4.7 Article

A tumor-targeting near-infrared fluorescent probe for real-time imaging ATP in cancer cells and mice

Journal

ANALYTICA CHIMICA ACTA
Volume 1206, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.aca.2022.339798

Keywords

Fluorescent probe; Adenosine triphosphate; Tumor-targeting; Near-infrared image

Funding

  1. National Natural Science Foundation of China [22174122, 21775133]
  2. Hunan Provincial Natural Science Foundation [2021JJ30654]
  3. Scientific Research Fund of Hunan Provincial Education Department [21A0084, 19A479]
  4. Open Research Fund of School of Chemistry and Chemical Engineering, Henan Normal University [2020YB01]
  5. Key Project of Science and Technology of Henan Province [202102310215]
  6. Degree & Postgraduate Education Reform Project of Hunan Province [2019JGYB113]
  7. Hunan Provincial Innovation Foundation For Postgraduate [CX20190483, CX20200635, XDCX2020B115]

Ask authors/readers for more resources

Adenosine triphosphate (ATP) is crucial for cellular energy, and its abnormal metabolism is linked to various diseases. Developing a tumor-targeting fluorescent probe for imaging ATP is essential for understanding its role in cancer. Bio-SiR, a NIR fluorescent probe, shows good selectivity and targeting ability for ATP imaging in cancer cells.
Adenosine triphosphate (ATP) is an important biomolecule, which is the primary source of cellular energy. In particular, an abnormal metabolism of ATP level has been took part in many diseases, such as cancer. Thus, developing an effective fluorescent probe for tumor-targeting imaging of ATP is great importance for in-depth understanding the functions of ATP in tumor invasion and matastasis. In this work, we present the design and synthesis of a tumor-targeting near-infrared (NIR) fluorescent probe named Bio-SiR. Bio-SiR is mainly composed of three parts: si-rhodamine-based fluorophore, diethylenetriamine-based recognition group and biotin-based tumor-targetable group. When Bio-SiR reacts with ATP, a turn-on fluorescence at 675 nm (NIR region) is observed clearly, which is suitable for its application in mice. In addition, due to a concurrent effect from dual recognition sites, the probe Bio-SiR displays excellent selectivity for ATP over other potential biological analytes. Under the guidance of biotin group, Bio-SiR can be successfully used for imaging ATP in cancer cells. Furthermore, live-cell imaging allows us to directly real-time monitor the dynamic change of ATP in cancer cells. In particular, this is the first tumor-targeting NIR small-molecule fluorescent probe for endogenous ATP imaging in tumor-bearing mice. These features demonstrate that this probe is a useful imaging tool for expounding the function of ATP in cancer. (c) 2022 Elsevier B.V. All rights reserved.

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