Tang Wei, Newton Ronald J, Xie Chang An, Li Yong Qing, Whitley Nicki
Department of Biology, Howell Science Complex, East Carolina University, Greenville, NC 27858-4353, USA.
Genomics Proteomics Bioinformatics. 2005 Aug;3(3):169-78. doi: 10.1016/s1672-0229(05)03022-6.
Transgenic cell lines of loblolly pine (Pinus taeda L.) were analyzed by a compact laser-tweezers-Raman-spectroscopy (LTRS) system in this investigation. A low power diode laser at 785 nm was used for both laser optical trapping of single transgenic cells and excitation for near-infrared Raman spectroscopy of the nuclei of synchronized cells, which were treated as single organic particles, at the S-phase of the cell cycle. Transgenic living cells with gfp and uidA genes were used as biological samples to test this LTRS technique. As expected, different Raman spectra were observed from the tested biological samples. This technique provides a high sensitivity and enables real-time spectroscopic measurements of transgenic cell lines. It could be a valuable tool for the study of the fundamental cell and molecular biological process by trapping single nucleus and by providing a wealth of molecular information about the nuclei of cells.
在本研究中,利用紧凑型激光镊子拉曼光谱(LTRS)系统对火炬松(Pinus taeda L.)的转基因细胞系进行了分析。使用波长为785 nm的低功率二极管激光器,对单个转基因细胞进行激光光学捕获,并对处于细胞周期S期的同步化细胞的细胞核进行近红外拉曼光谱激发,这些细胞被视为单个有机颗粒。携带gfp和uidA基因的转基因活细胞被用作生物样本,以测试这种LTRS技术。正如预期的那样,从测试的生物样本中观察到了不同的拉曼光谱。该技术具有高灵敏度,能够对转基因细胞系进行实时光谱测量。通过捕获单个细胞核并提供有关细胞核的大量分子信息,它可能成为研究基本细胞和分子生物学过程的宝贵工具。