Department of Chemistry, University of Wisconsin-Madison, 1101 University Ave., Madison, WI 53706, USA.
J Bacteriol. 2011 Oct;193(19):5138-46. doi: 10.1128/JB.00198-11. Epub 2011 Jul 22.
By labeling the β' subunit of RNA polymerase (RNAP), we used fluorescence microscopy to study the spatial distribution and diffusive motion of RNAP in live Escherichia coli cells for the first time. With a 40-ms time resolution, the spatial distribution exhibits two or three narrow peaks of 300- to 600-nm full width at half-maximum that maintain their positions within 60 nm over 1 s. The intensity in these features is 20 to 30% of the total. Fluorescence recovery after photobleaching (FRAP) measures the diffusive motion of RNAP on the 1-μm length scale. Averaged over many cells, 53%±19% of the RNAP molecules were mobile on the 3-s timescale, with a mean apparent diffusion constant
通过对 RNA 聚合酶(RNAP)β'亚基进行标记,我们首次使用荧光显微镜研究了活大肠杆菌细胞中 RNAP 的空间分布和扩散运动。在 40 毫秒的时间分辨率下,空间分布呈现出两个或三个半峰全宽为 300-600nm 的狭窄峰,在 1 秒内保持在 60nm 以内的位置。这些特征的强度占总强度的 20-30%。光漂白荧光恢复(FRAP)测量了 RNAP 在 1μm 长度尺度上的扩散运动。在许多细胞的平均值中,53%±19%的 RNAP 分子在 3s 的时间尺度上是可移动的,平均表观扩散常数