Abstract
BODIPY-linked bithiophene-tetrazoles were designed and synthesized for bioorthogonal photoclick reactions in vitro and in vivo. The reactivity of these tetrazoles toward dimethyl fumarate was found to depend on the BODIPY attachment site, with the meta-linked BODIPY–tetrazole being the most reactive. The resulting pyrazoline cycloadduct showed drastically reduced BODIPY fluorescence. However, BODIPY fluorescence recovered after treatment with hydrogen peroxide. This turn-on effect was attributed to conversion from the pyrazoline to a pyrazole. Finally, we showed that this unique BODIPY–tetrazole off–on fluorescence probe can be used to detect hydrogen peroxide inside HeLa cells.
| Original language | English |
|---|---|
| Pages (from-to) | 1326-1333 |
| Number of pages | 8 |
| Journal | ChemBioChem |
| Volume | 19 |
| Issue number | 12 |
| DOIs | |
| State | Published - Jun 18 2018 |
Keywords
- bioorthogonal
- BODIPY
- fluorescent probes
- hydrogen peroxide
- tetrazole
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