Construction of a novel aminofluorene-based ratiometric near-infrared fluorescence probe for detecting carboxylesterase activity in living cells

Herein, we constructed a novel aminofluorene-based fluorescence probe ( FEN-CE ) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal. FEN-CE with NIR emission (650 nm) could be hydrolyzed specifically by CE and transformed to FENH with...

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Published inAnalytical methods Vol. 16; no. 23; pp. 3641 - 3645
Main Authors Li, Jun-Mei, Liu, Yan-Zhao, Lv, Xiao-Fang, Zhou, Ding-Heng, Zhang, Hong, Chen, Yu-Jin, Li, Kun
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 13.06.2024
Subjects
Carboxylesterase
Carboxylesterase - analysis
Carboxylesterase - metabolism
Cells (biology)
Emission
Emissions
Fluorenes - chemistry
Fluorescence
Fluorescent Dyes - chemistry
Fluorescent indicators
HeLa Cells
Humans
I.R. radiation
Near infrared radiation
Spectrometry, Fluorescence - methods
Spectroscopy, Near-Infrared - methods
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Abstract Herein, we constructed a novel aminofluorene-based fluorescence probe ( FEN-CE ) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal. FEN-CE with NIR emission (650 nm) could be hydrolyzed specifically by CE and transformed to FENH with the release of the self-immolative group, which exhibited a red-shifted emission peak of 680 nm. In addition, FEN-CE showed high selectivity for CE and was successfully used in the detection of CE activity in living cells through its ratiometric NIR fluorescence signals. Herein, we constructed a novel aminofluorene-based fluorescence probe ( FEN-CE ) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal.
AbstractList Herein, we constructed a novel aminofluorene-based fluorescence probe ( FEN-CE ) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal. FEN-CE with NIR emission (650 nm) could be hydrolyzed specifically by CE and transformed to FENH with the release of the self-immolative group, which exhibited a red-shifted emission peak of 680 nm. In addition, FEN-CE showed high selectivity for CE and was successfully used in the detection of CE activity in living cells through its ratiometric NIR fluorescence signals. Herein, we constructed a novel aminofluorene-based fluorescence probe ( FEN-CE ) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal.
Herein, we constructed a novel aminofluorene-based fluorescence probe (FEN-CE) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal. FEN-CE with NIR emission (650 nm) could be hydrolyzed specifically by CE and transformed to FENH with the release of the self-immolative group, which exhibited a red-shifted emission peak of 680 nm. In addition, FEN-CE showed high selectivity for CE and was successfully used in the detection of CE activity in living cells through its ratiometric NIR fluorescence signals.
Herein, we constructed a novel aminofluorene-based fluorescence probe (FEN-CE) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal. FEN-CE with NIR emission (650 nm) could be hydrolyzed specifically by CE and transformed to FENH with the release of the self-immolative group, which exhibited a red-shifted emission peak of 680 nm. In addition, FEN-CE showed high selectivity for CE and was successfully used in the detection of CE activity in living cells through its ratiometric NIR fluorescence signals.Herein, we constructed a novel aminofluorene-based fluorescence probe (FEN-CE) for the detection of carboxylesterase (CE) in living cells by a ratiometric near-infrared (NIR) fluorescence signal. FEN-CE with NIR emission (650 nm) could be hydrolyzed specifically by CE and transformed to FENH with the release of the self-immolative group, which exhibited a red-shifted emission peak of 680 nm. In addition, FEN-CE showed high selectivity for CE and was successfully used in the detection of CE activity in living cells through its ratiometric NIR fluorescence signals.
Author Li, Kun
Li, Jun-Mei
Zhang, Hong
Chen, Yu-Jin
Liu, Yan-Zhao
Lv, Xiao-Fang
Zhou, Ding-Heng
AuthorAffiliation College of Chemistry
Key Laboratory of Green Chemistry and Technology of Ministry of Education
Sichuan University
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CitedBy_id crossref_primary_10_1016_j_ccr_2025_216480
crossref_primary_10_1016_j_jphotochem_2024_116005
Cites_doi 10.1038/nrd3373
10.1039/C5SC05001D
10.1016/j.talanta.2020.121744
10.1016/j.snb.2020.128798
10.1002/anie.202101190
10.1016/j.talanta.2019.120143
10.1016/j.dyepig.2022.110079
10.1016/j.talanta.2020.121098
10.1039/C7CC00577F
10.1016/j.dyepig.2021.109993
10.1016/j.talanta.2020.121307
10.1016/j.bios.2022.114392
10.1038/nrd2468
10.31635/ccschem.021.202100985
10.1039/C9CC05759E
10.1016/j.snb.2022.131779
10.1039/C8QM00107C
10.1021/acssensors.0c02398
10.1016/j.biomaterials.2017.08.026
10.1021/acs.analchem.8b05417
10.1039/D0TB02673E
10.1039/C9CS00243J
10.1016/j.foodchem.2023.137062
10.1016/j.snb.2019.127567
10.1039/D2TB00422D
10.1039/C7CS00862G
10.1371/journal.pone.0049515
10.1016/j.dyepig.2022.110549
10.1016/j.dyepig.2020.108345
10.1039/C5CC08764C
10.1038/s41467-017-02270-0
10.1021/acs.molpharmaceut.1c00761
10.1016/j.aca.2021.339248
10.1021/acssensors.0c01734
10.1021/acsami.8b11365
10.1021/acsanm.3c05917
10.1021/acssensors.8b00697
10.1021/jo502213t
10.1002/anie.202009796
10.1021/jacs.7b07748
10.1021/acs.analchem.0c01554
10.1016/S1359-6446(05)03383-0
10.1021/acs.analchem.9b04189
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References Horváth (D4AY00501E/cit38/1) 2015; 80
Wang (D4AY00501E/cit18/1) 2020; 5
Tian (D4AY00501E/cit14/1) 2019; 91
Halabi (D4AY00501E/cit23/1) 2017; 139
Dai (D4AY00501E/cit43/1) 2021; 223
Jiang (D4AY00501E/cit13/1) 2019; 55
Steffes (D4AY00501E/cit8/1) 2017; 145
Wu (D4AY00501E/cit36/1) 2020; 219
Tian (D4AY00501E/cit21/1) 2019; 91
Zhao (D4AY00501E/cit3/1) 2024; 7
Hu (D4AY00501E/cit29/1) 2018; 2
Quiroga (D4AY00501E/cit6/1) 2012; 7
Wang (D4AY00501E/cit37/1) 2020; 306
Guo (D4AY00501E/cit20/1) 2022; 199
Redinbo (D4AY00501E/cit4/1) 2005; 10
Li (D4AY00501E/cit12/1) 2021; 60
Shen (D4AY00501E/cit15/1) 2020; 178
Levine (D4AY00501E/cit27/1) 2016; 52
Wu (D4AY00501E/cit26/1) 2021; 60
Rautio (D4AY00501E/cit5/1) 2008; 7
Park (D4AY00501E/cit34/1) 2020; 49
Dong (D4AY00501E/cit32/1) 2022; 205
Ma (D4AY00501E/cit22/1) 2020; 325
Li (D4AY00501E/cit1/1) 2019; 205
Li (D4AY00501E/cit17/1) 2022; 362
Zhang (D4AY00501E/cit41/1) 2021; 6
Zhang (D4AY00501E/cit10/1) 2022; 19
Pang (D4AY00501E/cit35/1) 2020; 217
Luo (D4AY00501E/cit2/1) 2024; 430
Kepp (D4AY00501E/cit7/1) 2011; 10
Liu (D4AY00501E/cit19/1) 2022; 211
Wang (D4AY00501E/cit30/1) 2018; 10
Xiang (D4AY00501E/cit42/1) 2022; 10
Hu (D4AY00501E/cit33/1) 2018; 9
Liu (D4AY00501E/cit25/1) 2020; 92
Liu (D4AY00501E/cit11/1) 2018; 47
Zhang (D4AY00501E/cit31/1) 2022; 198
Yang (D4AY00501E/cit39/1) 2017; 53
Yin (D4AY00501E/cit16/1) 2022; 1190
Park (D4AY00501E/cit24/1) 2016; 7
Zhang (D4AY00501E/cit28/1) 2021; 9
Liu (D4AY00501E/cit40/1) 2018; 3
Zhuang (D4AY00501E/cit9/1) 2021; 4
References_xml – volume: 10
  start-page: 221
  year: 2011
  ident: D4AY00501E/cit7/1
  publication-title: Nat. Rev. Drug Discovery
  doi: 10.1038/nrd3373
– volume: 7
  start-page: 3703
  year: 2016
  ident: D4AY00501E/cit24/1
  publication-title: Chem. Sci.
  doi: 10.1039/C5SC05001D
– volume: 223
  start-page: 121744
  year: 2021
  ident: D4AY00501E/cit43/1
  publication-title: Talanta
  doi: 10.1016/j.talanta.2020.121744
– volume: 325
  start-page: 128798
  year: 2020
  ident: D4AY00501E/cit22/1
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2020.128798
– volume: 60
  start-page: 15418
  year: 2021
  ident: D4AY00501E/cit26/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.202101190
– volume: 205
  start-page: 120143
  year: 2019
  ident: D4AY00501E/cit1/1
  publication-title: Talanta
  doi: 10.1016/j.talanta.2019.120143
– volume: 199
  start-page: 110079
  year: 2022
  ident: D4AY00501E/cit20/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2022.110079
– volume: 217
  start-page: 121098
  year: 2020
  ident: D4AY00501E/cit35/1
  publication-title: Talanta
  doi: 10.1016/j.talanta.2020.121098
– volume: 53
  start-page: 3952
  year: 2017
  ident: D4AY00501E/cit39/1
  publication-title: Chem. Commun.
  doi: 10.1039/C7CC00577F
– volume: 198
  start-page: 109993
  year: 2022
  ident: D4AY00501E/cit31/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2021.109993
– volume: 219
  start-page: 121307
  year: 2020
  ident: D4AY00501E/cit36/1
  publication-title: Talanta
  doi: 10.1016/j.talanta.2020.121307
– volume: 211
  start-page: 114392
  year: 2022
  ident: D4AY00501E/cit19/1
  publication-title: Biosens. Bioelectron.
  doi: 10.1016/j.bios.2022.114392
– volume: 7
  start-page: 255
  year: 2008
  ident: D4AY00501E/cit5/1
  publication-title: Nat. Rev. Drug Discovery
  doi: 10.1038/nrd2468
– volume: 4
  start-page: 1028
  year: 2021
  ident: D4AY00501E/cit9/1
  publication-title: CCS Chem.
  doi: 10.31635/ccschem.021.202100985
– volume: 55
  start-page: 11358
  year: 2019
  ident: D4AY00501E/cit13/1
  publication-title: Chem. Commun.
  doi: 10.1039/C9CC05759E
– volume: 362
  start-page: 131779
  year: 2022
  ident: D4AY00501E/cit17/1
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2022.131779
– volume: 2
  start-page: 1201
  year: 2018
  ident: D4AY00501E/cit29/1
  publication-title: Mater. Chem. Front.
  doi: 10.1039/C8QM00107C
– volume: 6
  start-page: 1138
  year: 2021
  ident: D4AY00501E/cit41/1
  publication-title: ACS Sens.
  doi: 10.1021/acssensors.0c02398
– volume: 145
  start-page: 242
  year: 2017
  ident: D4AY00501E/cit8/1
  publication-title: Biomaterials
  doi: 10.1016/j.biomaterials.2017.08.026
– volume: 91
  start-page: 5638
  year: 2019
  ident: D4AY00501E/cit21/1
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.8b05417
– volume: 9
  start-page: 2457
  year: 2021
  ident: D4AY00501E/cit28/1
  publication-title: J. Mater. Chem. B
  doi: 10.1039/D0TB02673E
– volume: 49
  start-page: 143
  year: 2020
  ident: D4AY00501E/cit34/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C9CS00243J
– volume: 430
  start-page: 137062
  year: 2024
  ident: D4AY00501E/cit2/1
  publication-title: Food Chem.
  doi: 10.1016/j.foodchem.2023.137062
– volume: 306
  start-page: 127567
  year: 2020
  ident: D4AY00501E/cit37/1
  publication-title: Sens. Actuators, B
  doi: 10.1016/j.snb.2019.127567
– volume: 10
  start-page: 4254
  year: 2022
  ident: D4AY00501E/cit42/1
  publication-title: J. Mater. Chem. B
  doi: 10.1039/D2TB00422D
– volume: 47
  start-page: 7140
  year: 2018
  ident: D4AY00501E/cit11/1
  publication-title: Chem. Soc. Rev.
  doi: 10.1039/C7CS00862G
– volume: 7
  start-page: e49515
  year: 2012
  ident: D4AY00501E/cit6/1
  publication-title: PLoS One
  doi: 10.1371/journal.pone.0049515
– volume: 205
  start-page: 110549
  year: 2022
  ident: D4AY00501E/cit32/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2022.110549
– volume: 178
  start-page: 108345
  year: 2020
  ident: D4AY00501E/cit15/1
  publication-title: Dyes Pigm.
  doi: 10.1016/j.dyepig.2020.108345
– volume: 52
  start-page: 1835
  year: 2016
  ident: D4AY00501E/cit27/1
  publication-title: Chem. Commun.
  doi: 10.1039/C5CC08764C
– volume: 9
  start-page: 362
  year: 2018
  ident: D4AY00501E/cit33/1
  publication-title: Nat. Commun.
  doi: 10.1038/s41467-017-02270-0
– volume: 19
  start-page: 630
  year: 2022
  ident: D4AY00501E/cit10/1
  publication-title: Mol. Pharmaceutics
  doi: 10.1021/acs.molpharmaceut.1c00761
– volume: 1190
  start-page: 339248
  year: 2022
  ident: D4AY00501E/cit16/1
  publication-title: Anal. Chim. Acta
  doi: 10.1016/j.aca.2021.339248
– volume: 5
  start-page: 3264
  year: 2020
  ident: D4AY00501E/cit18/1
  publication-title: ACS Sens.
  doi: 10.1021/acssensors.0c01734
– volume: 10
  start-page: 31088
  year: 2018
  ident: D4AY00501E/cit30/1
  publication-title: ACS Appl. Mater. Interfaces
  doi: 10.1021/acsami.8b11365
– volume: 7
  start-page: 5252
  year: 2024
  ident: D4AY00501E/cit3/1
  publication-title: ACS Appl. Nano Mater.
  doi: 10.1021/acsanm.3c05917
– volume: 3
  start-page: 2118
  year: 2018
  ident: D4AY00501E/cit40/1
  publication-title: ACS Sens.
  doi: 10.1021/acssensors.8b00697
– volume: 80
  start-page: 1299
  year: 2015
  ident: D4AY00501E/cit38/1
  publication-title: J. Org. Chem.
  doi: 10.1021/jo502213t
– volume: 60
  start-page: 17268
  year: 2021
  ident: D4AY00501E/cit12/1
  publication-title: Angew. Chem., Int. Ed.
  doi: 10.1002/anie.202009796
– volume: 139
  start-page: 13200
  year: 2017
  ident: D4AY00501E/cit23/1
  publication-title: J. Am. Chem. Soc.
  doi: 10.1021/jacs.7b07748
– volume: 92
  start-page: 9205
  year: 2020
  ident: D4AY00501E/cit25/1
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.0c01554
– volume: 10
  start-page: 313
  year: 2005
  ident: D4AY00501E/cit4/1
  publication-title: Drug Discovery Today
  doi: 10.1016/S1359-6446(05)03383-0
– volume: 91
  start-page: 15840
  year: 2019
  ident: D4AY00501E/cit14/1
  publication-title: Anal. Chem.
  doi: 10.1021/acs.analchem.9b04189
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Snippet Herein, we constructed a novel aminofluorene-based fluorescence probe ( FEN-CE ) for the detection of carboxylesterase (CE) in living cells by a ratiometric...
Herein, we constructed a novel aminofluorene-based fluorescence probe (FEN-CE) for the detection of carboxylesterase (CE) in living cells by a ratiometric...
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SubjectTerms Carboxylesterase
Carboxylesterase - analysis
Carboxylesterase - metabolism
Cells (biology)
Emission
Emissions
Fluorenes - chemistry
Fluorescence
Fluorescent Dyes - chemistry
Fluorescent indicators
HeLa Cells
Humans
I.R. radiation
Near infrared radiation
Spectrometry, Fluorescence - methods
Spectroscopy, Near-Infrared - methods
Title Construction of a novel aminofluorene-based ratiometric near-infrared fluorescence probe for detecting carboxylesterase activity in living cells
URI https://www.ncbi.nlm.nih.gov/pubmed/38812419
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https://www.proquest.com/docview/3062534187
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