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Single Molecule Photobleaching (SMPB) Technology for Counting of RNA DNA Protein and Other Molecules in Nanoparticles and Biological Complexes by TIRF Instrumentation

机译:单分子光漂白(SMPB)技术通过TIRF仪器对纳米颗粒和生物复合物中的RNADNA蛋白质和其他分子进行计数

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摘要

Direct counting of biomolecules within biological complexes or nanomachines is demanding. Single molecule counting using optical microscopy is challenging due to the diffraction limit. The Single Molecule Photobleaching (SMPB) technology for direct counting developed by our team (Shu et al, EMBO J, 2007, 26:527; Zhang et al, RNA, 2007, 13:1793) offers a simple and straightforward method to determine the stoichiometry of molecules or subunits within biocomplexes or nanomachines at nanometer scales. Stoichiometry is determined by real-time observation of the number of descending steps resulted from the photobleaching of individual fluorophore. This technology has now been used extensively for single molecule counting of protein, RNA, and other macromolecules in a variety of complexes or nanostructures. Here, we elucidate the SMPB technology, using the counting of RNA molecules within a bacteriophage phi29 DNA-packaging biomotor as an example. The method described here can be applied to the single molecule counting of other molecules in other systems. The construction of a concise, simple and economical single molecule total internal reflection fluorescence (TIRF) microscope combining prism-type and objective-type TIRF is described. The imaging system contains a deep-cooled sensitive EMCCD camera with single fluorophore detection sensitivity, a laser combiner for simultaneous dual-color excitation, and a Dual-View imager to split the multiple outcome signals to different detector channels based on their wavelengths. Methodology of the single molecule photobleaching assay used to elucidate the stoichiometry of RNA on phi29 DNA packaging motor and the mechanism of protein/RNA interaction are described. Different methods for single fluorophore labeling of RNA molecules are reviewed. The process of statistical modeling to reveal the true copy number of the biomolecules based on binomial distribution is also described.
机译:要求对生物复合物或纳米机器中的生物分子进行直接计数。由于衍射极限,使用光学显微镜的单分子计数是具有挑战性的。我们团队开发的用于直接计数的单分子光漂白(SMPB)技术(Shu等人,EMBO J,2007,26:527; Zhang等人,RNA,2007,13:1793)提供了一种简单而直接的方法来确定生物复合物或纳米机器中纳米级分子或亚基的化学计量。通过实时观察由单个荧光团的光漂白导致的下降步骤的数量来确定化学计量。现在,该技术已广泛用于蛋白质,RNA和各种复合物或纳米结构中的其他大分子的单分子计数。在此,我们以包装噬菌体phi29 DNA的生物马达中的RNA分子计数为例,阐明SMPB技术。此处描述的方法可以应用于其他系统中其他分子的单分子计数。描述了结合棱镜型和物镜型TIRF的简洁,简单,经济的单分子全内反射荧光(TIRF)显微镜的结构。该成像系统包括一个具有单荧光团检测灵敏度的深冷灵敏EMCCD相机,一个用于同时进行双色激发的激光合成器和一个Dual-View 成像器,可将多个结果信号分配给不同的检测器基于它们的波长的通道。描述了用于阐明phi29 DNA包装马达上RNA的化学计量的单分子光漂白测定法的方法,以及蛋白质/ RNA相互作用的机理。审查了单个荧光团标记RNA分子的不同方法。还描述了统计建模的过程,以基于二项式分布揭示生物分子的真实拷贝数。

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