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Carbohydrate dynamics at a micellar surface: GD1a headgroup transformations revealed by NMR spectroscopy.

机译:胶束表面的碳水化合物动力学:NMR光谱显示GD1a头基转变。

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摘要

The conformational dynamics of the carbohydrate headgroup of ganglioside GD1a, NeuAc alpha 2-->3Gal beta 1-->3GalNAc beta 1-->4[NeuAc alpha 2-->3]Gal beta 1-->4Glc beta 1-->1Cer, anchored in a perdeuterated dodecylphosphocholine micelle in aqueous solution, were probed by high resolution NMR spectroscopy. The observed 1H/1H NOE interactions revealed conformational averaging of the terminal NeuAc alpha 2-->3Gal and Gal beta 1-->3GalNAc glycosidic linkages. The pronounced flexibility of this trisaccharide moiety was substantiated further by two-dimensional proton-detected 13C T1, T1 rho and 1H/13C NOE measurements. The anchoring effect of the micelle allowed the detection of conformational fluctuations of the headgroup on the time scale of a few hundred picoseconds. NMR experiments performed on the GD1a/DPC micelles in H2O at low temperatures permitted the observation of hydroxyl proton resonances, contributing valuable conformational information.
机译:神经节苷脂GD1a,NeuAc alpha 2-> 3Gal beta 1-> 3GalNAc beta 1-> 4 [NeuAc alpha 2-> 3] Gal beta 1-> 4Glc beta 1--的碳水化合物头基的构象动力学通过高分辨率NMR光谱探测锚定在水溶液中的氘化十二烷基磷酸胆碱胶束中的> 1Cer。观察到的1H / 1H NOE相互作用揭示了末端NeuAc alpha 2-> 3Gal和Gal beta 1-> 3GalNAc糖苷键的构象平均。通过二维质子检测的13C T1,T1 rho和1H / 13C NOE测量进一步证实了该三糖部分的显着柔性。胶束的锚定作用允许在几百皮秒的时间尺度上检测头基的构象波动。在低温下对H2O中GD1a / DPC胶束进行的NMR实验允许观察到羟基质子共振,从而提供了有价值的构象信息。

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