Small Fluorogenic Amino Acids for Peptide-Guided Background-Free Imaging.
Fabio de MolinerZuzanna KoniecznaLorena Mendive-TapiaRebecca S SaleebKatie MorrisJuan Antonio Gonzalez-VeraTakeshi KaizukaSeth G N GrantMathew H HorrocksMarc VendrellPublished in: Angewandte Chemie (Weinheim an der Bergstrasse, Germany) (2022)
The multiple applications of super-resolution microscopy have prompted the need for minimally invasive labeling strategies for peptide-guided fluorescence imaging. Many fluorescent reporters display limitations (e.g., large and charged scaffolds, non-specific binding) as building blocks for the construction of fluorogenic peptides. Herein we have built a library of benzodiazole amino acids and systematically examined them as reporters for background-free fluorescence microscopy. We have identified amine-derivatized benzoselenadiazoles as scalable and photostable amino acids for the straightforward solid-phase synthesis of fluorescent peptides. Benzodiazole amino acids retain the binding capabilities of bioactive peptides and display excellent signal-to-background ratios. Furthermore, we have demonstrated their application in peptide-PAINT imaging of postsynaptic density protein-95 nanoclusters in the synaptosomes from mouse brain tissues.
Keyphrases
- amino acid
- fluorescence imaging
- high resolution
- label free
- single molecule
- minimally invasive
- quantum dots
- photodynamic therapy
- living cells
- gene expression
- optical coherence tomography
- mass spectrometry
- binding protein
- energy transfer
- sensitive detection
- dna binding
- tissue engineering
- small molecule
- single cell
- transcription factor