Resonance Energy Transfer System Research Articles

A FeS2NPs-Luminol-MnO2NSs system based on chemiluminescence resonance energy transfer platform for sensing glutathione.

In this work, ferrous disulfide nanoparticles (FeS2NPs) with oxidase properties were synthesized, and a FeS2NPs-Luminol-MnO2 nanosheets (MnO2NSs) chemiluminescence resonance energy transfer (CRET) system was successfully established. Because of reaction with MnO2NSs, glutathione (GSH) can inhibit CRET between Luminol and MnO2NSs and recover the luminescence intensity of FeS2NPs-Luminol. Consequently, we developed a GSH sensor based on this chemiluminescence resonance energy transfer (CRET) system. Under optimal conditions, the FeS2NPs-Luminol-MnO2NSs sensing system showed very sensitive response to GSH in the range of 1μM-500 μM. The limit of detection of GSH reached as low as 0.15μM. Finally, the sensor was successfully used for the detection of GSH in serum.

FRET-based hACE2 receptor mimic peptide conjugated nanoprobe for simple detection of SARS-CoV-2

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection has led to a pandemic of acute respiratory disease, namely coronavirus disease (COVID-19). This disease threatens human health and public safety. Early diagnosis, isolation, and prevention are important to suppress the outbreak of COVID 19 given the lack of specific antiviral drugs to treat this disease and the emergence of various variants of the virus that cause breakthrough infections even after vaccine administration. Simple and prompt testing is paramount to preventing further spread of the virus. However, current testing methods, namely RT-PCR, is time-consuming. Binding of the SARS-CoV-2 spike (S) glycoprotein to human angiotensin-converting enzyme 2 (hACE2) receptor plays a pivotal role in host cell entry. In the present study, we developed a hACE2 mimic peptide beacon (COVID19-PEB) for simple detection of SARS-CoV-2 using a fluorescence resonance energy transfer system. COVID19-PEB exhibits minimal fluorescence in its ‘‘closed’’ hairpin structure; however, in the presence of SARS-CoV-2, the specific recognition of the S protein receptor-binding domain by COVID19-PEB causes the beacon to assume an ‘‘open’’ structure that emits strong fluorescence. COVID19-PEB can detect SARS-CoV-2 within 3 h or even 50 min and exhibits strong fluorescence even at low viral concentrations, with a detection limit of 4 × 103 plaque-forming unit/test. Furthermore, in SARS-CoV-2-infected patient samples confirmed using polymerase chain reaction, COVID19-PEB accurately detected the virus. COVID19-PEB could be developed as a rapid and accurate diagnostic tool for COVID-19.

Dual selective sensor for exosomes in serum using magnetic imprinted polymer isolation sandwiched with aptamer/graphene oxide based FRET fluorescent ignition

The selective and sensitive detection of cancerous exosomes in serum is critical for early disease diagnosis and improved prognosis. Previous exosome-related research has been limited by a lack of well-understanding in exosomes as well as the challenging background interference of body fluid. Molecularly imprinted polymers (MIPs) and nucleic acid aptamers can be regarded as the two alternatives to antibodies. When using imprinted polymer technology, comprehensive and precise information about the target constituents is not required. In this study, a novel kind of dual selective fluorescent nanosensor for the poorly characterized exosomes was constructed by integrating magnetic MIP selective exosome capture sandwiched with an aptamer/graphene oxide fluorescence resonance energy transfer system (FRET) based selective ‘turn-on’ exosome labeling heterogeneously. The overall strategy performance was successively evaluated using lysozyme and exosomes as targets. Good linearity and high sensitivity achieved were demonstrated. The LOD of exosomal detection in serum was 2.43 × 106 particles/mL, lower than other immunology based detection methods. The discrimination between serum from breast cancer patients and healthy people was also primarily studied. In conclusion, the developed sensor with outstanding selectivity, high detection sensitivity, simplicity, low cost, and wide applicability for known or unknown targets present significant potential in challenging clinical diagnosis.

Turn –on FRET-based cysteine sensor by sulfur-doped carbon dots and Au nanoparticles decorated WS2 nanosheet

Cysteine is an essential biothiol that plays various functions in the human body. Decrease or exceeding of this excellent antioxidant from the expected range will lead to so many problems. Thus, appropriate sensing of it would be of great importance. Sulfur-doped carbon Dots(S-CDs) owe excellent fluorescence emission. Therefore, designing a Fluorescence resonance energy transfer (FRET) system between S-CDs as donor and Au nanoparticles (AuNPs) decorated tungsten disulfide nanosheet (WS2 NSs) would be a perfect strategy for cysteine detection. Excitation at 340 nm will give the maximum quantum yield of S-CDs (21%) and fluorescence emission peak at 460 nm. In the presence of cysteine, the FRET mechanism inhibited through the affinity of cysteine's functional groups (-SH and -NH2) toward AuNPs and S-CDs fluorescence emission was recovered. To find the best efficiency of the system, optimization of pH, temperature, and time was investigated. Here the linear range of 3–275 µM and limit of detection of 0.01 µM was obtained. Finally, the fluorescence method was applied to the analysis of cysteine in human blood serum, which poses the potential of rapid and sensitive sensing. It can detect both lower and higher amounts of serum cysteine.

Electrochemiluminescence Resonance Energy Transfer System Based on Silver Metal-Organic Frameworks as a Double-Amplified Emitter for Sensitive Detection of miRNA-107.

As a class of electrochemiluminescence (ECL) enhancers, silver-based materials have broad application prospects. In this work, a novel silver metal-organic framework (AgMOF) was developed as a self-enhanced ECL emitter by one-step mixing and standing at room temperature. The AgMOF could produce strong and stable ECL emissions based on a double-amplification method, which originated from the aggregation-induced ECL emission of ligands and catalyzing S2O82- to produce more SO4•- by silver. Moreover, an ECL resonance energy transfer (ECL-RET) biosensor with AgMOF as a donor and BHQ2 as an acceptor was fabricated by duplex-specific nuclease (DSN)-assisted target recycling amplification to detect miRNA-107. The biosensor exhibited a strong ECL-RET effect due to the higher ECL emission of the AgMOF and perfect match of spectra between the AgMOF and BHQ2. Upon the introduction of DSN and target miRNAs, the specific DNA-RNA binding and nuclease cleaving could trigger the detachment of BHQ2, resulting in an increased ECL signal of AgMOF. Benefiting from the ECL-RET and DSN-assisted target recycling amplification methods, this biosensor achieved a wide linear relationship range from 20 to 120 fM with a low limit of detection (4.33 fM). This research presents an effective emitter for self-enhanced ECL systems, which broadens the potential ECL applications of silver-based nanomaterials.

A ratiometric fluorescent probe based on peptide modified MnFe2O4 nanoparticles for matrix metalloproteinase-7 activity detection in vitro and in vivo.

Abnormal expression of matrix metalloproteinases plays an important role in tumor invasion and metastasis. In this report, a peptide modified MnFe2O4 ratiometric fluorescent nanoprobe is developed for noninvasively visualizing the distribution of matrix metalloproteinase-7 (MMP-7) in vitro and in vivo. A fluorescein isothiocyanate (FITC) modified peptide containing the specific motif VPLSLTMG for MMP-7 cleavage was conjugated with MnFe2O4 nanoparticles (NPs) to establish a Förster resonance energy transfer (FRET) system for sensing the protease. The rhodamine B (RhB) modified targeting peptide immobilized on the nanoparticle surface was not only used as an internal reference for forming a ratiometric fluorescence system together with the FITC dye, but also used for enhancing the tumor targeting ability. The tumor accumulation amount of the as-developed ratiometric fluorescent probe (termed MnFe2O4-pep-dyes) can be measured by T2-weighted magnetic resonance (T2-weighted MR) imaging because MnFe2O4 NPs display an excellent T2-weighted MR contrast ability. In the presence of MMP-7, FITC detached from the MnFe2O4 surface resulting in the recovery of FITC fluorescence, while no obvious change of the RhB fluorescence was observed. The recovery ratio of FITC to RhB fluorescence intensity is linearly dependent on the MMP-7 concentration within the range of 0.1 to 15 nM in buffer and 5 × 102 to 1 × 104 cells in cell lysates with a limit of detection of 0.1 nM and 436 cells, respectively. MnFe2O4-pep-dyes was further applied to spatially observe MMP-7 expression in a tumor-bearing mouse by in vivo fluorescence imaging with external magnetic field assistance for demonstrating its practicability.

Nonradiative Energy Transfer from CsPbBr3 Nanocrystals to CdSe/CdS Nanocrystals for Efficient Light Down Conversion.

Semiconductor nanocrystals (NCs) are emerging luminescent materials with superior optical properties. However, the light-conversion application of NCs is restricted by reabsorption-induced fluorescent quenching. Here, a NC-NC Förster resonance energy transfer (FRET) system is developed by employing large CsPbBr3 NCs as donors and CdSe/CdS NCs as acceptors. The FRET systems using toluene and octadecene as solvents show decreases of 10% and 14%, respectively, in the integrated photoluminescence (PL) intensity, far below the reabsorption loss observed in concentrated CdSe/CdS NCs (>30%) at the same color purity. Notably, we demonstrate by transient absorption measurements that the styrene-mediated FRET system involves a Dexter energy transfer process, which enables the harvesting of triplet excitons and leads to an additional PL enhancement at system level by a maximum of 40% instead of fluorescence quenching. The remarkably improved light-conversion efficiency and antiquenching property make the proposed NC-NC system superior in light down-conversion applications.

Chemiluminescence resonance energy transfer determination of uric acid with fluorescent covalent organic framework as energy acceptor

A simple and feasible strategy was developed for the preparation of fluorescent covalent organic frameworks (COFs) TpPa-1@FL. The TpPa-1–1@FL was prepared via a self-assembly strategy by soaking non-fluorescent COFs TpPa-1 into strong fluorescent fluorescein (FL) solution. A chemiluminescence resonance energy transfer (CRET) system was constructed by the combination strong fluorescent TpPa-1@FL with TCPO-hydrogen peroxide (H2O2) reaction. The chemiluminescence (CL) signal of the system was further improved by the addition of bovine serum albumin (BSA). The CRET system can determine H2O2 with a linear range response from 5.0 µmol/L to 20.0 mmol/L and a detection limit of 1.1 µmol/L. The CRET system was further exploited for indirect detection of uric acid with coupling of uricase. A good linear relationship was obtained for uric acid in the 10.0–400.0 µmol/L concentration range with a detection limit of 3.8 µmol/L. The practicability of this method was assessed by the determination of uric acid in real samples of human serum and urine.

Regenerative Flexible Upconversion-Luminescence Biosensor for Visual Detection of Diethylstilbestrol Based on Smartphone Imaging.

Diethylstilbestrol (DES), an endocrine disrupting chemical, has been linked to serious health problems in humans. In this work, a regenerative flexible upconversion-fluorescence biosensor was designed for the detection of DES in foodstuffs and environmental samples. Herein, amino-functionalized upconversion nanoparticles (UCNPs) were synthesized and immobilized on the surface of a flexible polydimethylsiloxane substrate, which was further modified with complementary DNA and dabcyl-labeled DES aptamer. The fluorescence resonance energy transfer (FRET) system was established for DES detection between dabcyl and UCNPs as the acceptor and donor pairs, respectively, which resulted in the quenching of the upconversion luminescence intensity. In the presence of a target, the FRET system was destroyed and upconversion fluorescence was restored due to the stronger affinity of the aptamer toward DES. The designed biosensor was also implemented in a dual-mode signal readout based on images from a smartphone and spectra from a spectrometer. Under the optimized experimental conditions, good linear relationships were achieved based on imaging (y = 53.055x + 36.175, R2 = 0.9851) and spectral data (y = 1.1582x + 1.9561, R2 = 0.9897). The designed biosensor revealed great practicability with a spiked recovery rate of 77.91-97.95% for DES detection in real environment and foodstuff samples. Furthermore, the proposed biosensor was regenerated seven times with an accuracy threshold of 80% demonstrating its durability and reusability. Thus, this biosensor is expected to be applied to point-of-care and on-site detection based on the developed portable smartphone device and android application.

Preparation and application of multi-wavelength-regulated multi-state photoswitchable fluorescent polymer nanoparticles

The photoswitchable system with color and multi-state fluorescence changes is the key to the realization of advanced multi-level information storage, and its application potential has far exceeded the monochromatic fluorescent system. Herein, we introduced a novel multi-state photoswitchable fluorescent polymeric nanoparticles, which contains two energy-matched photoswitchable fluorescent molecules, i.e. diarylethene derivative (BH, donor) and spiropyran derivative (SPMA, acceptor), to construct a tunable fluorescence resonance energy transfer (FRET) system. By optimizing the feeding ratio of the two photochromic molecules to control the efficiency of energy transfer, the fluorescence of the nanoparticles can be reversibly switched among none, red, orange, and green by adjusting the wavelength of light stimuli. In addition, the nanoparticles display good water dispersibility, high brightness, fast responsiveness, excellent photoreversibility, and long-term fluorescence stability. We also verified that the system has great potential in optical data storage, multi-layer information encryption, and anti-counterfeiting.

An improved macromolecular crowding sensor CRONOS for detection of crowding changes in membrane-less organelles under stressed conditions

Membrane-less organelles (MLOs) formed by liquid-liquid phase separation (LLPS) play pivotal roles in biological processes. During LLPS, proteins and nucleotides are extremely condensed, resulting in changes in their conformation and biological functions. Disturbed LLPS homeostasis in MLOs is thought to associate with fatal diseases such as amyotrophic lateral sclerosis. Therefore, it is important to detect changes in the degree of crowding in MLOs. However, it has not been investigated well due to the lack of an appropriate method. To address this, we developed a genetically encoded macromolecular crowding sensor CRONOS (crowding sensor with mNeonGreen and mScarlet-I) that senses the degree of macromolecular crowding in MLOs using a fluorescence resonance energy transfer (FRET) system. CRONOS is a bright biosensor with a wide dynamic range and successfully detects changes in the macromolecular volume fraction in solution. By fusing to the scaffold protein of each MLO, we delivered CRONOS to MLO of interest and detected previously undescribed differences in the degree of crowding in each MLO. CRONOS also detected changes in the degree of macromolecular crowding in nucleolus induced by environmental stress or inhibition of transcription. These findings suggest that CRONOS can be a useful tool for the determination of molecular crowding and detection of pathological changes in MLOs in live cells.

Highly selective and sensitive detection of glutathione over cysteine and homocysteine with a turn-on fluorescent biosensor based on cysteamine-stabilized CdTe quantum dots

In this work, cysteamine (CA) stabilized CdTe quantum dots (QDs) (CA-CdTe QDs) and sodium citrate stabilized gold nanoparticles (AuNPs) were prepared. Because of the strong electrostatic interaction and spectral overlap of emission spectrum of CA-CdTe QDs and absorption spectrum of AuNPs, a highly effective fluorescence resonance energy transfer (FRET) system was formed and the fluorescence of CA-CdTe QDs was strongly quenched. The synthesized CA-CdTe and AuNPs were self-assembled to large clusters due to the electrostatic attraction and the fluorescence of CA-CdTe was sharply quenched as a result of FRET. Under the optimum pH of 5.5, the positive GSH could assemble with negative AuNPs through electrostatic interaction and destroy the FRET system of CA-CdTe and AuNPs, due to the red shift of absorption wavelength of AuNPs caused by aggregation. The fluorescence of CA-CdTe recovered, and the recovered fluorescence efficiency shows a linear function against the GSH concentrations from 6.7 nM to 0.40 μM, with a detecting limit of 3.3 nM. The quenched emission of CA-CdTe could be recovered attributed to the aggregation of AuNPs by GSH. Under optimal conditions, the sensing system was successfully applied in the detection of GSH in real human blood plasma samples with a recovery of 99.5–102.3%, showing a promising future for the highly sensitive and selective GSH detection in the human blood plasma samples.

Highly stable fluorescent probe based on mesoporous silica coated quantum dots for sensitive and selective detection of Cd2+

Cadmium ions have been of crucial concern due to the high biological toxicity and serious environmental risks. Various fluorescent Cd-sensitive probes have been reported with improved sensing properties, but still severely suffer from poor stability and insufficient selectivity. In this work, a stable fluorescent probe based on silica encapsulated quantum dots (QDs) have been developed for rapid, sensitive and selective detection of cadmium ion. To improve fluorescence stability, the strategy of mesoporous silica encapsulation was adopted, in which the mesoporous silica shell offers numerous channels for Cd2+. Further, the Forster Resonance Energy Transfer (FRET) system, where QDs@mSiO2 and rhodamine B (RB) are used as donors and acceptors respectively, has been constructed, in which the mesoporous silica shell also serves as spacers with tunable thickness for controlling the QD-RB distance. Under optimal conditions, the probes possess a sensitive fluorescence response with a detection limit of 1.25 μM. Visual detection can be realized by the obvious fluorescence changes of the FRET system. In addition, the FRET system shows promising sensing performances both in tap water samples and rice-washed water samples, confirming a great potential for practical application.

Contrary Logic Pair Library, Parity Generator/Checker and Various Concatenated Logic Circuits Engineered by a Label-Free and Immobilization-Free Electrochemiluminescence Resonance Energy Transfer System.

Herein, a label-free and immobilization-free electrochemiluminescence resonance energy transfer (ECL-RET) system based on graphitic carbon nitride nanosheets (GCNNs)/Ru(phen)32+ donor/acceptor pair is developed, in which the ECL-RET is regulated by regulating the diffusivity of Ru(phen)32+ molecules toward the negatively charged GCNNs through logically programmed DNA hybridization reactions. The two optical signals of GCNNs (445nm) and Ru(phen)32+ (593nm) show completely opposite changes through the same one-time DNA hybridization reaction. Based on this ECL-RET system, a contrary logic pair (CLP) library, a parity generator/checker system for differentiating the erroneous bits during data transmission, the parity checker to identify the even/odd natural numbers from 0 to 9, and a series of concatenated logic circuits including a six-input logic gate capable of implementing of 64 input combinations for meeting the needs of computational complexity are developed. The ECL-RET-based molecular logic system avoids the time-consuming, costly and inefficient labeling procedures and the laborious processes of immobilization, presenting great potential for building more complicated and advanced logic gates, and providing a refreshing inspiration for the construction of combinatorial logic circuits based on ECL method.

Mechanistic insight into human androgen receptor-mediated endocrine-disrupting potentials by a stable bioluminescence resonance energy transfer-based dimerization assay

To develop a novel cell-based assay to evaluate the androgenic endocrine-disrupting properties of chemical substances, we established a method to detect ligand-mediated androgen receptor (AR) dimerization in stably transfected human cell lines using a bioluminescence resonance energy transfer (BRET) system. Using stably transfected human embryonic kidney (HEK-293) cells, the BRET-based AR dimerization assay was optimized as a novel test method and was validated using test chemicals recommended by the Interagency Coordinating Committee on the Validation of Alternative Methods (ICCVAM). The BRET-based AR dimerization assay showed high accuracy, sensitivity, and specificity for the detection of androgenic endocrine-disrupting chemicals (EDCs), and the assay protocol is adequate for practical use. This dimerization assay is based on ligand-mediated hormone receptor dimerization and can provide accurate information about androgenic endocrine-disrupting properties at the cellular level, complementing conventional binding and transactivation assays.

Label-free triplex DNA-based biosensing of transcription factor using fluorescence resonance energy transfer between N-doped carbon dot and gold nanoparticle

Herein, a new turn-on fluorescent assay was established as a platform for the sensing of transcription factor NF-kB p50 based on triplex DNA labeled with N-doped carbon dots (NCDs) and gold nanoparticles (AuNPs) as donors and acceptors, respectively in the fluorescence resonance energy transfer (FRET) system. The synthetized nanoparticles were studied by different characterization techniques. A labeled DNA molecule was designed to form a triplex when no target protein existence and reported its formation by the change in FRET efficiency. While the triplex DNA was formed, the fluorescence of carbon dots at 503 nm (excitation at 460 nm) was quenched by FRET between NCD and AuNP. However, presence of NF-kB p50 followed by the considerable enhancement in the fluorescence intensity caused by the release of AuNPs labeled single stranded DNA from the triplex DNA structure, used for sensitive determination of the transcription factor. This technique showed a linearity (R2 = 0.9943) in the range of 20–150 pM with a limit of detection of 9 pM for the determination of NF-kB p50. Moreover, the sequence-specific triplex-based biosensor could discriminate NF-kB p50 from the other proteins with high selectively. Our results suggest that the biosensor provides a generalizable platform for rapid detection of NF-kB p50 in synthetic medium, promising in prevention and early diagnosis of cancer.

Quantitative Förster Resonance Energy Transfer: Efficient Light Harvesting for Sequential Photo-Thermo-Electric Conversion.

Light is essential to all life on the earth. Thus, highly efficient light-harvesting systems with the sequential energy transfer process are significant for using solar energy in photosynthesis. For developing an efficient light-harvesting system, a liquid aggregation-induced emission (AIE) dye TPE-EA is obtained, as a donor and solvent, which can light up the aggregation caused quenching (ACQ) Nile Red (NiR, acceptor) to construct a quantitative Förster resonance energy transfer (FRET) system in NiR⊂TPE-EA. Impressively, this FRET pair shows an impressive photothermal effect, producing a peak temperature of 119°C while excited by UV light, with 37.8% of conversion efficiency. NiR⊂TPE-EA is quite different from most other photothermal materials, which require excitation with long wavelength light (>520nm). Therefore, NiR⊂TPE-EA firstly converts the solar into thermal energy and then into electric energy to achieve sequential photo-thermo-electric conversion. Such sequential conversion, suitable for being excited by sunlight, is anticipated to unlock new and smart approaches for capturing solar energy.

Dual-quenching electrochemiluminescence resonance energy transfer system from IRMOF-3 coreaction accelerator enriched nitrogen-doped GQDs to ZnO@Au for sensitive detection of procalcitonin

Herein a novel electrochemiluminescence resonance energy transfer (ECL-RET) pair of isoreticular metal organic framework-3 (IRMOF-3) enriched nitrogen-doped graphene quantum dots (N-GQDs) luminescent material (N-GQDs@IRMOF-3@N-GQDs, donor) and Au nanoparticles modified zinc oxide nanorod (ZnO@Au, acceptor) were firstly designed to fabricate a dual-quenching sandwich-type ECL immunosensor for ultrasensitive analysis of procalcitonin (PCT). IRMOF-3 not only acted as a carrier for abundantly enriching luminescent N-GQDs by internal encapsulation and external decoration, but also a coreaction accelerator which could boost the transformation of persulfate ion S2O82− to generate more anion radical SO4−, so as to promote the ECL emission of N-GQDs. Additionally, Au nanoparticles were loaded onto the ZnO nanorods through in-situ modification to obtain ZnO@Au, which was firstly applied as a dual-quencher of ECL signal. In the best test environment, a wide detection range from 0.0001 to 100 ng mL−1 was obtained and the limit of detection is 12.58 fg mL−1 (S/N = 3). With excellent reproducibility and sensitivity, the practical test consequence of PCT in human serum samples was satisfactory. These results suggested that this sensing system could provide a reference model for effective detection of disease markers in clinical medicine.

AIEgens-based fluorescent covalent organic framework in construction of chemiluminescence resonance energy transfer system for serum uric acid detection.

A covalent organic framework (COF) with aggregation-induced emission (AIE) property was successfully synthesized through in situ marriage of a commonly used AIE molecule tetraphenylethylene (TPE) with Schiff base network (SNW-1) through a simple one-pot method. The TPE@SNW-1 was characterized with different techniques of Fourier transform infrared spectroscopy, X-ray diffraction, transmission electron microscopy, scanning electron microscopy, and nitrogen adsorption/desorption experiments. The fluorescence of the TPE@SNW-1 strongly depends on the composition of tetrahydrofuran-water binary system. The AIE property of TPE@SNW-1 was directly supported with particle size distribution by dynamic light scattering technique. With the TPE@SNW-1 as an energy acceptor, a chemiluminescence resonance energy transfer (CRET) system was constructed with bis(2,4,6-trichlorophenyl) oxalate (TCPO)-hydrogen peroxide (H2O2) reaction as an energy donor. The chemiluminescence (CL) signal displays a good linear relationship with concentration of H2O2 in the 5.0-1000.0 μmol·L-1 range, and a detection limit of 2.34 μmol L-1. The system was further exploited to determine uric acid based on the fact that equal stoichiometric amount of H2O2 can be concurrently generated under the catalysis of uricase. The procedure exhibits a linear response to uric acid concentration in the range 10.0-150.0 μmol·L-1 and a detection limit of 4.94 μmol·L-1. The practicability of the method was demonstrated in the determination of uric acid in human serum samples.

MnO2 Nanospheres Assisted by Cysteine Combined with MnO2 Nanosheets as a Fluorescence Resonance Energy Transfer System for "Switch-on" Detection of Glutathione.

Manganese dioxide nanosheets combined with cysteine-assisted emitting manganese dioxide nanospheres (Cys-MnO2 nanospheres) is fabricated for the first time as an "off-on" fluorescence detection platform for glutathione (GSH). In this sensing system, Cys-MnO2 nanospheres served as energy donors, while MnO2 nanosheets were used as both energy acceptors and recognition units. MnO2 nanosheets can effectively quench the fluorescence of Cys-MnO2 nanospheres through the fluorescence resonance energy transfer (FRET). The addition of GSH could reduce MnO2 nanosheets into Mn2+, disrupting the FRET process and restoring the fluorescence of Cys-MnO2 nanospheres. Under the optimum conditions, the "switch-on" platform we established has a wide response to GSH with a range of 5-50 μM and 150-800 μM, as well as a superior specificity. Importantly, all components of the sensor are nontoxic, biocompatible, easily prepared, and have a high utilization of raw materials. Moreover, the sensing system achieved satisfactory results in human serum, showing a tremendous potential in the field of biomedicine.