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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...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Royal Society of Chemistry
2020
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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. |
format | Online Article Text |
id | pubmed-9053952 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | The Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
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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