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7UJJ

Stx2a and DARPin complex

7UJJ の概要
エントリーDOI10.2210/pdb7ujj/pdb
EMDBエントリー26563
分子名称DARPin, Shiga-like toxin 2 subunit A, Shiga-like toxin 2 subunit B, ... (8 entities in total)
機能のキーワードdarpin, shiga toxin, antitoxin
由来する生物種Synthetic construct
詳細
タンパク質・核酸の鎖数7
化学式量合計94135.21
構造登録者
Jiang, M.,Zhang, J. (登録日: 2022-03-30, 公開日: 2023-04-12, 最終更新日: 2024-11-13)
主引用文献Zeng, Y.,Jiang, M.,Robinson, S.,Peng, Z.,Chonira, V.,Simeon, R.,Tzipori, S.,Zhang, J.,Chen, Z.
A Multi-Specific DARPin Potently Neutralizes Shiga Toxin 2 via Simultaneous Modulation of Both Toxin Subunits.
Bioengineering (Basel), 9:-, 2022
Cited by
PubMed Abstract: Shiga toxin-producing (STEC) is a common cause of bloody diarrhea. The pathology of STEC infection derives from two exotoxins-Shiga toxin 1 (Stx1) and Shiga toxin 2 (Stx2)-that are secreted by STEC in the gut, from where they are systemically absorbed, causing severe kidney damage leading to hemolytic uremic syndrome (HUS). Currently, there is no effective treatment for HUS, and only supportive care is recommended. We report the engineering of a panel of designed ankyrin repeat proteins (DARPin) with potent neutralization activity against Stx2a, the major subtype associated with HUS. The best dimeric DARPin, SD5, created via a combination of directed evolution and rational design, neutralizes Stx2a with a half maximal effective concentration (EC) of 0.61 nM The two monomeric DARPin constituents of SD5 exhibit complementary functions-SHT targets the enzymatic A subunit of Stx2a and inhibits the toxin's catalytic activity, while DARPin #3 binds the B subunit, based on the cryo-EM study, and induces a novel conformational change in the B subunit that distorts its five-fold symmetry and presumably interferes with toxin attachment to target cells. SD5 was fused to an albumin-binding DARPin, and the resulting trimeric DARPin DA1-SD5 efficiently protects mice in a toxin challenge model, pointing to a high potential of this DARPin as a therapeutic for STEC infection. Finally, the unprecedented toxin conformational change induced by DARPin #3 represents a novel mode of action for neutralizing Stx2 toxicity and reveals new targets for future drug development.
PubMed: 36290479
DOI: 10.3390/bioengineering9100511
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (6.5 Å)
構造検証レポート
Validation report summary of 7ujj
検証レポート(詳細版)ダウンロードをダウンロード

227561

件を2024-11-20に公開中

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