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-Structure paper
| タイトル | Conversion of an agonistic anti-TNFR2 biparatopic antibody into an antagonist by insertion of peptide linkers into the hinge region. |
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| ジャーナル・号・ページ | J Biol Chem, Vol. 301, Issue 9, Page 110548, Year 2025 |
| 掲載日 | 2025年7月31日 |
著者 | Takuya Otsuki / Shigeyuki Matsumoto / Junso Fujita / Tomoko Miyata / Keiichi Namba / Ryo Kanada / Yasushi Okuno / Haruhiko Kamada / Hiroaki Ohno / Hiroki Akiba / ![]() |
| PubMed 要旨 | Biparatopic antibodies (BpAbs) bind two different antigen epitopes to form characteristic immunocomplexes. Many BpAbs have been developed for enhanced crosslinking to induce signal transduction or ...Biparatopic antibodies (BpAbs) bind two different antigen epitopes to form characteristic immunocomplexes. Many BpAbs have been developed for enhanced crosslinking to induce signal transduction or cell internalization, whereas few have been reported with smaller immunocomplexes to suppress unwanted signaling. Here, we developed a strategy to induce 1:1 immunocomplex formation to maximize antagonistic function. Various peptide linkers were introduced into the hinge regions of IgG-like agonist BpAbs against tumor necrosis factor receptor 2. Loss of crosslinking activity was observed for one BpAb, allowing the conversion of its function from an agonist to an antagonist. However, crosslinking activity was retained for another agonist, BpAb, which binds to a different epitope pair. In a combined analysis of cryo-electron microscopy and coarse-grained molecular dynamics simulations, the effect of epitope combination on the stability of 1:1 complexes was observed. These results lead to an understanding of the mechanism and design of BpAbs to adopt a 1:1-binding mode. |
リンク | J Biol Chem / PubMed:40752574 / PubMed Central |
| 手法 | EM (単粒子) |
| 解像度 | 3.73 Å |
| 構造データ | EMDB-63050, PDB-9lfl: |
| 由来 |
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キーワード | IMMUNE SYSTEM / Antibody / biparatopic antibody / antagonist |
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