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GFP-mut2 proteins in trehalose-water matrixes: Spatially heterogeneous protein-water-sugar structures

机译:海藻糖-水基质中的GFP-mut2蛋白:空间异质性蛋白-水-糖结构

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摘要

We report investigations on the properties of nanoenvironments around single-GFP-mut2 proteins in trehalosewater matrixes. Single-GFPmut2 molecules embedded in thin trehalose-water. lms were characterized in terms of their. uorescence brightness, bleaching dynamics, excited state lifetime, and. uorescence polarization. For each property, sets of similar to 100-150 single molecules have been investigated as a function of trehalose content and hydration. Three distinct and interconverting families of proteins have been found which differ widely in terms of bleaching dynamics, brightness, and. uorescence polarization, whose relative populations sizably depend on sample hydration. The reported results evidence the simultaneous presence of different protein-trehalose-water nanostructures whose rigidity increases by lowering the sample hydration. Such spatial inhomogeneity is in line with the well-known heterogeneous dynamics in supercooled. uids and in nonsolid carbohydrate glasses and gives a pictorial representation of the sharp, sudden reorganization of the above structures after uptake reversible arrow release of water molecules.
机译:我们报告有关海藻糖水基质中的单个GFP-mut2蛋白周围的纳米环境的性质的调查。单GFPmut2分子嵌入在海藻糖稀水中。 lms的特征在于它们。荧光亮度,漂白动力学,激发态寿命以及荧光偏振。对于每种性质,已经研究了海藻糖含量和水合作用的类似于100-150个单分子的集合。已经发现了三个不同的和相互转换的蛋白质家族,它们在漂白动力学,亮度和方面差异很大。荧光偏振,其相对种群很大程度上取决于样品的水合作用。报告的结果证明同时存在着不同的蛋白质-海藻糖-水纳米结构,这些结构通过降低样品的水合作用而提高了刚性。这种空间不均匀性与过冷中众所周知的异质动力学相符。液体和非固体碳水化合物玻璃中,并给出了摄取可逆箭头释放水分子后上述结构急剧,突然重组的图示。

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