Zhang Hui, Shu Dan, Huang Faqing, Guo Peixuan
Department of Comparative Pathobiology, Purdue University, West Lafayette, Indiana 47907, USA.
RNA. 2007 Oct;13(10):1793-802. doi: 10.1261/rna.587607. Epub 2007 Aug 13.
Limited by the spatial resolution of optical microscopy, direct detection or counting of single components in biological complexes or nanoparticles is challenging, especially for RNA, which is conformationally versatile and structurally flexible. We report here the assembly of a customized single-molecule dual-viewing total internal reflection fluorescence imaging system for direct counting of RNA building blocks. The RNA molecules were labeled with a single fluorophore by in vitro transcription in the presence of a fluorescent AMP. Precise calculation of identical or mixed pRNA building blocks of one, two, three, or six copies within the bacteriophage phi29 DNA packaging motor or other complexes was demonstrated by applying a photobleaching assay and evaluated by binomial distribution. The dual-viewing system for excitation and recording at different wavelengths simultaneously will enable the differentiation of different complexes with different labels or relative motion of each labeled component in motion machines.
受光学显微镜空间分辨率的限制,直接检测或计数生物复合物或纳米颗粒中的单个成分具有挑战性,尤其是对于RNA而言,因为RNA具有多种构象且结构灵活。我们在此报告了一种定制的单分子双视角全内反射荧光成像系统的组装,用于直接计数RNA构建块。通过在荧光AMP存在下进行体外转录,RNA分子用单个荧光团标记。通过应用光漂白测定法证明了在噬菌体phi29 DNA包装马达或其他复合物中精确计算一、二、三或六个拷贝的相同或混合pRNA构建块,并通过二项分布进行评估。同时在不同波长下进行激发和记录的双视角系统将能够区分具有不同标记的不同复合物或运动机器中每个标记成分的相对运动。