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Quantitative sensing of microviscosity in protocells and amyloid materials using fluorescence lifetime imaging of molecular rotors

机译:使用分子转子的荧光寿命成像定量检测原细胞和淀粉样物质中的微粘度

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Molecular rotors are fluorophores that have a fluorescence quantum yield that depends upon intermolecular rotation. The fluorescence quantum yield, intensity and lifetime of molecular rotors all vary as functions of viscosity, as high viscosities inhibit intermolecular rotation and cause an increase in the non-radiative decay rate. As such, molecular rotors can be used to probe viscosity on microscopic scales. Here, we apply fluorescence lifetime imaging microscopy (FLIM) to measure the fluorescence lifetimes of three different molecular rotors, in order to determine the microscopic viscosity in two model systems with significant biological interest. First, the constituents of a novel protocell - a model of a prebiotic cell - were studied using the molecular rotors BODIPY C_(10) and kiton red. Second, amyloid formation was investigated using the molecular rotor Cy3.
机译:分子转子是具有取决于分子间旋转的荧光量子产率的荧光团。分子转子的荧光量子产率,强度和寿命都随粘度而变化,因为高粘度会抑制分子间旋转并导致非辐射衰变速率增加。这样,分子转子可用于在微观尺度上探测粘度。在这里,我们应用荧光寿命成像显微镜(FLIM)来测量三个不同分子转子的荧光寿命,以便确定具有重大生物学意义的两个模型系统的微观粘度。首先,使用分子转子BODIPY C_(10)和Kiton red研究了新型原生细胞(益生元细胞模型)的成分。其次,使用分子转子Cy3研究淀粉样蛋白的形成。

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