4.8 Article

Localizable and Photoactivatable Fluorophore for Spatiotemporal Two-Photon Bioimaging

期刊

ANALYTICAL CHEMISTRY
卷 87, 期 11, 页码 5626-5631

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.analchem.5b00691

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资金

  1. National Key Scientific Program of China [2011CB911000]
  2. NSFC [21325520, 21327009, 21375076, J1210040, 21177036, 21135001]
  3. Foundation for Innovative Research Groups of NSFC [21221003]
  4. National Instrumentation Program [2011YQ030124]
  5. Hunan Provincial Natural Science Foundation [11JJ1002]

向作者/读者索取更多资源

Photoactivatable probe-based fluorescent imaging has become an efficient and attractive technique for spatiotemporal microscopic studies of biological events. However, almost all previously reported photoactivatable organic probes have been based on hydrosoluble precursors, which have produced water-soluble active fluorophores able to readily diffuse away from the photocleavage site, thereby dramatically reducing spatial resolution. Hydroxyphenylquinazolinone (HPQ), a small organic dye known for its classic luminescence mechanism through excited-state intramolecular proton transfer (ESIPT), shows strong light emission in the solid state, but no emission in solution. In this work, HPQ was employed as a precursor to develop a localizable, photoactivatable two-photon probe (PHPQ) for spatiotemporal bioimaging applications. After photocleavage, PHPQ releases a precipitating HPQ fluorophore which shows both one-photon and two-photon excited yellow-green fluorescence, thereby producing a localizable fluorescence signal that affords high spatial resolution for bioimaging, with more than 200-fold one-photon and 150-fold two-photon fluorescence enhancement.

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