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使用定制的单分子双视图系统对 phi29 DNA 包装马达的六种原核 RNA 进行计数。

Counting of six pRNAs of phi29 DNA-packaging motor with customized single-molecule dual-view system.

作者信息

Shu Dan, Zhang Hui, Jin Jiashun, Guo Peixuan

机构信息

Department of Comparative Pathobiology and Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.

出版信息

EMBO J. 2007 Jan 24;26(2):527-37. doi: 10.1038/sj.emboj.7601506.

Abstract

Direct imaging or counting of RNA molecules has been difficult owing to its relatively low electron density for EM and insufficient resolution in AFM. Bacteriophage phi29 DNA-packaging motor is geared by a packaging RNA (pRNA) ring. Currently, whether the ring is a pentagon or hexagon is under fervent debate. We report here the assembly of a highly sensitive imaging system for direct counting of the copy number of pRNA within this 20-nm motor. Single fluorophore imaging clearly identified the quantized photobleaching steps from pRNA labeled with a single fluorophore and concluded its stoichiometry within the motor. Almost all of the motors contained six copies of pRNA before and during DNA translocation, identified by dual-color detection of the stalled intermediates of motors containing Cy3-pRNA and Cy5-DNA. The stalled motors were restarted to observe the motion of DNA packaging in real time. Heat-denaturation analysis confirmed that the stoichiometry of pRNA is the common multiple of 2 and 3. EM imaging of procapsid/pRNA complexes clearly revealed six ferritin particles that were conjugated to each pRNA ring.

摘要

由于RNA分子的电子密度相对较低,不利于进行电子显微镜(EM)成像,且在原子力显微镜(AFM)中的分辨率不足,因此对RNA分子进行直接成像或计数一直很困难。噬菌体phi29 DNA包装马达由一个包装RNA(pRNA)环驱动。目前,关于该环是五边形还是六边形存在激烈争论。我们在此报告了一种高灵敏度成像系统的组装,用于直接计数这个20纳米马达内pRNA的拷贝数。单荧光团成像清楚地识别了单个荧光团标记的pRNA的量子化光漂白步骤,并确定了其在马达内的化学计量。通过对含有Cy3-pRNA和Cy5-DNA的马达停滞中间体进行双色检测,几乎所有马达在DNA转运之前和期间都含有六个pRNA拷贝。使停滞的马达重新启动,以实时观察DNA包装的运动。热变性分析证实,pRNA的化学计量是2和3的公倍数。原衣壳/pRNA复合物的EM成像清楚地显示了与每个pRNA环结合的六个铁蛋白颗粒。

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