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2H3H

Crystal structure of the liganded form of Thermotoga maritima glucose binding protein

2H3H の概要
エントリーDOI10.2210/pdb2h3h/pdb
分子名称Sugar ABC transporter, periplasmic sugar-binding protein, beta-D-glucopyranose (3 entities in total)
機能のキーワードglucose binding protein, periplasmic binding protein, gbp, sugar binding protein
由来する生物種Thermotoga maritima
タンパク質・核酸の鎖数2
化学式量合計68166.32
構造登録者
Changela, A.,Tian, Y. (登録日: 2006-05-22, 公開日: 2007-05-22, 最終更新日: 2023-08-30)
主引用文献Tian, Y.,Cuneo, M.J.,Changela, A.,Hocker, B.,Beese, L.S.,Hellinga, H.W.
Structure-based design of robust glucose biosensors using a Thermotoga maritima periplasmic glucose-binding protein.
Protein Sci., 16:2240-2250, 2007
Cited by
PubMed Abstract: We report the design and engineering of a robust, reagentless fluorescent glucose biosensor based on the periplasmic glucose-binding protein obtained from Thermotoga maritima (tmGBP). The gene for this protein was cloned from genomic DNA and overexpressed in Escherichia coli, the identity of its cognate sugar was confirmed, ligand binding was studied, and the structure of its glucose complex was solved to 1.7 Angstrom resolution by X-ray crystallography. TmGBP is specific for glucose and exhibits high thermostability (midpoint of thermal denaturation is 119 +/- 1 degrees C and 144 +/- 2 degrees C in the absence and presence of 1 mM glucose, respectively). A series of fluorescent conjugates was constructed by coupling single, environmentally sensitive fluorophores to unique cysteines introduced by site-specific mutagenesis at positions predicted to be responsive to ligand-induced conformational changes based on the structure. These conjugates were screened to identify engineered tmGBPs that function as reagentless fluorescent glucose biosensors. The Y13C*Cy5 conjugate is bright, gives a large response to glucose over concentration ranges appropriate for in vivo monitoring of blood glucose levels (1-30 mM), and can be immobilized in an orientation-specific manner in microtiter plates to give a reversible response to glucose. The immobilized protein retains its response after long-term storage at room temperature.
PubMed: 17766373
DOI: 10.1110/ps.072969407
主引用文献が同じPDBエントリー
実験手法
X-RAY DIFFRACTION (1.7 Å)
構造検証レポート
Validation report summary of 2h3h
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2026-04-15に公開中

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