Rhodamine-based near-infrared probe for emission detection of ATP in lysosomes in living cells

Anjong Florence Tikum; Gyoungmi Kim; Azam Nasirian; Jeong Won Ko; Juyoung Yoon; Jinheung Kim

doi:10.1016/j.snb.2019.04.112

Rhodamine-based near-infrared probe for emission detection of ATP in lysosomes in living cells

Anjong Florence Tikum, Gyoungmi Kim, Azam Nasirian, Jeong Won Ko, Juyoung Yoon, Jinheung Kim

Chemistry & Nanoscience

Research output: Contribution to journal › Article › peer-review

28 Scopus citations

Abstract

A new near infrared fluorescent probe was designed and prepared to detect ATP and target lysosomes in cells. The non-fluorescent probe was turned on during the interaction with ATP, affording a 115-fold increase in fluorescence intensity. The colorless probe turned purple upon interaction with ATP. The probe displayed high sensitivity and selectivity toward ATP compared with other biomolecules, such as AMP, ADP, GMP, and CMP. Such significant spectroscopic changes derive from a structural change of the probe's spirocyclic moiety to its ring-opened form. This occurs through electrostatic and π,π-stacking interactions between the probe and ATP. This probe was also used in selective lysosome staining and for real-time ATP level monitoring. It exhibits great advantages in cell imaging studies, such as excellent photostability, low cytotoxicity, and good cell membrane permeability.

Original language	English
Pages (from-to)	40-47
Number of pages	8
Journal	Sensors and Actuators, B: Chemical
Volume	292
DOIs	https://doi.org/10.1016/j.snb.2019.04.112
State	Published - 1 Aug 2019

Bibliographical note

Funding Information:
This work was supported by the National Research Foundation (NRF) grant funded by the Korean government ( NRF-2017R1A5A1015365 ) and “Next Generation Carbon Upcycling Project” (Project No. 2017M1A2A2046740) through the NRF funded by the Ministry of Science and ICT . J.Y. acknowledges grants from the National Creative Research Initiative programs of the National Research Foundation of Korea (NRF) funded by the Korean government (MSIP) (No. 2012R1A3A2048814 ). Mass spectral data were obtained from the Korea Basic Science Institute (Daegu), by Jeol JMS 700 high-resolution mass spectrometry.

Publisher Copyright:
© 2019 Elsevier B.V.

Keywords

Adenosine triphosphate
Cell imaging
Fluorescence detection
Fluorescent probe for ATP
Lysosome targeting

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10.1016/j.snb.2019.04.112

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title = "Rhodamine-based near-infrared probe for emission detection of ATP in lysosomes in living cells",

abstract = "A new near infrared fluorescent probe was designed and prepared to detect ATP and target lysosomes in cells. The non-fluorescent probe was turned on during the interaction with ATP, affording a 115-fold increase in fluorescence intensity. The colorless probe turned purple upon interaction with ATP. The probe displayed high sensitivity and selectivity toward ATP compared with other biomolecules, such as AMP, ADP, GMP, and CMP. Such significant spectroscopic changes derive from a structural change of the probe's spirocyclic moiety to its ring-opened form. This occurs through electrostatic and π,π-stacking interactions between the probe and ATP. This probe was also used in selective lysosome staining and for real-time ATP level monitoring. It exhibits great advantages in cell imaging studies, such as excellent photostability, low cytotoxicity, and good cell membrane permeability.",

keywords = "Adenosine triphosphate, Cell imaging, Fluorescence detection, Fluorescent probe for ATP, Lysosome targeting",

author = "Tikum, {Anjong Florence} and Gyoungmi Kim and Azam Nasirian and Ko, {Jeong Won} and Juyoung Yoon and Jinheung Kim",

note = "Funding Information: This work was supported by the National Research Foundation (NRF) grant funded by the Korean government ( NRF-2017R1A5A1015365 ) and “Next Generation Carbon Upcycling Project” (Project No. 2017M1A2A2046740) through the NRF funded by the Ministry of Science and ICT . J.Y. acknowledges grants from the National Creative Research Initiative programs of the National Research Foundation of Korea (NRF) funded by the Korean government (MSIP) (No. 2012R1A3A2048814 ). Mass spectral data were obtained from the Korea Basic Science Institute (Daegu), by Jeol JMS 700 high-resolution mass spectrometry. Publisher Copyright: {\textcopyright} 2019 Elsevier B.V.",

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AU - Yoon, Juyoung

AU - Kim, Jinheung

N1 - Funding Information: This work was supported by the National Research Foundation (NRF) grant funded by the Korean government ( NRF-2017R1A5A1015365 ) and “Next Generation Carbon Upcycling Project” (Project No. 2017M1A2A2046740) through the NRF funded by the Ministry of Science and ICT . J.Y. acknowledges grants from the National Creative Research Initiative programs of the National Research Foundation of Korea (NRF) funded by the Korean government (MSIP) (No. 2012R1A3A2048814 ). Mass spectral data were obtained from the Korea Basic Science Institute (Daegu), by Jeol JMS 700 high-resolution mass spectrometry. Publisher Copyright: © 2019 Elsevier B.V.

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N2 - A new near infrared fluorescent probe was designed and prepared to detect ATP and target lysosomes in cells. The non-fluorescent probe was turned on during the interaction with ATP, affording a 115-fold increase in fluorescence intensity. The colorless probe turned purple upon interaction with ATP. The probe displayed high sensitivity and selectivity toward ATP compared with other biomolecules, such as AMP, ADP, GMP, and CMP. Such significant spectroscopic changes derive from a structural change of the probe's spirocyclic moiety to its ring-opened form. This occurs through electrostatic and π,π-stacking interactions between the probe and ATP. This probe was also used in selective lysosome staining and for real-time ATP level monitoring. It exhibits great advantages in cell imaging studies, such as excellent photostability, low cytotoxicity, and good cell membrane permeability.

AB - A new near infrared fluorescent probe was designed and prepared to detect ATP and target lysosomes in cells. The non-fluorescent probe was turned on during the interaction with ATP, affording a 115-fold increase in fluorescence intensity. The colorless probe turned purple upon interaction with ATP. The probe displayed high sensitivity and selectivity toward ATP compared with other biomolecules, such as AMP, ADP, GMP, and CMP. Such significant spectroscopic changes derive from a structural change of the probe's spirocyclic moiety to its ring-opened form. This occurs through electrostatic and π,π-stacking interactions between the probe and ATP. This probe was also used in selective lysosome staining and for real-time ATP level monitoring. It exhibits great advantages in cell imaging studies, such as excellent photostability, low cytotoxicity, and good cell membrane permeability.

KW - Adenosine triphosphate

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KW - Fluorescence detection

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Rhodamine-based near-infrared probe for emission detection of ATP in lysosomes in living cells

Abstract

Bibliographical note

Keywords

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