4.8 Article

Acid-Resistant BODIPY Amino Acids for Peptide-Based Fluorescence Imaging of GPR54 Receptors in Pancreatic Islets

Journal

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
Volume 62, Issue 20, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202302688

Keywords

Diabetes; Fluorescence; GPCRs; Probes; Solid-Phase Peptide Synthesis

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This study describes the rational design and characterization of a new acid-resistant BODIPY-based amino acid (Trp-BODIPY PLUS) and its application in solid-phase synthesis of fluorescent bioactive peptides. The amino acid retains the binding capabilities of both short linear and cyclic peptides and shows notable turn-on fluorescence emission upon target binding for wash-free imaging. Trp-BODIPY PLUS was used to prepare fluorogenic kisspeptin-based probes and visualize the expression and localization of GPR54 receptors in human cells and whole mouse pancreatic islets by fluorescence imaging.
The G protein-coupled kisspeptin receptor (GPR54 or KISS1R) is an important mediator in reproduction, metabolism and cancer biology; however, there are limited fluorescent probes or antibodies for direct imaging of these receptors in cells and intact tissues, which can help to interrogate their multiple biological roles. Herein, we describe the rational design and characterization of a new acid-resistant BODIPY-based amino acid (Trp-BODIPY PLUS), and its implementation for solid-phase synthesis of fluorescent bioactive peptides. Trp-BODIPY PLUS retains the binding capabilities of both short linear and cyclic peptides and displays notable turn-on fluorescence emission upon target binding for wash-free imaging. Finally, we employed Trp-BODIPY PLUS to prepare some of the first fluorogenic kisspeptin-based probes and visualized the expression and localization of GPR54 receptors in human cells and in whole mouse pancreatic islets by fluorescence imaging.

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