonical Y-shaped conformation. BLI also revealed stronger binding affinity for Opt2 (KD = 1.33 × 10−10 M), associated with a slower dissociation rate (kdis = 7.80 × 10−5 s−1 versus 1.15 × 10−3 s−1 for the wild type). Conclusions: A single C226S mutation in the giant panda IgG1 hinge region substantially improves structural stability, reducing degradation fragments, increasing monomer purity, and unexpectedly enhancing antigen-binding affinity by over 30-fold. This study provides a structure-guided Fc engineering strategy for developing chimeric antibodies in giant pandas, offering a promising candidate for CDV protection and a generalizable framework for conservation medicine.

AntibodiesVol. 15(6)
Chengdu Research Base of Giant Panda Breeding (CN), Sichuan Agricultural University (CN), Chongqing Academy of Animal Science (CN), Northeast Forestry University (CN)
Openalex Percentile: Top 14%
Monoclonal and Polyclonal Antibodies Research
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