ABSTRACT
Superior photostability, minimal phototoxicity, red-shifted absorption/emission wavelengths, high brightness, and an enlarged Stokes shift are essential characteristics of top-tier organic fluorophores, particularly for long-lasting super-resolution imaging in live cells (e.g., via stimulated emission depletion (STED) nanoscopy). However, few existing fluorophores possess all of these properties. In this study, we demonstrate a general approach for simultaneously enhancing these parameters through the introduction of 9,9-dimethyl-9,10-dihydroacridine (DMA) as an electron-donating auxochrome. DMA not only induces red shifts in emission wavelengths but also suppresses photooxidative reactions and prevents the formation of triplet states in DMA-based fluorophores, greatly improving photostability and remarkably minimizing phototoxicity. Moreover, the DMA group enhances the fluorophores' brightness and enlarges the Stokes shift. Importantly, the "universal" benefits of attaching the DMA auxochrome have been exemplified in various fluorophores including rhodamines, difluoride-boron complexes, and coumarin derivatives. The resulting fluorophores successfully enabled the STED imaging of organelles and HaloTag-labeled membrane proteins.
Subject(s)
Fluorescent Dyes , Humans , Rhodamines , Microscopy, Fluorescence/methods , HeLa Cells , IonophoresABSTRACT
Ferroptosis is an iron-dependent programmed cell death that is characterized by the dysregulation of lipid reactive oxygen species (ROS) production, causing abnormal changes in hypochlorous acid (HClO) levels in lysosomes. Super-resolution imaging can observe the fine structure of the lysosome at the nanometer level; therefore, it can be used to detect lysosome HClO levels during ferroptosis at the suborganelle level. Herein, we utilize a ratiometric fluorescent probe, SRF-HClO, for super-resolution imaging of lysosome HClO. Structured-illumination microscopy (SIM) improves the accuracy of lysosome targeting and enables the probe SRF-HClO to be successfully applied to rapidly monitor the up-regulated lysosome HClO at the nanoscale during inflammation and ferroptosis. Importantly, the probe SRF-HClO can also detect HClO changes in inflammatory and ferroptosis mice and evaluate the inhibitory effect of ferroptosis on mice tumors.
Subject(s)
Ferroptosis , Fluorescent Dyes , Hypochlorous Acid , Lysosomes , Ferroptosis/drug effects , Fluorescent Dyes/chemistry , Hypochlorous Acid/analysis , Hypochlorous Acid/metabolism , Lysosomes/chemistry , Lysosomes/metabolism , Animals , Mice , Humans , Optical Imaging , RAW 264.7 CellsABSTRACT
5,10-Dimethyl-5,10-dihydrophenazine (MP) is utilized as an effective auxochrome, leveraging its highly conjugated structure to enhance the photophysical and photochemical properties of fluorophores. As illustrated in the difluoride-boron complex and coumarin fluorophores, the extensive conjugation of MP auxochrome substantially red-shifts the absorption/emission wavelengths and increases Stokes shift due to the intensified intramolecular charge transfer effect; notably, MP auxochrome effectively improves fluorophores' photostability by mitigating photooxidative reactions through enhanced electron density delocalization on nitrogen atoms and increased ionization potential. Importantly, MP-based fluorophores demonstrate applicability in stimulated emission depletion nanomicroscopy, showcasing their utility in lipid droplet labeling.
ABSTRACT
Tumor microenvironment-responsive phototheranostic agents are highly sought after for their ability to improve diagnostic accuracy and treatment specificity. Here, we introduce a novel single-molecule probe, POZ-NO, which is activated by nitric oxide (NO) and weak acidity, enabling dual-mode imaging and photothermal therapy (PTT) of tumors. In acidic environments with elevated NO levels, POZ-NO exhibits a distinctive ratiometric fluorescence signal shift from the red to near-infrared, accompanied by a 700 nm photoacoustic signal. Additionally, POZ-NO demonstrated potent photothermal effects upon NO and acidity activation, achieving an impressive conversion efficiency of 74.3% under 735 nm laser irradiation. In vivo studies confirm POZ-NO's ability to accurately image tumors through ratiometric fluorescence and photoacoustic modes while selectively treating tumors with PTT.
Subject(s)
Nitric Oxide , Photoacoustic Techniques , Photothermal Therapy , Tumor Microenvironment , Nitric Oxide/analysis , Nitric Oxide/metabolism , Nitric Oxide/chemistry , Animals , Humans , Mice , Optical Imaging , Hydrogen-Ion Concentration , Theranostic Nanomedicine , Mice, Inbred BALB C , Female , Fluorescent Dyes/chemistry , FluorescenceABSTRACT
For the first time, three acceptor-donor-acceptor (A-D-A)-type boranil fluorescent dyes, CSU-BF-R (R = H, CH3, and OCH3), featuring phenothiazine as the donor, were designed and synthesized. CSU-BF-R exhibited remarkable photophysical characteristics, including large Stokes shifts (>150 nm), high fluorescence quantum yields (up to 40%), long-wavelength emissions, and strong red solid-state fluorescence. Moreover, these CSU-BF-R fluorescent dyes were demonstrated to function as highly selective and sensitive ratiometric fluorescent probes for detecting hypochlorous acid (HClO). The preliminary biological applications of CSU-BF-OCH3 for sensing intracellular HClO in living cells and zebrafish were demonstrated. Therefore, CSU-BF-R possess the potential to further explore the physiological and pathological functions associated with HClO and provide valuable insights into the design of high-performance A-D-A-type fluorescent dyes.
Subject(s)
Drug Design , Fluorescent Dyes , Hypochlorous Acid , Zebrafish , Fluorescent Dyes/chemistry , Fluorescent Dyes/chemical synthesis , Animals , Hypochlorous Acid/analysis , Hypochlorous Acid/chemistry , Humans , Aniline Compounds/chemistry , Aniline Compounds/chemical synthesis , Molecular Structure , Optical ImagingABSTRACT
Intracellular redox homeostasis is highly important for the physiological processes of living organisms. Real-time monitoring of the dynamics of this intracellular redox process is pivotal but challenging because the biological redox reactions involved in the process are reversible and require at least one pair of oxidizing and reducing species. Thus, biosensors for investigating intracellular redox homeostasis need to be dual-functional, reversible, and, ideally, ratiometric in order for them to have real-time monitoring capacity and to provide accurate imaging information. In light of the importance of the redox pair between ClO- and GSH in living organisms, herein, we used the phenoselenazine (PSeZ) moiety as an electron donor and a reaction site to design a coumarin-based fluorescent probe, PSeZ-Cou-Golgi. After successive treatment with ClO- and GSH, the probe PSeZ-Cou-Golgi experienced an oxidation of selenium (Se) to selenoxide (SeâO) by ClO- and a subsequent reduction of SeâO to Se by GSH. The redox reactions alternatively changed the electron-donating strength of the donor in the probe PSeZ-Cou-Golgi, in turn affecting the intramolecular charge transfer process that resulted in the reversible, ratiometric change of fluorescence from red to green. After four cycles of reversible ClO-/GSH detection during in vitro experiments, the probe PSeZ-Cou-Golgi still had good performance. With the Golgi-targeting group, the probe PSeZ-Cou-Golgi was able to monitor the dynamic change of the ClO-/GSH-mediated redox state during Golgi oxidative stress, making it a versatile molecular tool. More importantly, the probe PSeZ-Cou-Golgi could facilitate the imaging of the dynamic redox state during acute lung injury progression.
Subject(s)
Fluorescent Dyes , Selenium , Oxidation-Reduction , Oxidative Stress , Diagnostic Imaging , HomeostasisABSTRACT
Rhodamines have emerged as a useful class of dye for bioimaging. However, intrinsic issues such as short emission wavelengths and small Stokes shifts limit their widespread applications in living systems. By taking advantage of the homoadamantane-fused tetrahydroquinoxaline (HFT) moiety as an electron donor, we developed a new class of asymmetric NIR rhodamine dyes, NNR1-7. These new dyes retained ideal photophysical properties from the classical rhodamine scaffold and showed large Stokes shifts (>80 nm) with improved chemo/photostability. We found that NNR1-7 specifically target cellular mitochondria with superior photobleaching resistance and improved tolerance for cell fixation compared to commercial mitochondria trackers. Based on NNR4, a novel NIR pH sensor (NNR4M) was also constructed and successfully applied for real-time monitoring of variations in lysosomal pH. We envision this design strategy would find broad applications in the development of highly stable NIR dyes with a large Stokes shift.
Subject(s)
Electrons , Fluorescent Dyes , Rhodamines/chemistry , Fluorescent Dyes/chemistry , LysosomesABSTRACT
Nonalcoholic fatty liver disease (NAFLD) can progress to cirrhosis and liver cancer if left untreated. Therefore, it is of great importance to develop useful tools for the noninvasive and accurate diagnosis of NAFLD. Increased microenvironmental viscosity was considered as a biomarker of NAFLD, but the occurrence of increased viscosity in other liver diseases highly reduces the diagnosis accuracy of NAFLD by a single detection of viscosity. Hence, it is very necessary to seek a second biomarker of NAFLD. It has been innovatively proposed that the overexpressed heme oxygenase-1 enzyme in NAFLD would produce abnormally high concentrations of CO in hepatocytes and that CO could serve as a potential biomarker. In this work, we screened nine lactam Changsha dyes (HCO-1-HCO-9) with delicate structures to obtain near-infrared (NIR), metal-free, and "dual-locked" fluorescent probes for the simultaneous detection of CO and viscosity. Changsha dyes with a 2-pyridinyl hydrazone substituent could sense CO, and the 5-position substituents on the 2-pyridinyl moiety had a great electron effect on the reaction rate. The double bond in these dyes served as the sensing group for viscosity. Probe HCO-9 was utilized for precise diagnosis of NAFLD by simultaneous detection of CO and viscosity. Upon reacting with CO in a high-viscosity microenvironment, strong fluorescence at 745 nm of probe HCO-9 was turned on with NIR excitation at 700 nm. Probe HCO-9 was proven to be an effective tool for imaging CO and viscosity. Due to the advantages of NIR absorption and low toxicity, probe HCO-9 was successfully applied to image NAFLD in a mouse model.
Subject(s)
Non-alcoholic Fatty Liver Disease , Mice , Animals , Non-alcoholic Fatty Liver Disease/diagnostic imaging , Fluorescent Dyes/chemistry , Carbon Monoxide , Viscosity , BiomarkersABSTRACT
Mitochondrial dysfunction is associated with increased viscosity and reactive oxygen species (ROS) levels. As an effective antioxidant, sulfur dioxide (SO2) can actively scavenge excess ROS to regulate the redox state and protect cells from oxidative stress. However, few studies have evaluated the connection between viscosity and SO2 during mitochondrial dysfunction. Herein, a water-soluble fluorescent probe (MBI) is designed and synthesized for dual-detecting SO2 and viscosity. The probe rapidly detects SO2 within 12 s based on Michael's addition reaction. Meanwhile, increasing viscosity further inhibits the intramolecular rotation, causing the probe to show a greatly enhanced fluorescence. Probe MBI possesses mitochondria targeting capability due to its quaternary ammonium salt. More importantly, probe MBI successfully supports SO2 and viscosity imaging in living cells and can effectively monitor them during mitochondrial dysfunction and cell apoptosis.
Subject(s)
Fluorescent Dyes , Sulfur Dioxide , Humans , Reactive Oxygen Species , Viscosity , Solubility , HeLa Cells , Mitochondria , WaterABSTRACT
Idiopathic pulmonary fibrosis (IPF) is a chronic, progressive, and fatal interstitial pneumonia with unknown pathogenesis. Early diagnosis and therapeutic intervention are essential for improving the prognosis of patients with IPF. The level of nitric oxide upregulates in the alveoli of IPF patients, which is correlated with the severity of the disease. Herein, we report a fluorescent probe DCM-nitric oxide (NO) to detect IPF by monitoring the concentration changes of NO. This probe displays a fast response time and a good linear response to NO in vitro. Fluorescence imaging experiments with probe DCM-NO revealed that the level of intracellular NO increases in the pulmonary fibrosis cells and IPF mice models. Probe DCM-NO displayed a strong red fluorescence in IPF mice models. However, a declining fluorescence was evidenced in the OFEV-treated IPF mice, implying that DCM-NO is capable of evaluating the therapeutic effects on IPF. Thus, probe DCM-NO can quickly predict the progression of pulmonary fibrosis at an early stage and thus help improve the effective treatment.
Subject(s)
Idiopathic Pulmonary Fibrosis , Animals , Fluorescent Dyes/therapeutic use , Humans , Idiopathic Pulmonary Fibrosis/diagnostic imaging , Idiopathic Pulmonary Fibrosis/drug therapy , Mice , Nitric Oxide , Optical Imaging , Pulmonary Alveoli/pathologyABSTRACT
Based on the selective ClO--triggered chlorination reaction and the subsequent pKa decrease of phenols, a new strategy was developed for rationally designing ratiometric ClO- fluorescent probes with high selectivity. By investigating the fluorescence responses of 6-cyano-2-naphthol toward ClO- and the pKa-dependent response mechanism, we developed a rapid, sensitive and selective two-photon ratiometric fluorescent probe, Naph-DFOB, to detect ClO-. This probe displayed a ratiometric fluorescence change (from 509 nm to 628 nm) toward ClO- and was successfully applied to image intracellular ClO- in living cells with two-photon excitation. Using Naph-DFOB as a useful tool, the investigation of lipopolysaccharide (LPS)-induced acute lung injury in a mouse model was effectively performed.
Subject(s)
Fluorescent Dyes , Hypochlorous Acid , Mice , Animals , Fluorescent Dyes/toxicity , Halogenation , Photons , FluorescenceABSTRACT
Benzopyrylium-coumarin fluorescent probes for sensing hypochlorous acid (HClO) or sulfur dioxide (SO2) are unable to distinguish between HClO and SO2 because the two compounds can react with the 4-position of benzopyrylium-coumarin dyes through the nucleophilic attack. In the current work, we introduced a phenoxazine moiety to the benzopyrylium-coumarin dye to synthesize a new fluorescent probe PBC1, which can dually sense HClO and SO2 and generate distinct fluorescence signals with rapid response time and high sensitivity and selectivity. Moreover, probe PBC1 was also successfully utilized to detect intracellular HClO and SO2 in HeLa cells and zebrafish.
Subject(s)
Hypochlorous Acid , Zebrafish , Animals , Coumarins , Fluorescence , Fluorescent Dyes , HeLa Cells , Humans , Sulfur DioxideABSTRACT
For better investigating the complicated relationships between H2S and SO2, simultaneously detecting and visualizing them with good selectivity is crucial. However, most sensing mechanisms for H2S and SO2 probes are based on the addition reactions with the double bonds, which have no selectivity. In this work, by introducing an active triple bond into 4-dicyanovinyl-7-diethylamino-coumarin, we construct two unique sensors for not only distinguishing between H2S and SO2 but also sensing H2S and SO2 in a dual-ratiometric manner. Moreover, the modified sensor was successfully applied in living cells and zebrafish for discriminating H2S and SO2.
Subject(s)
Fluorescent Dyes , Hydrogen Sulfide , Animals , HeLa Cells , Humans , Sulfur Dioxide , ZebrafishABSTRACT
The ratiometric detection of cysteine (Cys) and homocysteine (Hcy) is very challenging because of their highly similar chemical structures and properties. By introducing the phenylethynyl group into a coumarin dye as the sensing group, the ratiometric fluorescent probe CP was developed to selectively and rapidly discriminate between Cys and Hcy. With a single-wavelength excitation, the presence of Cys or Hcy induced the probe to produce distinct ratiometric fluorescence changes: from red (λmaxem = 608 nm) to blue (λmaxem = 485 nm) toward Cys and from red to mixed red/blue toward Hcy. Moreover, the probe was capable of visualizing and discriminating between intracellular Cys and Hcy in HeLa cells and zebrafish by exhibiting different ratiometric fluorescence signals.
Subject(s)
Cysteine , Fluorescent Dyes , Animals , Glutathione , HeLa Cells , Homocysteine , Humans , Spectrometry, Fluorescence , ZebrafishABSTRACT
Hypochlorous acid (HClO) is an important bactericide, and adjusting the content of HClO helps to improve the host's innate immunity and resist microbial invasion. Aggregation-induced luminescence (AIE) is the opposite of aggregation-induced quenching (ACQ). Compounds with AIE properties emit weakly in a dispersed state in solution and they can emit strong fluorescence in an aggregated state. In this article, we proposed a new AIE fluorescent probe QM-ClO based on the quinoline-malononitrile (QM) fluorophore and dimethylthiocarbamate (DMTC) to detect HClO. The probe QM-ClO showed a fast response time, a low detection limit of 30.8 nM and a large Stokes shift (190 nm). Carbonyl cyanide metachlorophenyl-hydrazone (CCCP) was used to induce cell apoptosis, and then an increase in the HClO content was observed in the cell. It is proved that cell apoptosis can lead to the increase of the HClO content in the cell. This probe provides an effective tool for studying apoptosis-related diseases.
Subject(s)
Fluorescent Dyes , Hypochlorous Acid , Apoptosis , Microscopy, Fluorescence , Optical ImagingABSTRACT
The elusive mechanism of action between signaling molecules H2O2 and H2S in oxidative stress demands a fluorescent probe, capable of their detection in a discriminative and dynamic manner. Herein we report the design and study of a probe TCAB. As demonstrated, it responds to H2O2 and H2S selectively and sensitively to generate distinct fluorescence signals and patterns. Cyan imaging for H2O2 in a ratiometric fashion and two-colored, enhanced blue and newly produced red for H2S are observed. When both are present, the sequential reaction of H2O2 and H2S with the probe gives cyan then red signal, while the reverse sequence produces an inverse red-cyan signal. The unrivaled discriminative multicolor imaging capacity of the probe enables us to monitor dynamic H2O2 and H2S redox processes in living cells and organisms. It is expected that the probe could serve as a powerful tool to investigate the correlation and distinction of biologically significant H2S- and H2O2-engaged redox processes.
Subject(s)
Fluorescent Dyes/chemistry , Hydrogen Peroxide/analysis , Hydrogen Sulfide/analysis , Animals , Fluorescent Dyes/chemical synthesis , HeLa Cells , Humans , Hydrogen Peroxide/metabolism , Hydrogen Sulfide/metabolism , Microscopy, Fluorescence , Molecular Structure , Optical Imaging , Oxidation-Reduction , Tumor Cells, Cultured , ZebrafishABSTRACT
As two important reactive oxygen species, hydrogen peroxide (H2O2) and hypochlorous acid (HClO) play vital roles in many physiological and pathological processes. However, the relationship between these two species is seldom investigated, in part, because of the lack of robust molecular tools that can simultaneously visualize HClO and H2O2 in biosystems. In this work, we present a design strategy to construct a single fluorescent probe that can detect H2O2 and HClO by simultaneously monitoring two distinct detection channels. In the design, one phenothiazine-based coumarin serves as a chromophore and sensor for HClO, while a second coumarin precursor containing a boronate ester acts as a sensor for H2O2. After a head-to-head screening of three candidates differing in their coumarin precursor moieties, probe CSU1 was found to have the optimal characteristics. As shown experimentally, it is able to detect them selectively and sensitively to generate distinct fluorescence signals and patterns in living cells. Furthermore, the endogenous generation of HClO from H2O2 and Cl- catalyzed by myeloperoxidase enzyme in living cells can be clearly monitored by the probe. These studies demonstrate the potential of the probe as a powerful tool to investigate the interplay of HClO and H2O2 in oxidative stress.
Subject(s)
Fluorescent Dyes/chemistry , Hydrogen Peroxide/analysis , Hypochlorous Acid/analysis , Cell Survival/drug effects , Fluorescent Dyes/pharmacology , Humans , Hydrogen Peroxide/metabolism , Hypochlorous Acid/metabolism , MCF-7 Cells , Molecular Structure , Optical Imaging , Peroxidase/metabolism , Tumor Cells, CulturedABSTRACT
By introducing the tetrahydroquinoxaline group as the electron donor to enhance intramolecular charge transfer effect, we deliberately designed a coumarin derivative, TQC-HClO, to serve as a two-photon ratiometric fluorescent probe for imaging hypochlorous acid in cells and zebra fish with good sensitivity and high selectivity. TQC-HClO displayed an obvious two-photon absorbance cross-section (over 100 GM in 800-840 nm), large Stokes shifts (159 to 173 nm), and a ratiometric fluorescence change from orange (λmaxem = 583 nm) to red (λmaxem = 650 nm) in response to hypochlorous acid.
ABSTRACT
Strong oxygen dependence, poor tumor targeting, and limited treatment depth have been considered as the "Achilles' heels" facing the clinical usage of photodynamic therapy (PDT). Different from common approaches, here, we propose an innovative tactic by using photon-initiated dyad cationic superoxide radical (O2-â¢) generator (ENBOS) featuring "0 + 1 > 1" amplification effect to simultaneously overcome these drawbacks. In particular, by taking advantage of the Förster resonance energy transfer theory, the energy donor successfully endows ENBOS with significantly enhanced NIR absorbance and photon utility, which in turn lead to ENBOS more easily activated and generating more O2-⢠in deep tissues, that thus dramatically intensifies the type I PDT against hypoxic deep tumors. Moreover, benefiting from the dyad cationic feature, ENBOS achieves superior "structure-inherent targeting" abilities with the signal-to-background ratio as high as 25.2 at 48 h post intravenous injection, offering opportunities for accurate imaging-guided tumor treatment. Meanwhile, the intratumoral accumulation and retention performance are also markedly improved (>120 h). On the basis of these unique merits, ENBOS selectively inhibits the deep-seated hypoxic tumor proliferation at a low light-dose irradiation. Therefore, this delicate design may open new horizons and cause a paradigm change for PDT in future cancer therapy.
Subject(s)
Photochemotherapy , Superoxides/metabolism , Animals , Cell Line, Tumor , Cell Transformation, Neoplastic , Intracellular Space/metabolism , Intracellular Space/radiation effects , Mice , Tumor Hypoxia/drug effects , Tumor Hypoxia/radiation effectsABSTRACT
Biothiols are essential reactive sulfur species (RSS), which play crucial roles in various critical physiological activities. To clarify their complex correlations in signal transduction and metabolism pathways, methods to distinguish H2S, cysteine (Cys), homocysteine (Hcy), and glutathione (GSH) at the same time are highly needed. Herein, we deliberately integrate 7-diethylcoumarin and resorufin through an ether bond to develop RC for simultaneous differentiation of Cys, Hcy, GSH, and H2S for the first time. RC displays distinct fluorescence colors in response to H2S, Cys, Hcy, and GSH as red, blue-red, blue-green-red, and green-red, respectively, both in aqueous media and living cells. This work not only reported a robust molecule, RC, to disentangle the intricate interplay networks among different biothiols in biosystems but also demonstrated a strategy for the design of multisignal fluorescent probes for the simultaneous sensing of diverse RSS species as well as other biological species.