Small Fluorogenic Amino Acids for Peptide-Guided Background-Free Imaging
- Angew Chem Int Ed Engl. 2023 Jan 23;62(4):e202216231. doi: 10.1002/anie.202216231.
- 1. Centre for Inflammation Research, The University of Edinburgh, UK.
- 2. EaStCHEM School of Chemistry, The University of Edinburgh, UK.
- 3. Nanoscopy-UGR Laboratory, Facultad de Farmacia, Universidad de Granada, Spain.
- 4. Centre for Clinical Brain Sciences, The University of Edinburgh, UK.
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.
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Cat. No.Product NameDescriptionTargetResearch Area
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target: Amino Acid DerivativesResearch Areas: Others