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2QYJ

Crystal structure of a designed full consensus ankyrin

2QYJ の概要
エントリーDOI10.2210/pdb2qyj/pdb
分子名称ankyrin NI3C, SULFATE ION (3 entities in total)
機能のキーワードankyrin repeat, repeat protein, helix-turn-helix-beta-turn, de novo protein
タンパク質・核酸の鎖数1
化学式量合計18310.35
構造登録者
Merz, T. (登録日: 2007-08-15, 公開日: 2007-11-13, 最終更新日: 2023-10-25)
主引用文献Merz, T.,Wetzel, S.K.,Firbank, S.,Pluckthun, A.,Grutter, M.G.,Mittl, P.R.E.
Stabilizing ionic interactions in a full-consensus ankyrin repeat protein.
J.Mol.Biol., 376:232-240, 2008
Cited by
PubMed Abstract: Full-consensus designed ankyrin repeat proteins (DARPins), in which randomized positions of the previously described DARPin library have been fixed, are characterized. They show exceptionally high thermodynamic stabilities, even when compared to members of consensus DARPin libraries and even more so when compared to naturally occurring ankyrin repeat proteins. We determined the crystal structure of a full-consensus DARPin, containing an N-capping repeat, three identical internal repeats and a C-capping repeat at 2.05 A resolution, and compared its structure with that of the related DARPin library members E3_5 and E3_19. This structural comparison suggests that primarily salt bridges on the surface, which arrange in a network with almost crystal-like regularity, increase thermostability in the full-consensus NI(3)C DARPin to make it resistant to boiling. In the crystal structure, three sulfate ions complement this network. Thermal denaturation experiments in guanidine hydrochloride directly indicate a contribution of sulfate binding to the stability, providing further evidence for the stabilizing effect of surface-exposed electrostatic interactions and regular charge networks. The charged residues at the place of randomized residues in the DARPin libraries were selected based on sequence statistics and suggested that the charge interaction network is a hidden design feature of this protein family. Ankyrins can therefore use design principles from proteins of thermophilic organisms and reach at least similar stabilities.
PubMed: 18155045
DOI: 10.1016/j.jmb.2007.11.047
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (2.05 Å)
構造検証レポート
Validation report summary of 2qyj
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2024-11-06に公開中

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