4.8 Article

All-Optical Wide-Field Selective Imaging of Fluorescent Nanodiamonds in Cells, In Vivo and Ex Vivo

期刊

ACS NANO
卷 15, 期 8, 页码 12869-12879

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.0c07740

关键词

D color centers; nanomaterials; nanoparticles; bioimaging; HeLa cells; C. elegans; rat hippocampus

资金

  1. MEXT Quantum Leap Flagship Program (MEXT Q-LEAP) [JPMXS0120330644]
  2. Japan Science and Technology Agency under Precursory Research for Embryonic Science and Technology (PRESTO) [JPMJPR14F1, JPMJPR18G1]
  3. MEXT Japan
  4. JSPS KAKENHI [JP20H02587, JP20H00453, JP18H06501, JP20K19969, JP18K11916, JP18K18839, JP17H01262, JP18H02483, JP21H02532]
  5. PRIME from Japan Agency for Medical Research and Development [JP19gm6110022h001]
  6. MEXT QLEAP Grant [JPMXS0118067395]
  7. CAO Public/Private R&D Investment Strategic Expansion PrograM (CAO PRISM)
  8. AMED [JP21zf0127004]
  9. NIH Office of Research Infrastructure Programs [P40 OD010440]

向作者/读者索取更多资源

The method described in this study utilizes controlled laser pulses to oscillate the fluorescence from nitrogen-vacancy centers (NVCs) in fluorescent nanodiamonds, while oscillating other optical signals in the opposite phase. This allows for the reconstruction of selective images of nanodiamonds with improved signal-to-background ratio, providing a powerful tool for investigating molecular dynamics in cells and in vivo.
Fluorescence imaging is a critical tool to understand the spatial distribution of biomacromolecules in cells and in vivo, providing information on molecular dynamics and interactions. Numerous valuable insights into biological systems have been provided by the specific detection of various molecular species. However, molecule-selective detection is often hampered by background fluorescence, such as cell autofluorescence and fluorescence leakage from molecules stained by other dyes. Here we describe a method for all-optical selective imaging of fluorescent nanodiamonds containing nitrogen-vacancy centers (NVCs) for wide-field fluorescence bioimaging. The method is based on the fact that the fluorescence intensity of NVCs strictly depends on the configuration of ground-state electron spins, which can be controlled by changing the pulse recurrence intervals of microsecond excitation laser pulses. Therefore, by using regulated laser pulses, we can oscillate the fluorescence from NVCs in a nanodiamond, while oscillating other optical signals in the opposite phase to NVCs. As a result, we can reconstruct a selective image of a nanodiamond by using a series of oscillated fluorescence images. We demonstrate application of the method to the selective imaging of nanodiamonds in live cells, in microanimals, and on a hippocampal slice culture obtained from a rat. Our approach potentially enables us to achieve high-contrast images of nanodiamond-labeled biomolecules with a signal-to-background ratio improved by up to 100-fold over the standard fluorescence image, thereby providing a more powerful tool for the investigation of molecular dynamics in cells and in vivo.

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