Abstract
Engineering of Fc for improved affinity to its receptor, FcγRIIIa, can enhance the therapeutic activity of monoclonal antibodies. S239D/I332E mutation of Fc has been extensively employed in various Fc engineering studies. Still, it is not clear how the mutations have structurally influenced the molecular interactions between Fc and FcγRIIIa. In this study, the point or combined mutations of S239D/I332E were introduced into one chain (A) or the other chain (chain B) of the homodimeric Fc domain computationally. Their structural effects on the binding to FcγRIIIa were investigated through a computational docking method. These results showed that the chain-specific point mutation, S239D induced a new salt-bridge with the receptor in A and B chains of Fc, whereas I332E mutation generated a new salt-bridge with the receptor only in A chain. The combined mutation study identified that the Fc variant with four mutations reproduced the three salt-bridges. This showed that the mutation of S239D and I332E in chain A of Fc induced complex salt-bridge formation with the Lys158 of FcγRIIIa. This study is expected to provide more structural insight into Fc variants’ design based on S239D/I332E mutation.
Original language | English |
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Pages (from-to) | 985-992 |
Number of pages | 8 |
Journal | Biotechnology and Bioprocess Engineering |
Volume | 26 |
Issue number | 6 |
DOIs | |
Publication status | Published - 2021 Dec |
Bibliographical note
Funding Information:This research was supported by Basic Science Research Program through the National Research Foundation of Korea(NRF) funded by the Ministry of Education (2021R1I1A3050836).
Publisher Copyright:
© 2021, The Korean Society for Biotechnology and Bioengineering and Springer.
Keywords
- Fc
- FcγRIIIa
- in silico mutation
- protein-protein docking
- salt-bridges
ASJC Scopus subject areas
- Biotechnology
- Bioengineering
- Applied Microbiology and Biotechnology
- Biomedical Engineering