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首页> 外文期刊>Protein engineering design & selection: PEDS >A set of multicolored Photinus pyralis luciferase mutants for in vivo bioluminescence applications
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A set of multicolored Photinus pyralis luciferase mutants for in vivo bioluminescence applications

机译:一组用于体内生物发光应用的彩色Photinus pyralis荧光素酶突变体

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Error-prone PCR was used to isolate Photinus pyralis luciferase mutants producing bright light in the red-orange region of the spectrum. All mutations were clustered in the beta 5-alpha 10-beta 6 region of N-terminal subdomain B and appear to affect bioluminescence color by modulating the position of the Ser(314)-Leu(319) mobile loop with respect to the putative active site. Two red variants (Q283R and S284G) and one orange mutant (S293P) contained a single substitution. Although the remaining orange variant contained two mutations, L287I mainly contributed to the color change. Emission spectra collected on whole cells at pH 7.0 revealed that while a single peak of lambda(max) approximate to 605 nm accounts for red light production by the Q283R and S284G variants, orange light results from the contribution of two peaks of lambda(max) approximate to 560 and 600 nm. All spectra underwent a red-shift when cells were assayed under acidic conditions, whereas a blue-shift was observed at pH 8.0, indicating that the internal pH of Escherichia coli is close to the external pH shortly after imposition of acid or alkaline stress. In addition, changes in assay pH led to bimodal emission spectra, lending support to the idea that bioluminescence color is determined by the relative contribution of yellow-green and red-orange peaks. The set of multicolored luciferase mutants described here may prove useful for a variety of applications including biosensing, pH monitoring, and tissue and animal imaging.
机译:容易出错的PCR被用于分离在光谱的橘红色区域中产生亮光的Photinus pyralis萤光素酶突变体。所有突变都聚集在N末端亚结构域B的beta 5-alpha 10-beta 6区域,并且似乎通过调节Ser(314)-Leu(319)移动环相对于假定的活性分子的位置来影响生物发光颜色现场。两个红色变体(Q283R和S284G)和一个橙色突变体(S293P)包含一个取代基。尽管剩余的橙色变体包含两个突变,但L287I主要促成颜色变化。在pH 7.0的全细胞上收集的发射光谱表明,虽然Q283R和S284G变体产生的红色光产生了大约605 nm的lambda(max)单个峰,但橙色光却来自两个lambda(max)峰的贡献。大约为560和600 nm。在酸性条件下测定细胞时,所有光谱均发生红移,而在pH 8.0处观察到蓝移,表明在施加酸或碱胁迫后不久,大肠杆菌的内部pH接近外部pH。此外,测定pH的变化导致了双峰发射光谱,这为生物发光颜色由黄绿色和红色橙色峰的相对贡献所决定的观点提供了支持。此处描述的多色萤光素酶突变体集可证明可用于多种应用,包括生物传感,pH监测以及组织和动物成像。

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