6VCA

TB38 complex

6VCA の概要

• エントリーDOI: 10.2210/pdb6vca/pdb
• 関連するPDBエントリー: 6vc9
• 分子名称: 5'-nucleotidase, ecto (CD73), isoform CRA_a, TB38 heavy chain, TB38 light chain, ... (6 entities in total)
• 機能のキーワード: fab, enzyme, immune system
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 12
• 化学式量合計: 428805.50

構造登録者

Zhou, Y.F.,Lord, D.M. (登録日: 2019-12-20, 公開日: 2020-11-11, 最終更新日: 2024-10-30)

主引用文献

Stefano, J.E.,Lord, D.M.,Zhou, Y.,Jaworski, J.,Hopke, J.,Travaline, T.,Zhang, N.,Wong, K.,Lennon, A.,He, T.,Bric-Furlong, E.,Cherrie, C.,Magnay, T.,Remy, E.,Brondyk, W.,Qiu, H.,Radosevic, K.
A highly potent CD73 biparatopic antibody blocks organization of the enzyme active site through dual mechanisms.
J.Biol.Chem., 295:18379-18389, 2020

PubMed Abstract: The dimeric ectonucleotidase CD73 catalyzes the hydrolysis of AMP at the cell surface to form adenosine, a potent suppressor of the immune response. Blocking CD73 activity in the tumor microenvironment can have a beneficial effect on tumor eradication and is a promising approach for cancer therapy. Biparatopic antibodies binding different regions of CD73 may be a means to antagonize its enzymatic activity. A panel of biparatopic antibodies representing the pairwise combination of 11 parental monoclonal antibodies against CD73 was generated by Fab-arm exchange. Nine variants vastly exceeded the potency of their parental antibodies with ≥90% inhibition of activity and subnanomolar EC values. Pairing the Fabs of parents with nonoverlapping epitopes was both sufficient and necessary whereas monovalent antibodies were poor inhibitors. Some parental antibodies yielded potent biparatopics with multiple partners, one of which (TB19) producing the most potent. The structure of the TB19 Fab with CD73 reveals that it blocks alignment of the N- and C-terminal CD73 domains necessary for catalysis. A separate structure of CD73 with a Fab (TB38) which complements TB19 in a particularly potent biparatopic shows its binding to a nonoverlapping site on the CD73 N-terminal domain. Structural modeling demonstrates a TB19/TB38 biparatopic antibody would be unable to bind the CD73 dimer in a bivalent manner, implicating crosslinking of separate CD73 dimers in its mechanism of action. This ability of a biparatopic antibody to both crosslink CD73 dimers and fix them in an inactive conformation thus represents a highly effective mechanism for the inhibition of CD73 activity.

PubMed: 33122192
DOI: 10.1074/jbc.RA120.012395

実験手法

X-RAY DIFFRACTION (3.73 Å)