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Superresolution Imaging of Targeted Proteins in Fixed and Living Cells Using Photoactivatable Organic Fluorophores

机译:使用光活化有机荧光团对固定和活细胞中的目标蛋白进行超分辨率成像

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摘要

Superresolution imaging techniques based on sequential imaging of sparse subsets of single molecules require fluorophores whose emission can be photoactivated or photoswitched. Because typical organic fluorophores can emit significantly more photons than average fluorescent proteins, organic fluorophores have a potential advantage in super-resolution imaging schemes, but targeting to specific cellular proteins must be provided. We report the design and application of HaloTag-based target-specific azido DCDHFs, a class of photoactivatable push−pull fluorogens which produce bright fluorescent labels suitable for single-molecule superresolution imaging in live bacterial and fixed mammalian cells.
机译:基于单个分子的稀疏子集的顺序成像的超分辨率成像技术需要荧光团,其发射可以被光激活或光切换。因为典型的有机荧光团比普通荧光蛋白能发射更多的光子,所以有机荧光团在超分辨率成像方案中具有潜在的优势,但必须提供针对特定细胞蛋白的靶向。我们报告了基于HaloTag的靶标特定叠氮基DCDHFs的设计和应用,DCDHFs是一类可光激活的推挽式氟,它可产生适用于活细菌和固定哺乳动物细胞的单分子超分辨率成像的明亮荧光标记。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2010年第43期|p.15099-15101|共3页
  • 作者

    Hsiao-lu D. Lee Luc;

  • 作者单位

    Departments of Chemistry, Radiology, Developmental Biology, Stanford University, Stanford, California 94305, and Department of Chemistry, Kent State University, Kent, Ohio 44244;

  • 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);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

  • 入库时间 2022-08-18 00:50:23

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