Pyrene excimer possesses a large Stokes shift and long fluorescence lifetime and has been widely applied in developing time-resolved biosensing systems to solve the autofluorescence interference problems in biological samples. However, only a few of pyrene excimer-based small molecular probes have been reported so far. Ratiometric probes, on the other hand, can eliminate interferences from environmental factors such as instrumental efficiency and environmental conditions by a built-in correction of the dual emission bands but are ineffective for endogenous autofluorescence in biosystems. In this work, by combining the advantages of time-resolved fluorescence technique with ratiometric probe, we reported a bispyrene-fluorescein hybrid FRET cassette (PF) as a novel ratiometric time-resolved sensing platform for bioanalytical applications, with pH chosen as a biorelated target. The probe PF showed a fast, highly selective, and reversible ratiometric fluorescence response to pH in a wide range from 3.0 to 10.0 in buffered solution. By employing time-resolved fluorescence technique, the pH-induced fluorescence signal of probe PF can be well-discriminated from biological autofluorescence background, which enables us to detect pH in a range of 4.0-8.0 in cell media within a few seconds. It has also been preliminarily applied for ratiometric quantitative monitoring of pH changes in living cells with satisfying results. Since many fluorescein-based fluorescence probes have been developed, our strategy might find wide applications in design ratiometric time-resolved probes for detection of various biorelated targets.
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http://dx.doi.org/10.1021/ac502863m | DOI Listing |
Anal Chem
December 2024
Department of Pharmacy, Zhongnan Hospital of Wuhan University, School of Pharmaceutical Sciences, Wuhan University, Wuhan 430071, China.
A ratiometric fluorescence-photothermal dual-mode assay method is constructed for the detection of butyrylcholinesterase (BChE) activity based on time-resolved levodopa (L-DOPA) cascade polymerization. First, a newly designed bimetallic metal-organic framework (MOF), Eu/Co-DPA (DPA: pyridine-2,6-dicarboxylic acid), is screened out as a fluorescent nanozyme with high catalytic activity and superior luminescence properties. In the presence of boric acid (BA), L-DOPA forms BA-esterified L-DOPA, which is catalyzed by Eu/Co-DPA to form the oligomers with strong blue fluorescence.
View Article and Find Full Text PDFNat Plants
November 2024
State Key Laboratory of Crop Stress Biology for Arid Areas and College of Life Sciences, Northwest Agriculture & Forestry University, Yangling, China.
Abscisic acid (ABA) regulates plant stress adaptation, growth and reproduction. Despite extensive ABA-Ca signalling links, imaging ABA-induced increases in Ca concentration has been challenging, except in guard cells. Here we visualize ABA-triggered [Ca] dynamics in diverse organs and cell types of Arabidopsis thaliana using a genetically encoded Ca ratiometric sensor with a low-nanomolar Ca-binding affinity and a large dynamic range.
View Article and Find Full Text PDFDalton Trans
October 2024
Department of Chemistry, Wayne State University, Detroit, MI 48202, USA.
BaFCl:Eu,Tb nanocrystals were synthesized hot-injection thermolysis of metal chlorodifluoroacetates and their luminescence response characterized between 80 and 430 K. Though unintended, partial reduction of Eu to Eu occurred during the synthesis stage, leading to luminescent nanocrystals coactivated by Eu, Eu, and Tb. Their emission was dominated by Eu, specifically by radiative transitions 4f (P) → 4f (S) and 4f5d (lowest level) → 4f (S).
View Article and Find Full Text PDFChemosphere
September 2024
College of Chemistry and Chemical Engineering, State Key Laboratory of Chemical Safety, China University of Petroleum, Qingdao, 266580, China. Electronic address:
The assessment of perfluorooctanoic acid (PFOA) photocatalytic degradation usually involves tedious pre-treatment and sophisticated instrumentation, making it impractical to evaluate the degradation process in real-time. Herein, we synthesized a series of lanthanide metal-organic frameworks (Ln-MOFs) with outstanding fluorescent sensing properties and applied them as luminescent probes in the photocatalytic degradation reaction of PFOA for real-time evaluation. As the catalytic reaction proceeds, the fluorescence color changes significantly from green to orange-red due to the different interaction mechanisms between the electron-deficient PFOA and smaller radius F with the ratiometric fluorescent probe MOF-76 (Tb: Eu = 29:1).
View Article and Find Full Text PDFPhys Chem Chem Phys
July 2024
Department of Chemistry, University of Calcutta, 92, A.P.C. Road, Kolkata, 700009, India.
The present study describes photophysical properties of 3-(benzo[]oxazol-2-yl)-5-bromo-2-hydroxybenzaldehyde (HBOB) and ()-2-(benzo[]oxazol-2-yl)-4-bromo-6-(hydrazonomethyl)phenol (HBON) molecules with asymmetric two-way proton transfer sites. The purpose of this study is to know the direction of ESIPT out of the two-way proton transfer pathways in these molecules in both the solid and solution state. The steady state and time-resolved spectral behaviour of HBOB and HBON and a comparison of the spectral features with the two distinct control compounds 2-(benzo[]oxazol-2-yl)-4-bromophenol (HBO) and ()-4-bromo-2-(hydrazonomethyl)phenol (HBN) having single 6-membered hydrogen bonded network reveal that HBOB undergoes imine-amine photoisomerisation by proton transfer towards the oxazole side and HBON undergoes towards the hydrazone side with characteristic Stokes' shifted emission.
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