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Non-destructive Analysis of the Nuclei of Transgenic Living Cells Using Laser Tweezers and Near-infrared Raman Spectroscopic Technique

机译:激光镊子和近红外拉曼光谱技术对转基因活细胞核的无损分析

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摘要

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.
机译:在这项研究中,通过紧凑的激光镊子-拉曼光谱(LTRS)系统分析了火炬松(Pinus taeda L.)的转基因细胞系。 785 nm的低功率二极管激光器既用于单个转基因细胞的激光光学捕获,又用于激发同步细胞核的近红外拉曼光谱,该同步细胞在细胞的S相被视为单个有机颗粒。周期。具有gfp和uidA基因的转基因活细胞被用作生物学样品,以测试该LTRS技术。如预期的那样,从测试的生物样品中观察到不同的拉曼光谱。这项技术具有很高的灵敏度,并可以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,它可能是研究基本细胞和分子生物学过程的有价值的工具。

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