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Quantitative Imaging of Molecular Order in Lipid Membranes Using Two-Photon Fluorescence Polarimetry

机译:使用双光子荧光偏振光定量成像的脂质膜中的分子顺序。

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摘要

We present a polarimetric two-photon microscopy technique to quantitatively image the local static molecular orientational behavior in lipid and cell membranes. This approach, based on a tunable excitation polarization state complemented by a polarized readout, is easily implementable and does not require hypotheses on the molecular angular distribution such as its mean orientation, which is a main limitation in traditional fluorescence anisotropy measurements. The method is applied to the investigation of the molecular angular distribution in giant unilamellar vesicles formed by liquid-ordered and liquid-disordered micro-domains, and in COS-7 cell membranes. The highest order contrast between ordered and disordered domains is obtained for dyes locating within the membrane acyl chains.
机译:我们提出了一种偏振两光子显微镜技术,以定量成像脂质和细胞膜中的局部静态分子取向行为。这种方法基于可调谐的激发偏振态,并通过极化读数进行补充,易于实现,并且不需要分子角分布(例如其平均方向)的假设,这是传统荧光各向异性测量的主要限制。该方法用于研究由液体有序和液体无序的微区形成的巨大单层囊泡以及COS-7细胞膜的分子角分布。对于位于膜酰基链内的染料,可以获得有序域和无序域之间的最高阶对比度。

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