4.7 Article

Raman and SERS microscopy for molecular imaging of live cells

期刊

NATURE PROTOCOLS
卷 8, 期 4, 页码 677-692

出版社

NATURE PUBLISHING GROUP
DOI: 10.1038/nprot.2013.030

关键词

-

资金

  1. JST-ERATO
  2. JST-CREST
  3. JSPS KAKENHI [24710267, 23710276]
  4. Grants-in-Aid for Scientific Research [23710276, 24710267] Funding Source: KAKEN

向作者/读者索取更多资源

Raman microscopy is a promising technology for visualizing the distribution of molecules in cells. A challenge for live-cell imaging using Raman microscopy has been long imaging times owing to the weak Raman signal. Here we present a protocol for constructing and using a Raman microscope equipped with both a slit-scanning excitation and detection system and a laser steering and nanoparticle-tracking system. Slit scanning allows Raman imaging with high temporal and spatial resolution, whereas the laser beam steering system enables dynamic surface-enhanced Raman imaging using gold nanoparticles. Both features enable mapping of the distributions of molecules in live cells and visualization of cellular transport pathways. Furthermore, its utility can be expanded to small-molecule imaging by using tiny Raman-active tags such as alkyne. For example, DNA synthesis in a cell can be visualized by detecting 5-ethynyl-2'-deoxyuridine (EdU), a deoxyuridine derivative with an alkyne moiety. We describe the optics, hardware and software to construct the Raman microscope, and discuss the conditions and parameters involved in live-cell imaging. The whole system can be built in similar to 8 h.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据