Shu Dan, Zhang Hui, Jin Jiashun, Guo Peixuan
Department of Comparative Pathobiology and Weldon School of Biomedical Engineering, Purdue University, West Lafayette, IN 47907, USA.
EMBO J. 2007 Jan 24;26(2):527-37. doi: 10.1038/sj.emboj.7601506.
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.
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。