首页> 外文会议>Ultrasensitive and Single-Molecule Detection Technologies; Progress in Biomedical Optics and Imaging; vol.7 no.15 >Single molecule fluorescence spectroscopy - Approaches towards quantitative investigations of structure and dynamics in living cells
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Single molecule fluorescence spectroscopy - Approaches towards quantitative investigations of structure and dynamics in living cells

机译:单分子荧光光谱法-定量研究活细胞结构和动力学的方法

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The investigation of the structure and dynamics of biomolecules and biomolecular assemblies in living cells is of current interest in molecular biology. Recent developments in single molecule fluorescence spectroscopy (SMFS) have opened ways for investigating the dynamics and stoichiometry of individual biomolecular complexes e.g., by application of single pair fluorescence resonance energy transfer (spFRET) with alternating laser excitation (ALEX), and by improved labels and labeling techniques. In the recent years, we have developed a set of techniques that allow the determination of the spatial distribution of single fluorescent molecules and their identification by spectrally-resolved fluorescence lifetime imaging microscopy (SFLIM) as well as the observation of the dynamics of individual molecules immobilized on surfaces. Based on SFLIM we currently focus on investigating the diffusion kinetics of biomolecules in living cells. By combining high-resolution confocal fluorescence microscopy of single molecules with fluorescence correlation spectroscopy (FCS) we seek to quantitate diffusion coefficients and concentrations of relevant fluorescently labeled biomolecules within living cells thereby visualizing the heterogeneous distribution of local mobilities in the sample. The simultaneously acquired fluorescence intensity and lifetime images can further be used for additional single point measurements for obtaining i.e., information about the stoichiometry of immobilized biomolecular complexes based on photon anti-bunching. In addition the simultaneous acquisition of multiple characteristic properties by SFLIM, like spectral emission bands and fluorescence lifetime, offers the opportunity to discriminate different fluorescent probes and autofluorescence.
机译:对活细胞中生物分子和生物分子组装体的结构和动力学的研究在分子生物学中是当前感兴趣的。单分子荧光光谱法(SMFS)的最新发展为研究单个生物分子复合物的动力学和化学计量学开辟了途径,例如,通过应用单对荧光共振能量转移(spFRET)和交替激光激发(ALEX)以及改进的标记和标签技术。近年来,我们开发了一套技术,可通过光谱分辨荧光寿命成像显微镜(SFLIM)来确定单个荧光分子的空间分布并对其进行鉴定,以及观察固定化的单个分子的动力学在表面上。基于SFLIM,我们目前专注于研究生物分子在活细胞中的扩散动力学。通过将单个分子的高分辨率共聚焦荧光显微镜与荧光相关光谱法(FCS)相结合,我们寻求定量活细胞内相关荧光标记生物分子的扩散系数和浓度,从而可视化样品中局部迁移的异质分布。同时获得的荧光强度和寿命图像可以进一步用于另外的单点测量,以获得基于光子反聚束的固定化生物分子复合物的化学计量信息。此外,通过SFLIM同时获取多种特征,例如光谱发射带和荧光寿命,为区分不同的荧光探针和自发荧光提供了机会。

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