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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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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
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author Sharma, Neha
Barbon, Stephanie M.
Lalonde, Tyler
Maar, Ryan R.
Milne, Mark
Gilroy, Joe B.
Luyt, Leonard G.
author_facet Sharma, Neha
Barbon, Stephanie M.
Lalonde, Tyler
Maar, Ryan R.
Milne, Mark
Gilroy, Joe B.
Luyt, Leonard G.
author_sort Sharma, Neha
collection PubMed
description 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.
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spelling pubmed-90539522022-05-04 The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents Sharma, Neha Barbon, Stephanie M. Lalonde, Tyler Maar, Ryan R. Milne, Mark Gilroy, Joe B. Luyt, Leonard G. RSC Adv Chemistry 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. The Royal Society of Chemistry 2020-05-19 /pmc/articles/PMC9053952/ /pubmed/35518290 http://dx.doi.org/10.1039/d0ra02104k Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Sharma, Neha
Barbon, Stephanie M.
Lalonde, Tyler
Maar, Ryan R.
Milne, Mark
Gilroy, Joe B.
Luyt, Leonard G.
The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
title The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
title_full The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
title_fullStr The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
title_full_unstemmed The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
title_short The development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
title_sort development of peptide–boron difluoride formazanate conjugates as fluorescence imaging agents
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053952/
https://www.ncbi.nlm.nih.gov/pubmed/35518290
http://dx.doi.org/10.1039/d0ra02104k
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