Size-dependent effect of site-specific polyethylene glycol modification of trastuzumab on the antibody functions
Abstract
Polymer modification of antibodies has attracted attention for enhancing antibody functionality. Modification with polyethylene glycol (PEG) or biopolymers such as antibody-oligonucleotide conjugates has been investigated. Although direct effects at the modification site have been understood, distal effects of modifications on intrinsic antibody functions such as antigen-binding and Fc receptor-binding activities remain poorly characterized. In this study, we prepared site-specifically PEGylated trastuzumab to evaluate the effects of the modification site and the size of PEG chains on antibody functions. Reporter gene assays revealed a significant reduction in antibody-dependent cell cytotoxicity (ADCC) activity in a site- and size-dependent manner. Both the reduction in interaction with the antigen and Fc{gamma}RIIIa were observed in a size-dependent manner. Interestingly, the effect of the modification site was only observed for ADCC activity, which suggests that the higher-order structure of the modified antibody plays a critical role in effector function. These results provide molecular design guidelines for the polymer modification of antibodies.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Proximity directs microbial transglutaminase site selectivity in native antibody modification
Riko Nishioka, Koki Murozono, … Noriho Kamiya·bioRxiv·Aug 20, 2026
- The structural basis for distinct binding avidity of Pertuzumab and Trastuzumab IgM towards HER2
F. Samsudin, J. Y. Yeo, … P. Bond·bioRxiv·Jul 21, 2019
- The increased hinge flexibility of an IgG1-IgG3 hybrid monoclonal enhances Fc-mediated protection against group A streptococci
Arman Izadi, Yasaman Karami, … Pontus Nordenfelt·bioRxiv·Oct 14, 2023
- An Unexpected Single-step Glycosylation Enables the Construction of Antibody-Biomacromolecule Conjugates as Therapeutics
Y. Yang, Z. t. Song, … J. P. Li·bioRxiv·Sep 4, 2022
- An atomistic perspective on ADCC quenching by core-fucosylation of IgG1 Fc N-glycans from enhanced sampling molecular dynamics
A. M. Harbison, E. Fadda·bioRxiv·Jul 15, 2019
- Engineering affinity-matured variants of an anti-polysialic acid monoclonal antibody with superior cytotoxicity-mediating potency
Wei‐Yao Wang, Mehman I. Bunyatov, … Matthew P. DeLisa·Cell chemical biologyPeer-reviewed·Jan 1, 2025