4.4 Article

Chloro-Functionalized Photo-crosslinking BODIPY for Glutathione Sensing and Subcellular Trafficking

Journal

CHEMBIOCHEM
Volume 19, Issue 10, Pages 1001-1005

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/cbic.201800059

Keywords

dyes; pigments; fluorescence; imaging agents; photochemistry; sensors

Funding

  1. KIST [CAP-16-02-KIST, CAP-17-01-KISTEurope]
  2. Ministry of Science, ICT & Future Planning [NRF-2016M3A9B6902060, NRF-2017M3A9D8029942, 2015H1D3A1036045]
  3. National Research Council of Science & Technology (NST), Republic of Korea [CAP-17-01-KISTEUROPE] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
  4. National Research Foundation of Korea [2015H1D3A1036045] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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Glutathione (GSH) is one of major antioxidants inside cells that regulates oxidoreduction homeostasis. Recently, there have been extensive efforts to visualize GSH in live cells, but most of the probes available today are simple detection sensors and do not provide details of cellular localization. A new fluorescent probe (pcBD2-Cl), which is cell permeable and selectively reacts with GSH in situ, has been developed. The in situ GSH-labeled probe (pcBD2-GSH) exhibited quenches fluorescence, but subsequent binding to cellular abundant glutathione S-transferase (GST) recovers the fluorescence intensity, which makes it possible to image the GSH-GST complex in live cells. Interactions between probe and GST were confirmed by means of photo-crosslinking under intact live-cell conditions. Interestingly, isomers of chloro-functionalized 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene (BODIPY) compounds behaved very distinctively inside the cells. Following co-staining imaging with MitoTracker and mitochondria fractionation upon lipopolysaccharide-mediated reactive oxygen species induction experiments showed that pcBD2-GSH accumulated in mitochondria. This is the first example of a live-cell imaging probe to visualize translocation of GSH from the cytosol to mitochondria.

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