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2022 Fiscal Year Final Research Report

Understanding the efficacy of therapeutic antibodies through their interaction with cellular receptors.

Research Project

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Project/Area Number 20H03228
Research Category

Grant-in-Aid for Scientific Research (B)

Allocation TypeSingle-year Grants
Section一般
Review Section Basic Section 43040:Biophysics-related
Research InstitutionKyushu University

Principal Investigator

CAAVEIRO Jose  九州大学, 薬学研究院, 教授 (00536732)

Co-Investigator(Kenkyū-buntansha) 高橋 大輔  九州大学, 薬学研究院, 講師 (70791523)
Project Period (FY) 2020-04-01 – 2023-03-31
KeywordsAntibody / Fc receptor / hinge / structure / immunology / glycosylation / bnAbs / HIV-1
Outline of Final Research Achievements

We advanced the understanding of the interaction between antibodies of the IgG family and their cellular receptors at the molecular level. We have described the less-than expected effect of mutations in the middle hinge region to the strength of the interaction with receptors (the middle hinge is where the disulfide bond is located). However, residues in close proximity to the binding interface had a profound effect. Our studies support the engineering of antibodies in the hinge region without major effect in the potency of Abs.
Additionally, we made an important contribution to improve the potency of Abs. This process was patented and consist on (i) the introduction of a CYS residue in a strategic location and (2) chemical modification of the CYS residue by a yodo acetamide molecule of specific atomic structure. Using this approach we have improved the potency of anti-HIV-1 Abs by more than 500-fold.

Free Research Field

43040 Biophysics related

Academic Significance and Societal Importance of the Research Achievements

From a scientific point, we have advanced the basic knowledge of the interaction between antibodies and their cellular receptors. From a social point of view, the technology discovered herein improves the potency of antibodies and might save the lives of people suffering from infectious diseases.

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Published: 2024-01-30  

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