首页> 外文会议>12th Symposium on Bioluminescence and Chemiluminescence, Apr 5-9, 2002, Robinson College, University of Cambridge, UK >PHOTOTRANSFORMATION OF THE WILD-TYPE AEQUOREA VICTORIA GREEN FLUORESCENT PROTEIN WITH UV- AND VISIBLE LIGHT LEADS TO DECARBOXYLATION OF GLUTAMATE 222
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PHOTOTRANSFORMATION OF THE WILD-TYPE AEQUOREA VICTORIA GREEN FLUORESCENT PROTEIN WITH UV- AND VISIBLE LIGHT LEADS TO DECARBOXYLATION OF GLUTAMATE 222

机译:带有紫外和可见光铅的野生型紫杉维多利亚绿色荧光蛋白的光转化以使谷氨酸222脱羧

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Phototransformation of Aequorea victoria Green Fluorescent Protein (GFP) was discovered shortly after the cloning of the gfp gene. UV/Vis light transforms the species absorbing at 398 nm (GFP_(398)), with a neutral, phenolic chromophore, into an ionic species absorbing at 483 nm (GFP_(483)), with a phenolate containing chromophore. Besides its role as transient proton acceptor in the excited state, Glu 222 has also been suggested to function as the stable acceptor for the proton that is lost from the chromophore upon photoconversion. Conformational changes such as rotamer reorientation of a threonine side chain (Thr 203) and syn/anti-isomerisation of Glu 222 have been proposed to compete with reformation of the protonated ground state of the chromophore. However, a direct test of this model with FTIR spectroscopy turned out negative, indicating that Glu 222 is not the stable proton acceptor.
机译:克隆gfp基因后不久发现了维多利亚水母绿色荧光蛋白(GFP)的光转化。 UV / Vis光将具有中性酚生色团在398 nm(GFP_(398))处吸收的物种转换为具有含酚盐的生色团在483 nm(GFP_(483))处吸收的离子物种。除了在激发态中作为瞬态质子受体的作用外,还建议使用Glu 222作为光转化时从生色团损失的质子的稳定受体。已经提出构象变化,例如苏氨酸侧链的旋转异构体重新定向(Thr 203)和Glu 222的顺式/反异构化,以与生色团的质子化基态的重整竞争。但是,使用FTIR光谱对该模型进行的直接测试结果为阴性,表明Glu 222不是稳定的质子受体。

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