8B6R
X-ray structure of the haloalkane dehalogenase HaloTag7 labeled with a chloroalkane Cyanine3 fluorophore substrate
8B6R の概要
エントリーDOI | 10.2210/pdb8b6r/pdb |
関連するPDBエントリー | 8B6S 8B6T |
分子名称 | Haloalkane dehalogenase, ~{N}-[2-[2-(6-chloranylhexoxy)ethoxy]ethyl]-6-[3,3-dimethyl-2-[(~{E})-3-(1,3,3-trimethylindol-2-ylidene)prop-1-enyl]indol-1-ium-1-yl]hexanamide, CHLORIDE ION, ... (6 entities in total) |
機能のキーワード | haloalkane dehalogenase, halotag, halotag7, self-labeling protein, fluorophore, cyanine 3, cy3, hydrolase |
由来する生物種 | Rhodococcus sp. |
タンパク質・核酸の鎖数 | 1 |
化学式量合計 | 34317.47 |
構造登録者 | |
主引用文献 | Hellweg, L.,Edenhofer, A.,Barck, L.,Huppertz, M.C.,Frei, M.S.,Tarnawski, M.,Bergner, A.,Koch, B.,Johnsson, K.,Hiblot, J. A general method for the development of multicolor biosensors with large dynamic ranges. Nat.Chem.Biol., 19:1147-1157, 2023 Cited by PubMed Abstract: Fluorescent biosensors enable the study of cell physiology with spatiotemporal resolution; yet, most biosensors suffer from relatively low dynamic ranges. Here, we introduce a family of designed Förster resonance energy transfer (FRET) pairs with near-quantitative FRET efficiencies based on the reversible interaction of fluorescent proteins with a fluorescently labeled HaloTag. These FRET pairs enabled the straightforward design of biosensors for calcium, ATP and NAD with unprecedented dynamic ranges. The color of each of these biosensors can be readily tuned by changing either the fluorescent protein or the synthetic fluorophore, which enables simultaneous monitoring of free NAD in different subcellular compartments following genotoxic stress. Minimal modifications of these biosensors furthermore allow their readout to be switched to fluorescence intensity, fluorescence lifetime or bioluminescence. These FRET pairs thus establish a new concept for the development of highly sensitive and tunable biosensors. PubMed: 37291200DOI: 10.1038/s41589-023-01350-1 主引用文献が同じPDBエントリー |
実験手法 | X-RAY DIFFRACTION (1.5 Å) |
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