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8AUR

Cryo-EM structure of a TasA fibre

8AUR の概要
エントリーDOI10.2210/pdb8aur/pdb
EMDBエントリー15673
分子名称Major biofilm matrix component (1 entity in total)
機能のキーワードbiofilm matrix fibre, protein fibril
由来する生物種Bacillus subtilis
タンパク質・核酸の鎖数3
化学式量合計77302.96
構造登録者
Boehning, J.,Bharat, T.A.M. (登録日: 2022-08-25, 公開日: 2022-11-30, 最終更新日: 2025-07-09)
主引用文献Bohning, J.,Ghrayeb, M.,Pedebos, C.,Abbas, D.K.,Khalid, S.,Chai, L.,Bharat, T.A.M.
Donor-strand exchange drives assembly of the TasA scaffold in Bacillus subtilis biofilms.
Nat Commun, 13:7082-7082, 2022
Cited by
PubMed Abstract: Many bacteria in nature exist in multicellular communities termed biofilms, where cells are embedded in an extracellular matrix that provides rigidity to the biofilm and protects cells from chemical and mechanical stresses. In the Gram-positive model bacterium Bacillus subtilis, TasA is the major protein component of the biofilm matrix, where it has been reported to form functional amyloid fibres contributing to biofilm structure and stability. Here, we present electron cryomicroscopy structures of TasA fibres, which show that, rather than forming amyloid fibrils, TasA monomers assemble into fibres through donor-strand exchange, with each subunit donating a β-strand to complete the fold of the next subunit along the fibre. Combining electron cryotomography, atomic force microscopy, and mutational studies, we show how TasA fibres congregate in three dimensions to form abundant fibre bundles that are essential for B. subtilis biofilm formation. Our study explains the previously observed biochemical properties of TasA and shows how a bacterial extracellular globular protein can assemble from monomers into β-sheet-rich fibres, and how such fibres assemble into bundles in biofilms.
PubMed: 36400765
DOI: 10.1038/s41467-022-34700-z
主引用文献が同じPDBエントリー
実験手法
ELECTRON MICROSCOPY (3.47 Å)
構造検証レポート
Validation report summary of 8aur
検証レポート(詳細版)ダウンロードをダウンロード

250059

件を2026-03-04に公開中

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