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3T2N

Human hepsin protease in complex with the Fab fragment of an inhibitory antibody

3T2N の概要
エントリーDOI10.2210/pdb3t2n/pdb
関連するPDBエントリー1O5E 1P57 1Z8G
分子名称Serine protease hepsin, Antibody, Fab fragment, Heavy Chain, Antibody, Fab fragment, Light Chain, ... (4 entities in total)
機能のキーワードtype ii transmembrane serine protease, srcr domain, substrates include pro-hepsin, pro-hgf, laminin-332, transmembrane, hydrolase
由来する生物種Homo sapiens (human)
詳細
細胞内の位置Membrane; Single-pass type II membrane protein: P05981
タンパク質・核酸の鎖数6
化学式量合計174682.21
構造登録者
主引用文献Koschubs, T.,Dengl, S.,Durr, H.,Kaluza, K.,Georges, G.,Hartl, C.,Jennewein, S.,Lanzendorfer, M.,Auer, J.,Stern, A.,Huang, K.S.,Packman, K.,Gubler, U.,Kostrewa, D.,Ries, S.,Hansen, S.,Kohnert, U.,Cramer, P.,Mundigl, O.
Allosteric antibody inhibition of human hepsin protease.
Biochem.J., 442:483-494, 2012
Cited by
PubMed Abstract: Hepsin is a type II transmembrane serine protease that is expressed in several human tissues. Overexpression of hepsin has been found to correlate with tumour progression and metastasis, which is so far best studied for prostate cancer, where more than 90% of such tumours show this characteristic. To enable improved future patient treatment, we have developed a monoclonal humanized antibody that selectively inhibits human hepsin and does not inhibit other related proteases. We found that our antibody, hH35, potently inhibits hepsin enzymatic activity at nanomolar concentrations. Kinetic characterization revealed non-linear, slow, tight-binding inhibition. This correlates with the crystal structure we obtained for the human hepsin-hH35 antibody Fab fragment complex, which showed that the antibody binds hepsin around α3-helix, located far from the active centre. The unique allosteric mode of inhibition of hH35 is distinct from the recently described HGFA (hepatocyte growth factor activator) allosteric antibody inhibition. We further explain how a small change in the antibody design induces dramatic structural rearrangements in the hepsin antigen upon binding, leading to complete enzyme inactivation.
PubMed: 22132769
DOI: 10.1042/BJ20111317
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.55 Å)
構造検証レポート
Validation report summary of 3t2n
検証レポート(詳細版)ダウンロードをダウンロード

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件を2026-02-11に公開中

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