4.6 Article

A reaction- based near- infrared fluorescent probe that can visualize endogenous selenocysteine in vivo in tumor- bearing mice

Journal

ANALYST
Volume 143, Issue 20, Pages -

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/c8an00765a

Keywords

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Funding

  1. National Natural Science Foundation of China [21502163]
  2. Natural Science Foundation of Jiangsu Province [BK20150206, BK20160022]
  3. Foundation for High-Level Talent in Six Areas of Jiangsu Province [2016-YY-038]
  4. Post-doctoral Fund in Jiangsu Province [1501034B]
  5. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX17_1719]
  6. Jiangsu University Qing Lan Project
  7. Priority Academic Programme Development of Jiangsu Higher Education Institutions (PAPD)

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Monitoring the fluctuations of endogenous selenocysteine (Sec) in vivo is of significant interest to understand the physiological roles of Sec and the mechanisms of Sec-relevant diseases. Herein, a new near-infrared fluorescent probe, Fsec-1, has been developed for the determination of endogenous Sec in living cells and in vivo. Fsec-1 exhibits large fluorescence enhancement (136-fold) and a remarkably large Stokes shift (195 nm) when reacted with Sec. With the advantages of high sensitivity (a detection limit of 10 nM), good selectivity and low cytotoxicity, Fsec-1 was able to recognize both exogenous and endogenous Sec in living cells. The probe was also successfully applied in visualizing both exogenous and endogenous Sec in living mice. Notably, endogenously generated Sec in living tumors xenografted in nude mice was selectively detected by our reaction-based NIR probe for the first time. These results indicated that our new probe could serve as an efficient tool in monitoring endogenous Sec in vivo and exploring the anticancer mechanism of selenium.

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