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The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents

Two new fluorescence imaging probes have been synthesized by incorporating a versatile alkyne-substituted boron difluoride formazanate precursor with peptides through copper-catalyzed alkyne–azide cycloaddition. The formazanate dye was appended to a C-terminal amino acid of ghrelin for imaging the g...

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Detalles Bibliográficos
Autores principales: Sharma, Neha, Barbon, Stephanie M., Lalonde, Tyler, Maar, Ryan R., Milne, Mark, Gilroy, Joe B., Luyt, Leonard G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053952/
https://www.ncbi.nlm.nih.gov/pubmed/35518290
http://dx.doi.org/10.1039/d0ra02104k
Descripción
Sumario:Two new fluorescence imaging probes have been synthesized by incorporating a versatile alkyne-substituted boron difluoride formazanate precursor with peptides through copper-catalyzed alkyne–azide cycloaddition. The formazanate dye was appended to a C-terminal amino acid of ghrelin for imaging the growth hormone secretagogue receptor (GHSR-1a). To demonstrate versatile bioconjugation chemistry, the formazanate dye was added to the N-terminus of bombesin for targeting the gastrin releasing peptide receptor (GRPR). These are the first examples of using this emerging class of dyes, boron difluoride formazanates, for the labelling of biomolecules.