Department of Bioengineering, The University of Tokyo, Tokyo, Japan.
J Biotechnol. 2012 Dec 15;164(2):254-9. doi: 10.1016/j.jbiotec.2012.08.006. Epub 2012 Aug 30.
In this study, we used the homologous recombination protein RecA to locate a specific sequence on DNA. Single-stranded (ss) DNA (80-mer, 5'-biotinylated), complementary to the sequence of interest, was labeled with quantum dots (Qdots(®)) via biotin-avidin binding. The DNA was then mixed with RecA to form a fluorescent-labeled ssDNA-RecA complex. λ DNA, which was used as the target DNA, was stretch-and-positioned onto microelectrodes by using the electrostatic method. When the ssDNA-RecA complex was fed to the suspended target DNA, clear fluorescence spots were observed on individual target DNA molecules. The histogram of the probe-binding position along the target DNA was measured, and the peak was found to correspond to the location complementary to the probe ssDNA. This result shows a potential use for recombination proteins in facilitating the optical detection of DNA sequences.
在这项研究中,我们使用同源重组蛋白 RecA 来定位 DNA 上的特定序列。通过生物素-亲和素结合,将与感兴趣的序列互补的单链 DNA(80 -mer,5′-生物素化)标记上量子点(Qdots(®))。然后,将 DNA 与 RecA 混合形成荧光标记的 ssDNA-RecA 复合物。将 λ DNA 用作靶 DNA,通过静电方法将其拉伸并定位到微电极上。当将 ssDNA-RecA 复合物供给悬浮的靶 DNA 时,可以在单个靶 DNA 分子上观察到清晰的荧光点。测量了探针结合位置沿靶 DNA 的直方图,发现峰对应于与探针 ssDNA 互补的位置。该结果表明重组蛋白在促进 DNA 序列的光学检测方面具有潜在的用途。