首页> 美国卫生研究院文献>Proceedings of the National Academy of Sciences of the United States of America >NMR spectroscopy in studies of light-induced structural changesin mammalian rhodopsin: Applicability of solution 19F NMR
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NMR spectroscopy in studies of light-induced structural changesin mammalian rhodopsin: Applicability of solution 19F NMR

机译:NMR光谱研究光致结构变化视紫红质中的应用:19F NMR溶液的适用性

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摘要

We report high resolution solution 19F NMR spectra of fluorine-labeled rhodopsin mutants in detergent micelles. Single cysteine substitution mutants in the cytoplasmic face of rhodopsin were labeled by attachment of the trifluoroethylthio (TET), CF3-CH2-S, group through a disulfide linkage. TET-labeled cysteine mutants at amino acid positions 67, 140, 245, 248, 311, and 316 in rhodopsin were thus prepared. Purified mutant rhodopsins (6–10 mg), in dodecylmaltoside, were analyzed at 20°C by solution 19F NMR spectroscopy. The spectra recorded in the dark showed the following chemical shifts relative to trifluoroacetate: Cys-67, 9.8 ppm; Cys-140, 10.6 ppm; Cys-245, 9.9 ppm; Cys-248, 9.5 ppm; Cys-311, 9.9 ppm; and Cys-316, 10.0 ppm. Thus, all mutants showed chemical shifts downfield that of free TET (6.5 ppm). On illumination to form metarhodopsin II, upfield changes in chemical shift were observed for 19F labels at positions 67 (−0.2 ppm) and 140 (−0.4 ppm) and downfield changes for positions 248 (+0.1 ppm) and 316 (+0.1 ppm) whereas little or no change wasobserved at positions 311 and 245. On decay of metarhodopsin II, thechemical shifts reverted largely to those originally observed in thedark. The results demonstrate the applicability of solution19F NMR spectroscopy to studies of the tertiarystructures in the cytoplasmic face of intact rhodopsin in the dark andon light activation.
机译:我们报告了清洁剂胶束中氟标记的视紫红质突变体的高分辨率溶液 19 NMR光谱。视紫红质细胞质表面的单个半胱氨酸取代突变体通过二硫键连接三氟乙硫基(TET)CF3-CH2-S基团进行标记。由此制备了视紫红质中位于氨基酸位置67、140、245、248、311和316的TET标记的半胱氨酸突变体。在十二烷基麦芽糖苷中纯化的突变型视紫红质(6-10 mg)在20°C下通过溶液 19 F NMR光谱分析。在黑暗中记录的光谱相对于三氟乙酸盐显示出以下化学位移:Cys-67,9.8ppm; Cys-67,9.8ppm。 Cys-140,10.6 ppm; Cys-245,9.9 ppm; Cys-248,9.5 ppm;半胱氨酸311,9.9 ppm; Cys-316为10.0 ppm。因此,所有突变体均显示出游离TET(6.5 ppm)的低化学位移。照亮形成视紫红质II时,在位置67(-0.2 ppm)和140(-0.4 ppm)的 19 F标签上观察到化学位移的高场变化,在位置248(+0.1 ppm)处观察到低场变化)和316(+0.1 ppm),而变化很小或没有变化在第311和245位观察到。化学位移在很大程度上恢复为最初在暗。结果证明了该解决方案的适用性 19 F NMR光谱法研究第三级在黑暗和黑暗中完整视紫红质细胞质表面的结构在光激活。

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