Small Fluorogenic Amino Acids for Peptide-Guided Background-Free Imaging

被引:0
|
作者
de Moliner, Fabio [1 ]
Konieczna, Zuzanna [2 ]
Mendive-Tapia, Lorena [1 ]
Saleeb, Rebecca S. [2 ]
Morris, Katie [2 ]
Gonzalez-Vera, Juan Antonio [3 ]
Kaizuka, Takeshi [4 ]
Grant, Seth G. N. [4 ]
Horrocks, Mathew H. [2 ]
Vendrell, Marc [1 ]
机构
[1] Univ Edinburgh, Ctr Inflammat Res, Edinburgh, Scotland
[2] Univ Edinburgh, EaStCHEM Sch Chem, Edinburgh, Scotland
[3] Univ Granada, Fac Farm, Nanoscopy UGR Lab, Granada, Spain
[4] Univ Edinburgh, Ctr Clin Brain Sci, Edinburgh, Scotland
基金
英国生物技术与生命科学研究理事会; 欧洲研究理事会; 英国惠康基金;
关键词
Fluorescence; Microscopy; Probes; Proteins; Super-Resolution; SUPERRESOLUTION MICROSCOPY; FLUORESCENT PROTEINS; FLUOROPHORE; CELLS; LOCALIZATION; NANOSCALE; MOLECULES;
D O I
10.1002/anie.202216231
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
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页数:8
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