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Rapid confocal Raman imaging using a synchro multifoci-scan scheme for dynamic monitoring of single living cells

机译:使用同步多焦点扫描方案进行快速共聚焦拉曼成像,以动态监测单个活细胞

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摘要

We developed a rapid multifoci-scan confocal Raman microscopy system for label-free molecular imaging of single living cells. A pair of galvo-mirrors were used to raster scan a single laser to generate multifoci excitations and another galvo-mirror synchronously projected Raman scattering from each foci onto a multichannel spectrograph such that multiple spectra were collected simultaneously. The image acquisition time is ~40 times faster than in conventional point-scan Raman microscopy with diffraction-limited resolution retained. We demonstrated that this system can be used to monitor the germination dynamics of single bacterial spores with about 1.0 min resolution and 2.5 mW power at each focal point.
机译:我们开发了一种快速的多焦点扫描共聚焦拉曼显微镜系统,用于单个活细胞的无标记分子成像。一对振镜用于光栅扫描单个激光器以产生多焦点激发,另一个振镜将来自每个焦点的拉曼散射同步投影到多通道光谱仪上,以便同时收集多个光谱。图像采集时间是传统点扫描拉曼显微镜的40倍,保留了衍射极限分辨率。我们证明了该系统可用于监测每个焦点处约1.0分钟的分辨率和2.5 mW功率的单个细菌孢子的萌发动态。

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  • 来源
    《Applied Physics Letters》 |2011年第21期|p.213703.1-213703.3|共3页
  • 作者单位

    Department of Physics, East Carolina University, Greenville, North Carolina 27858-4353, USA;

    Department of Physics, East Carolina University, Greenville, North Carolina 27858-4353, USA;

    Department of Physics, East Carolina University, Greenville, North Carolina 27858-4353, USA;

    Department of Molecular, Microbial and Structural Biology, University of Connecticut Health Center,Farmington, Connecticut 06030-3305, USA;

    Department of Physics, East Carolina University, Greenville, North Carolina 27858-4353, USA;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);
  • 原文格式 PDF
  • 正文语种 eng
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