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Bright and Light-Up Sensing of Benzo[ c,d ]indole-oxazolopyridine Cyanine Dye for RNA and Its Application to Highly Sensitive Imaging of Nucleolar RNA in Living Cells.

Kei HiguchiYusuke SatoNao TogashiMichiyuki SuzukiYukina YoshinoSeiichi Nishizawa
Published in: ACS omega (2022)
Small molecular weight probes that can show a fluorescence signaling response upon binding to RNAs are promising for RNA imaging in living cells. Live-cell RNA imaging probes that can achieve a large light-up ability (>100-fold) and high Φ bound value for RNA (>0.50) have been rarely reported to date. Here, benzo[ c , d ]indole-oxazolopyridine (BIOP), an unsymmetrical monomethine cyanine analogue, was newly developed as a bright and large light-up probe for imaging of nucleolar RNA in living cells. BIOP served as a yellow-emissive probe (λ em = 570 nm) and exhibited a significant light-up response upon RNA binding (770-fold) with a high Φ bound value (0.52). We demonstrated the advantages of BIOP over a commercially available RNA-staining probe, SYTO RNA select, for robust and sensitive RNA sensing by a systematic comparison of fluorescent properties for RNA. In addition, BIOP was found to possess high membrane permeability and low cytotoxicity in living cells. The examination of live-cell imaging revealed that BIOP exhibited emission in the nucleolus upon binding to nucleolar RNA much stronger than that of SYTO RNA select. Furthermore, BIOP facilitated the highly sensitive imaging of nucleolar RNA, in which 50 nM BIOP can stain nucleolar RNA in living cells with a 20 min incubation.
Keyphrases
  • living cells
  • fluorescent probe
  • single molecule
  • nucleic acid
  • high resolution
  • transcription factor
  • endothelial cells
  • quantum dots
  • binding protein