De novo formation of citrate-based fluorophores on N-termini of peptides and proteins in cells and tissues. Issue 1 (2nd December 2019)

• Record Type: Journal Article
• Authors: Jung, Dongwook; Choi, Dongkil; Sim, Changgon; Kim, Yumin; Kang, Sunyoung; Nam, So Hee; Jang, Joomyung; Kim, Dokyoung; Chang, Mee Soo; Park, Ji-Ung; Lee, Yan
• Is Part Of: Chemical communications. Volume 56:Issue 1(2020)
• Page Start: 74
• Page End: 77
• Publication Date: 2019-12-02
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c9cc08494k
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : Citrate-based fluorophores are generated in de novo manner on proteins in biological samples under mild conditions. Abstract : We developed a new method for the de novo formation of fluorophores based on citrate (DNFC) in biological samples. Use of an amide coupling reagent and microwave irradiation greatly facilitates the fluorophore formation on peptides and proteins with N-terminal cysteine or serine. Since N-terminal cysteine and serine can form thiazolopyridone- or oxazolopyridone-based fluorophores emitting blue and green fluorescence, respectively, by the DNFC staining, each organelle, cell and tissue exhibited a characteristic fluorescence distribution. The DNFC staining is able to provide a new potential protocol for future cell imaging, histology and diagnosis.