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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:空间异构蛋白-水-糖结构

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摘要

We report investigations on the properties of nanoenvironments around single-GFP-mut2 proteins in trehalose-water matrixes. Single-GFPmut2 molecules embedded in thin trehalose-water films were characterized in terms of their fluorescence brightness, bleaching dynamics, excited state lifetime, and fluorescence polarization. For each property, sets of ∼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 fluorescence 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 fluids and in nonsolid carbohydrate glasses and gives a pictorial representation of the sharp, sudden reorganization of the above structures after uptake ⇆ 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。嵌入在海藻糖薄膜中的单GFPmut2分子的荧光亮度,漂白动力学,激发态寿命和荧光偏振特性得到了表征。对于每种性质,已研究了海藻糖含量和水合度的约100–150个单分子集。已经发现了三个不同的,相互转换的蛋白质家族,它们在漂白动力学,亮度和荧光偏振方面差异很大,它们的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流体和非固体碳水化合物玻璃中众所周知的异质动力学一致,并给出了吸收水分子释放后上述结构急剧,突然重组的图示。

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