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Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system

Detection and visualization of phosphates such as ATP in living organisms can facilitate the elucidation of various biological events. Although substantial efforts had been made in this area, present methods have disadvantages such as the need for specialized equipment and poor sensitivities. To add...

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Autores principales: Aoki, Kazusa, Osako, Ryuji, Deng, Jiahui, Hayashita, Takashi, Hashimoto, Takeshi, Suzuki, Yumiko
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/PMC9052313/
https://www.ncbi.nlm.nih.gov/pubmed/35495469
http://dx.doi.org/10.1039/d0ra01455a
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author Aoki, Kazusa
Osako, Ryuji
Deng, Jiahui
Hayashita, Takashi
Hashimoto, Takeshi
Suzuki, Yumiko
author_facet Aoki, Kazusa
Osako, Ryuji
Deng, Jiahui
Hayashita, Takashi
Hashimoto, Takeshi
Suzuki, Yumiko
author_sort Aoki, Kazusa
collection PubMed
description Detection and visualization of phosphates such as ATP in living organisms can facilitate the elucidation of various biological events. Although substantial efforts had been made in this area, present methods have disadvantages such as the need for specialized equipment and poor sensitivities. To address these limitations, novel fluorescent probes, (di-(2-picolyl)amino)quinazolines, were developed for application in ATP detection. They selectively recognized copper ions by fluorescence quenching, and their copper complexes displayed fluorescence enhancement in the presence of phosphoric acid derivatives. This fluorescence on–off system enabled highly sensitive fluorescence detection of ATP when combined with a phenyl boronic acid-modified γ-cyclodextrin through a plausible multipoint recognition system.
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spelling pubmed-90523132022-04-29 Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system Aoki, Kazusa Osako, Ryuji Deng, Jiahui Hayashita, Takashi Hashimoto, Takeshi Suzuki, Yumiko RSC Adv Chemistry Detection and visualization of phosphates such as ATP in living organisms can facilitate the elucidation of various biological events. Although substantial efforts had been made in this area, present methods have disadvantages such as the need for specialized equipment and poor sensitivities. To address these limitations, novel fluorescent probes, (di-(2-picolyl)amino)quinazolines, were developed for application in ATP detection. They selectively recognized copper ions by fluorescence quenching, and their copper complexes displayed fluorescence enhancement in the presence of phosphoric acid derivatives. This fluorescence on–off system enabled highly sensitive fluorescence detection of ATP when combined with a phenyl boronic acid-modified γ-cyclodextrin through a plausible multipoint recognition system. The Royal Society of Chemistry 2020-04-17 /pmc/articles/PMC9052313/ /pubmed/35495469 http://dx.doi.org/10.1039/d0ra01455a Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Aoki, Kazusa
Osako, Ryuji
Deng, Jiahui
Hayashita, Takashi
Hashimoto, Takeshi
Suzuki, Yumiko
Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
title Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
title_full Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
title_fullStr Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
title_full_unstemmed Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
title_short Phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
title_sort phosphate-sensing with (di-(2-picolyl)amino)quinazolines based on a fluorescence on–off system
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9052313/
https://www.ncbi.nlm.nih.gov/pubmed/35495469
http://dx.doi.org/10.1039/d0ra01455a
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