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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2024 · IF 4.3

Design of “Off-On-Off” fluorescence sensors for Heparin detection by precise modulation of molecular structure

Yanan Li,Jian Cao,Chuanxiao Wang,Yiyi Qiao,Jiayu Gao,Xiao Zhang,Le Wang

In this strategy, the fluorescence sensor Nap-Co-T1 employing the fluorescence resonance energy transfer (FRET) mechanism was designed and synthesized to have an efficient response to Heparin, and the FRET mechanism was explored for different excitation-emission wavelengths with different distances between the energy acceptor and the energy donor (comparing with fluorescence sensor Nap-TPA-T2). Upon the addition of Heparin, the fluorescence emission of Nap-Co-T1 was turned on at 565 nm, and the fluorescence color changed of the solution from colorless to bright yellow. The limit of detection (LOD) was as low as 0.04 μg/mL. With the addition of antagonistic protamine (PRTM) to the sensor complex with Heparin, the fluorescence emission was turned off to a certain extent, and the reversibility of the “off-on-off” system was maintained for five cycles or more. In addition, Nap-Co-T1 provides rapid and sensitive detection of Heparin in human serum albumin solution and artificial urine and is highly sensitive to environmental viscosity.

研究领域: 生物化学 · 医学检测
✓ 已验证 DOI PubMed 高影响因子
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY · 2014 · IF 2.129

A dansyl–rhodamine chemosensor for Fe(III) based on off–on FRET

Jingyu Piao,Jia Lv,Xin Zhou,Tong Zhao,Xue Wu

A novel fluorescent chemosensor bearing a rhodamine and a dansyl moiety was developed for highly selective detection of Fe 3+ based on fluorescence resonance energy transfer (FRET) mechanism. Binding of Fe 3+ to the chemosensor induced spirolactam ring opening in the rhodamine moiety and subsequent off–on FRET from the dansyl energy donor to the rhodamine energy acceptor due to the spectral overlap between the emission of the dansyl moiety and the absorption of the ring opened rhodamine moiety. Job’s plot analysis indicated a 1:1 binding stoichiometry between the chemosensor and Fe 3+ . The association constant was estimated to be 2.72   ×   10 3   M −1 according to the Benesi–Hildebrand method. With the feature of easy synthesis, simple structural skeleton and excellent sensing ability, the newly synthesized chemosensor provided the potential for applying as a highly selective fluorescent probe in complex samples containing various competitive metal ions and developing other metal ion chemosensors to fulfill various needs of biological and environmental field.

研究领域: 分析化学 · 生物化学
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CHEMISTRY-A EUROPEAN JOURNAL · 2020 ·Vol. 26 ·期 57 ·13022-13030 · IF 4.857

A Dendron-Based Fluorescence Turn-On Probe for Tumor Detection

Changren Liu,Ling'e Zhang,Sensen Zhou,Xiaoke Zhang,Wei Wu,Xiqun Jiang

Graphical Reductive response : A dendron-based fluorescence turn-on probe mediated by the Förster resonance energy transfer (FRET) mechanism is synthesized by conjugating one Cy5.5 molecule to the focal of a G3 dendron and eight Black Hole Quencher 3 (BHQ-3) molecules to its periphery through a reductively cleavable disulfide linkage. The fluorescence of the probe can be activated effectively and rapidly in the reductive environment of tumors. Specifically amplifying the emission signals of optical probes in tumors is an effective way to improve the tumor-imaging sensitivity and contrast. In this paper, the first case of dendron-based fluorescence turn-on probes mediated by a Förster resonance energy transfer (FRET) mechanism is reported. Dendrons up to the fourth generation with a hydrophilic oligo(ethylene glycol) scaffold are synthesized by a solid-phase synthesis strategy, and show precise and defect-free chemical structures. To construct the fluorescence turn-on probe, one Cy5.5 molecule is conjugated to the focal of a G3 dendron through a robust linkage and eight Black Hole Quencher 3 (BHQ-3) molecules are conjugated to its periphery through a PEG chain bearing a reductively cleavable disulfide linkage. By in vitro and in vivo experiments, it is demonstrated that the fluorescence of the dendron-based probe can be activated effectively and rapidly in the reductive environments of tumor cells and tissues, and the probe thus exhibits amplified tumor signals and weak normal tissue signals. Compared with the reported nanoscale turn-on probes, the dendron-based probe has several significant advantages, such as well-defined chemical structure, precisely controllable fluorophore/quencher conjugation sites and ratio, desirable chemical stability, and reproducible pharmacokinetic and pharmacological profiles, and is very promising in tumor detection.

研究领域: 生物化学 · 医学影像 · 分子生物学
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Materials · 2022 ·Vol. 15 ·期 5 ·1733 · IF 3.748

A Label-Free Fluorescent Sensor Based on Si,N-Codoped Carbon Quantum Dots with Enhanced Sensitivity for the Determination of Cr(VI)

Jinyu Zhang,Cai Jing,Binsong Wang

A signal shut-off probe of Si, N-codoped carbon quantum dots (Si, N-CQDs) was exploited to detect Cr(VI) by fluorescence quenching without the aid of any biomolecules or labeling materials. The sensing system prepared the precursor of diacetone acrylamide and the silane coupling agent 3-aminopropyltriethoxysilane (KH-550) by a simple hydrothermal method, and the quantum yield is as high as 75% Si, N-CQDs. The fluorescence stability and microstructure of the Si, N-CQDs were studied. The Si, N-CQDs has a high sensitivity for detecting Cr(VI) with the linear range of 0–200 μM and the detection limit of 0.995 μM. The quenching mechanism of Si, N-CQDs is attributed to FRET.Keywords:Si,N-codoped carbon quantum dots;hexavalent chromium;fluorescence sensor;mechanism attributed to FRET

研究领域: 分析化学 · 环境科学
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Scientific Reports · 2016 ·Vol. 6 ·期 1 ·1-5 · IF 5.228

An effective colorimetric and ratiometric fluorescent probe based FRET with a large Stokes shift for bisulfite

Wu Wen-Li,Wang Zhao-Yang,Dai Xi,Miao Jun-Ying,Zhao Bao-Xiang

Bisulfite plays crucial roles in diverse physiological processes. Therefore, the efficient detection of bisulfite is very important. In this study, we report a colorimetric and ratiometric fluorescent probe (CPT) with a large Stokes shift (162 nm) for bisulfite (HSO 3 − ) based FRET mechanism. The probe can quantitatively detect HSO 3 − with low detection limit (45 nM) and high specificity over other common anions and biothiols. A nucleophilic addition reaction was proposed for the sensing mechanism, which was confirmed by HRMS spectra. The test strips of the probe were made and used easily. Moreover, probe CPT was used to ratiometric fluorescent imaging of exogenous and endogenous HSO 3 − in living cells.

研究领域: 生物化学 · 分析化学 · 医学检测
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ANALYTICAL CHEMISTRY · 2019 · IF 6.35

Construction of the FRET Pairs for the Visualization of Mitochondria Membrane Potential in Dual Emission Colors

Ruiqing Feng,Lifang Guo,Jinglong Fang,Yue Jia,Xueying Wang,Qin Wei,Xiaoqiang Yu

Mitochondria membrane potential (MMP) play significant roles during metabolism, signaling, and other important bioevents. Visualization of MMP levels is essential for many biological researches. However, fluorescent probes for monitoring MMP levels in dual emission colors are still deficient, which greatly limited the development of relative research areas. In this work, a pair of fluorescent probes have been designed and synthesized to monitor the MMP levels in dual emission colors based on Forster resonance energy transfer (FRET) mechanism. The FRET donor (FixD) is constructed by linking a benzyl chloride group to a fluorophore with bright-green emission. The FixD could target mitochondria and be immobilized in mitochondria by linking to the thiol group of mitochondrial proteins. The FRET acceptor (LA) is designed with green absorption and deep-red emission. In live cells with high MMP levels, FixD and LA both target mitochondria, and deep-red (DR) emission could be detected with the excitation of 405 nm. Particularly, the spectral shift of fluorescence upon the decrease of MMP is up to 110 nm, which is greatly favorable for the clear observation of MMP levels. With the decrease of MMP, LA would be released from mitochondria while FixD would still be immobilized in mitochondria, and decreased DR emission and increased green fluorescence could be detected due to the absence of FRET. In this manner, the MMP levels could be monitored in dual emission colors.

研究领域: 生物化学 · 分子生物学 · 细胞生物学
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ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2022 ·Vol. 414 ·期 9 ·3043-3055 · IF 4.478

A novel fluorescence ratio probe based on dual-emission carbon dots for highly selective and sensitive detection of chlortetracycline and cell imaging

Liang Yu-Qi,Wu Xiao-Yi,Zeng Jia-Yu,Wu Yan-Ni,Lai Jia-Ping,Sun Hui

The novel dual-emission carbon dots (DECDs) for highly selective and sensitive recognition of chlortetracycline (CTC) and cell imaging were synthesized successfully by one-step synthesis. The obtained DECDs possessed two fluorescence peaks (345 nm and 450 nm) and showed specific response to CTC, resulting in a decrease in fluorescence intensity at 345 nm, a blue shift, and an increase in fluorescence intensity at 450 nm. The obtained DECDs exhibited highly selective response to CTC and not to its analogues, such as tetracycline, doxycycline, and oxytetracycline. Thus, an excellent ratiometric probe for the detection of CTC was fabricated successfully and used for the detection of CTC in real samples with the detection limit (LOD) of 16.45 nM. More importantly, the DECDs were used for quantitative detection of CTC in living cells, which demonstrated excellent biocompatibility and broad prospects in biomedicine application. Finally, the excellent selectivity of DECDs toward CTC was attributed to the FRET mechanism and the formation of complexes. Graphical abstract

研究领域: 分析化学 · 生物医学工程 · 材料科学
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ACS Applied Nano Materials · 2024 · IF 5.3

Highly Luminescent and Water-Stable CsPbCl3/Mn2+/PEG Nanocrystals for Ultrasensitive Detection of 4-Nitrophenol

Liming Yang,Yanjun Cui,Bing Hu,Qian Yang,Xia Xu

Perovskite quantum dots (PQDs) offer high photoluminescence quantum yields. However, their poor stability and aqueous-quenching of fluorescence limit their wider application, especially in biochemical detection. In this work, a simple and highly successful coating strategy was used to encapsulate Mn2+-doped CsPbCl3 PQDs in poly(ethylene glycol) (PEG), effectively increasing the water stability of PQDs. After dispersion in deionized water for 25 days, the CsPbCl3/Mn2+/PEG nanocrystals (NCs) retained 40% of their initial fluorescence intensity. In addition, due to the FRET mechanism, 4-nitrophenol (4-NP) can effectively quench the fluorescence of CsPbCl3/Mn2+/PEG NCs. Therefore, utilizing the excellent water stability of CsPbCl3/Mn2+/PEG NCs and their interaction with 4-NP, a fast and conservative fluorescent probe can be established, which can perform highly selective and ultrasensitive quantitative detection of 4-NP in aqueous solutions. In addition, the molecular weight of PEG used for encapsulation, the fluorescence intensity of CsPbCl3/Mn2+/PEG NCs, and the detection range for 4-NP vary. Fortunately, the detection limits are all lower than the drinking water concentrations allowed by the U.S. Environmental Protection Agency. This study also provides a theoretical basis and methodological support for the subsequent application of PQDs in the detection of water pollutants.

CAS / MDL: 25322-68-3
研究领域: 材料科学 · 纳米技术 · 环境科学 · 分析化学
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