key: cord-0023460-dzddy7ti
authors: Yeom, Gyu Seong; Song, In-ho; Warkad, Shrikant Dashrath; Shinde, Pramod B.; Kim, Taewoon; Park, Seong-min; Nimse, Satish Balasaheb
title: Development of a Novel Benzimidazole-Based Probe and Portable Fluorimeter for the Detection of Cysteine in Human Urine
date: 2021-10-26
journal: Biosensors (Basel)
DOI: 10.3390/bios11110420
sha: 2df5c3099d8e5b959e440dded4c64068a81f5dd2
doc_id: 23460
cord_uid: dzddy7ti

The measurement of cysteine in human urine and live cells is crucial for evaluating biological metabolism, monitoring and maintaining the immune system, preventing tissue/DNA damage caused by free radicals, preventing autoimmune diseases, and diagnosing disorders such as cystinuria and cancer. A method that uses a fluorescence turn-on probe and a portable fluorescence spectrometer device are crucial for highly sensitive, simple, rapid, and inexpensive cysteine detection. Herein, we present the synthesis and application of a benzimidazole-based fluorescent probe (ABIA) along with the design and development of a portable fluorescence spectrometer device (CysDDev) for detecting cysteine in simulated human urine. ABIA showed excellent selectivity and sensitivity in detecting cysteine over homocysteine, glutathione, and other amino acids with the response time of 1 min and demonstrated a detection limit of 16.3 nM using the developed CysDDev. Further, ABIA also demonstrated its utility in detecting intracellular cysteine, making it an excellent probe for bio-imaging assay.

Biothiols such as cysteine (Cys), homocysteine (Hcy), and glutathione (GSH) play a vital role in numerous biological reactions [1] [2] [3] [4] [5] [6] . It is important to note that among other biothiols, Cys deficiency exhibits several disorders, including edema, liver damage, muscle and fat loss, narcolepsy, skin damage, and weakness [7] [8] [9] . On the other hand, elevated cysteine levels are often correlated with cystinuria, a metabolic disorder characterized by the urinary loss of amino acids including Cys, arginine, ornithine, and lysine [10] . Therefore, measuring Cys in human urine and live cells is crucial for evaluating biological metabolism, monitoring and maintaining the immune system, preventing tissue/DNA damage caused by free radicals, preventing autoimmune diseases, and diagnosing disorders such as cystinuria and cancer.

There have been tremendous advances in developing methods for detecting biothiols in serum and live cells [11] [12] [13] [14] . The development of fluorescent probes for detecting Cys has attracted significant attention from the broader scientific community [15] [16] [17] [18] . The simplicity, high sensitivity and selectivity, and suitability for noninvasive and real-time detection are the significant advantages of methods based on fluorescent probes [19] [20] [21] [22] . Though there are numerous reports on mechanistically different fluorescent probes for Biosensors 2021, 11, 420 2 of 15 detecting biothiols [23] [24] [25] [26] , only a few have been applied to simultaneously detect Cys in human urine and live-cell imaging [27] [28] [29] . Therefore, using a fluorescent probe that can detect Cys in human urine and live cells can result in an excellent method for diagnosing cystinuria and Cys-related disorders [30] .

There have been several reports on the colorimetric detection of Cys using paperbased devices [31, 32] . However, proteins and large quantities of amino acids can interfere in color development reactions. The other disadvantage of paper-based devices is a higher limit of detection (LOD) [33, 34] . Hence, paper-based devices can only provide qualitative information on urinary cysteine. Further, the fluorescence-based detection of Cys in biological fluids is advantageous over other methods due to its simple operating procedure, high sensitivity and selectivity for Cys in the presence of other proteins and amino acids, lower LOD, and the possibility of developing a portable device applicable in point-of-care settings.

Herein, we report on developing and applying a Cys specific fluorescent probe and the portable device for detecting cysteine in urine. The probe ABIA (2-(anthracen-9-yl)-5methyl-1H-benzo[d]imidazole-acrylamide), an organic dye, was prepared in a two-step reaction and was evaluated as the target probe for biothiols. ABIA demonstrated excellent selectivity for Cys over other biothiols and amino acids, with a response time of a mere 1 min. The application of ABIA in live-cell imaging was evaluated by inverted fluorescence microscopy in a lung cancer cell line (A549), proving that ABIA as a suitable tool for tracking Cys in vitro. Its applicability in detecting Cys in live cells and simulated urine prompted us to develop a portable fluorimeter. The design and development of Cys detection device (CYsDDev) is also elaborated upon here. ABIA and CysDDev allow the detection of Cys in simulated urine, with a LOD of 16.3 nM.

Reagents and required chemicals were procured either from Sigma-Aldrich (Seoul, Korea) or TCI (Seoul, Korea) and were used as received unless stated otherwise. The simulated urine (product code, 84 0679) was obtained from Biozoa Biological Supply Company (Seoul, Korea). The reactions were conducted under an inert atmosphere (argon gas). Completion of the reaction was monitored using thin-layer chromatography (TLC) by visualizing the plates under UV light (254 nm). DMSO-d6 was used as a solvent to characterize synthesized compounds by 1 H-and 13 C-NMR spectroscopy on a Jeol FT-NMR spectrometer (400 MHz; JEOL, Tokyo, Japan). The chemical shifts (δ) and the coupling constants (J) were reported as ppm and Hz, respectively. The Shimadzu UV-24500 (Shimadzu, Tokyo, Japan) spectrometer and Agilent Cary Eclipse fluorescence spectrophotometer (Agilent Technologies, Santa Clara, CA, USA) were used to record UV-visible spectra and fluorescence emission spectra, respectively. A JMS-700 MStation Mass Spectrometer (JEOL, Tokyo, Japan), a microplate Reader Spectramax Plus 384 (Molecular Devices, San Jose, CA, USA), and a confocal laser scanning microscope (Carl Zeiss LSM710, Osnabrück, Germany) were also used in the present study. The material for 3D printing and the electronic components required for the development of CysDDev were procured from Devicemart (Seoul, Korea) and Mouser Electronics (Seoul, Korea). A CUBICON Single Plus 320C (Jungwon, Korea) 3D printer was used to fabricate various parts and the body of CysDDev.

A solution of anthracene-9-carbaldehyde (0.84 g, 4.07 mmol) in ethanol (10 mL) was slowly added dropwise to a solution of 4-methylbenzene-1,2-diamine (0.5 g, 4.09 mmol) in ethanol (20 mL) with a dropping funnel for 2 h. Then, the reaction mixture was continually stirred under air at room temperature until the completion of the reaction. The progress of the reaction was monitored by TLC using an ethyl acetate:hexanes (3:7) mixture. The precipitated product was filtered. The filter cake was washed with three aliquots of 10 mL ethanol followed by vacuum drying to obtain the final product: beige-colored powder. Yield: 1.01 g (80%). 1 

A solution of compound 3 (0.1 g, 0.32 mmol), triethylamine (0.18 mL, 1.29 mmol), and DMAP (0.004 g, 0.033 mmol) in anhydrous tetrahydrofuran (25 mL) was stirred at 0 • C under argon gas for 30 min. Then, prop-2-enoyl chloride (0.104 mL, 1.29 mmol) was slowly added to the reaction mixture and continued to be stirred until the completion of the reaction. The reaction progress was monitored by TLC using an ethyl acetate:hexanes (3:7) mixture. After the completion of the reaction (1 h), 100 mL of CH 2 Cl 2 was added to the reaction mixture. Then, the reaction mixture was washed three times with the 150 mL aliquots of saturated Na 2 CO 3 followed by a single wash of 150 mL brine. The separated organic layer was then dried over anhydrous MgSO 4 , and the solvent was evaporated under reduced pressure to obtain the crude product, which was then purified by column chromatography (SiO 2 , ethyl acetate/hexane = 1/20, v/v). The final compound was obtained as a light yellow solid. Yield 82 mg (74%). 1 Figure S7 and Table S1 ). HR-EIMS + : m/z = 362.1418 (M) + (Calcd for C 25 H 18 N 2 O, 362.14).

The double-distilled water and spectroscopic grade DMSO were used to prepare the stock and working solutions. The working solution of ABIA (10 For sensitivity study, the titration experiments were accomplished through a stepwise addition of 1.15 equivalents of Cys (1 mM) to a solution of ABIA (10 µM). The absorbance intensity and emission intensity were recorded in the range of 200-600 nm and 350-650 nm, respectively, alongside a reagent blank. The effect of reaction time on the Cys detection was determined by tracing the fluorescence intensity of ABIA (10 µM) in the presence of five equivalent Cys (50 µM) for 0 to 60 min. The response of ABIA for reaction with Cys obeyed pseudo-first-order kinetics. Therefore, the rate constant was calculated according to the following equation (Equation (1)) [35] : (1) where F is the fluorescence intensity at time t, F max is the fluorescence intensity after the reaction, and k is the rate constant. The fluorescence intensity was recorded at λ ex /λ em = 368/470 nm alongside a reagent blank with the excitation and emission slits set to 5.0 nm.

The 3D models of various parts and the main case were created in Autodesk Fusion 360 software. The device's overall size was 130 × 120 × 50 mm (W × D × H). CysDDev was assembled with several parts, including the cuvette holder, mounting holes for the LED and sensor, lid for the LED and sensor, the main case, and a top cap lid for the cuvette holder. The cuvette holder could hold a plastic or quartz cuvette with the dimensions of 12.5 × 12.5 × 45 mm dimension. The main body had a hole connecting the device to the computer. When completely assembled and when the top cap lid was mounted, there was no significant light entering the measuring device. Apart from the top cap lid for the cuvette holder, there were no moving components in the device, making it easy to fabricate and assemble. The CysDDev prototype was optimized for fused deposition modeling (FDM) 3D printing. All three parts of the design were printed separately with black thermoplastic filament to lower the reflectivity of the internal surfaces. The electronics parts of the CYSDDev consisted of 9 V battery, a sensor (Hamamatsu micro-spectrometer C12666MA, Japan) with the detection range λ = 340-850 nm), a UV LED (15 mA, λ = 370 nm), an Arduino Uno R3 microcontroller for device control and data processing, and a computer connector cable. The LED drew power from a 9 V battery, and the Arduino microcontroller received the energy from the connected computer. The measured fluorescence profile of a sample by CysDDev was automatically converted into a Microsoft Excel file (.csv) consisting of the information on the wavelength (nm) and respective fluorescence intensity (a.u.).

The effect of pH (pH = 3-10) on the Cys detection using ABIA was examined by fluorescence spectroscopy. The tetrabutylammonium hydroxide and perchloric acid were used to adjust the pH of simulated human urine.

Usually, urine pH is slightly acidic, with typical values of 6.0 to 7.5. However, the range of urine pH is 4.5 to 8.0. Cys detection using ABIA and CysDDev was performed using simulated urine with a pH of 6.5. A standard curve was obtained by diluting a stock solution of Cys in analyte-free simulated human urine (0-150 µM). Each sample was serially diluted with the analyte-free urine to obtain solutions with concentrations in the detection range. The mean of ten fluorescence signal measurement values (SD in the range of 1.5-9.8%) for each calibration point was used to construct the standard curve. The LOD was estimated by applying the IUPAC recommended equation, LOD = 3σ/slope [36] . Where σ is the standard deviation of (n = 10) blank samples and the slope for the calibration curves.

A real urine sample obtained from a healthy volunteer was used for the spiking test and to validate the applicability of the ABIA and CysDDev in clinical samples. An amount of 5 µL urine from a healthy volunteer spiked with various Cys concentrations was added to the ABIA solution, and the fluorescence intensities were measured. Then, the percent recovery was measured using the standard curve.

The cytotoxicity assay (MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay) of ABIA, Cys, and Cys combined with the probe ABIA was performed using A549 cells (adenocarcinomic human alveolar basal epithelial cells), as reported earlier [37, 38] . In brief, about 7000 A549 cells per well were seeded in 96-well plates and were allowed to incubate for 24 h. Then, the solution in the wells was replaced by media containing ABIA, Cys, and ABIA with Cys (1, 10, 25, and 50 µM) and was incubated for another 24 h. The dimethyl sulfoxide (DMSO) was used as a control. About 200 µL of a media containing MTT solution was added to each well and was allowed to incubate for four hours at 37 • C. Finally, the absorbance was recorded at 570 nm to determine the cell cytotoxicity. The experiment was repeated three times, and the results were presented with mean and standard deviation.

The bio-imaging experiments were performed by seeding the A549 cells on glassbottom culture dishes and incubating them for 48 h. For control experiments, cells were only treated with the culture medium and were observed under the confocal microscope after being washed three times with 0.1 M PBS (0.5 mL). For treatment, cells were treated with 500 µM of Cys and 25 µM of ABIA separately and were allowed to incubate for 1 h at 37 • C and 5% CO 2 and were then washed three times with 0.1 M PBS (0.5 mL) before observation. For the bio-imaging of Cys by ABIA, cells were incubated with 500 µM of Cys for 1 h followed by replacing the media containing 25 µM of ABIA and incubating the cells for another 1 h. Then, the cells were washed three times with 0.1 M PBS (0.5 mL) before observation. For another control experiment, cells were treated with 1 mM N-ethylmaleimide (NEM, a biothiol scavenger) for 30 min at 37 • C followed by washing three times with 0.1 M PBS (0.5 mL). Then, the cells were incubated in the presence of 25 µM of ABIA for 1 h followed being washed three times with 0.1 M PBS (0.5 mL) before observation. In a similar experiment, cells pre-tread with NEM (1 mM), as mentioned above, were treated with Cys (500 µM, for 1 h) followed being washed with 0.1 M PBS (0.5 mL × 3) and then incubated in the presence of ABIA (25 µM, 1 h) and finally being washed three times 0.1 M PBS (0.5 mL) before observation. Finally, the PBS (1 mL) was added to each glass-bottom culture dish, and then the fluorescence images were recorded using a confocal microscope (Carl Zeiss LSM710).

The probe ABIA was synthesized in a two-step reaction as depicted in Scheme 1.

The cytotoxicity assay (MTT (3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide) assay) of ABIA, Cys, and Cys combined with the probe ABIA was performed using A549 cells (adenocarcinomic human alveolar basal epithelial cells), as reported earlier [37, 38] . In brief, about 7000 A549 cells per well were seeded in 96-well plates and were allowed to incubate for 24 h. Then, the solution in the wells was replaced by media containing ABIA, Cys, and ABIA with Cys (1, 10, 25, and 50 µM) and was incubated for another 24 h. The dimethyl sulfoxide (DMSO) was used as a control. About 200 µL of a media containing MTT solution was added to each well and was allowed to incubate for four hours at 37 °C. Finally, the absorbance was recorded at 570 nm to determine the cell cytotoxicity. The experiment was repeated three times, and the results were presented with mean and standard deviation.

The bio-imaging experiments were performed by seeding the A549 cells on glassbottom culture dishes and incubating them for 48 h. For control experiments, cells were only treated with the culture medium and were observed under the confocal microscope after being washed three times with 0.1 M PBS (0.5 mL). For treatment, cells were treated with 500 µM of Cys and 25 µM of ABIA separately and were allowed to incubate for 1 h at 37 °C and 5% CO2 and were then washed three times with 0.1 M PBS (0.5 mL) before observation. For the bio-imaging of Cys by ABIA, cells were incubated with 500 µM of Cys for 1 h followed by replacing the media containing 25 µM of ABIA and incubating the cells for another 1 h. Then, the cells were washed three times with 0.1 M PBS (0.5 mL) before observation. For another control experiment, cells were treated with 1 mM Nethylmaleimide (NEM, a biothiol scavenger) for 30 min at 37 °C followed by washing three times with 0.1 M PBS (0.5 mL). Then, the cells were incubated in the presence of 25 µM of ABIA for 1 h followed being washed three times with 0.1 M PBS (0.5 mL) before observation. In a similar experiment, cells pre-tread with NEM (1 mM), as mentioned above, were treated with Cys (500 µM, for 1 h) followed being washed with 0.1 M PBS (0.5 mL × 3) and then incubated in the presence of ABIA (25 µM, 1 h) and finally being washed three times 0.1 M PBS (0.5 mL) before observation. Finally, the PBS (1 mL) was added to each glassbottom culture dish, and then the fluorescence images were recorded using a confocal microscope (Carl Zeiss LSM710).

The probe ABIA was synthesized in a two-step reaction as depicted in Scheme 1. In the first step, a simple yet efficient method for the synthesis of compound 3 was developed. The reaction of 4-methylbenzene-1,2-diamine (4.0 mmol) and anthracene-9carbaldehyde (4.0 mmol) in ethanol at room temperature in the presence of O2 from the air and visible light allowed us to afford compound 3 with 80% yield (see the Supplemental Information Figures S1-S3) . To the best of our knowledge, this is a first report on the synthesis of compound 3. The reported synthetic procedures to obtain benzimidazole derivatives are different than the one employed here [39, 40] . The previously reported methods used stringent reaction conditions, including dimethyl sulfoxide as a solvent, the Scheme 1. Scheme for the synthesis of the probe ABIA.

In the first step, a simple yet efficient method for the synthesis of compound 3 was developed. The reaction of 4-methylbenzene-1,2-diamine (4.0 mmol) and anthracene-9carbaldehyde (4.0 mmol) in ethanol at room temperature in the presence of O 2 from the air and visible light allowed us to afford compound 3 with 80% yield (see the Supplemental Information Figures S1-S3) . To the best of our knowledge, this is a first report on the synthesis of compound 3. The reported synthetic procedures to obtain benzimidazole derivatives are different than the one employed here [39, 40] . The previously reported methods used stringent reaction conditions, including dimethyl sulfoxide as a solvent, the temperature of 110 • C, and I 2 as a catalyst. It is important to note that the procedure employed here uses mild reaction conditions, including ethanol as a solvent and 25 • C without using the additional catalyst. The method presented here allowed the synthesis of compound 3 with comparable yield.

In a second step, compound 3 was reacted with the prop-2-enoyl chloride (1.29 mmol) in the presence of triethylamine (1.29 mmol) and DMAP (0.033 mmol) to afford the final compound ABIA (see the Supplemental Information Figures S4-S6 ) in comparable yield.

The 1 H NMR and 13 C NMR spectra of ABIA demonstrate the 5(6)-methyl tautomerism related to the N-substituted benzimidazoles (see the Supplemental Information Figure S7 and Table S1 ). According to previous reports, the tautomerism in benzimidazole derivatives is a well-known phenomenon, and in most cases, the separation of tautomers by column chromatography is not feasible [41, 42] . Hence, we used the tautomeric mixture of ABIA in further experiments. The photophysical properties of compound 3 (10 µM) and probe ABIA (10 µM) in 90% DMSO:0.01 M HEPES buffer solution did not indicate a significant effect of tautomerism in ABIA. As shown in Figure 1 , the optical absorbance spectrum of compound 3 shows λ ex at 368 nm and another two peaks at 353 nm and 388 nm. The emission spectra of compound 3 show λ em at 475 nm (λ ex = 368 nm), indicating Stoke's shift of 107 nm. Similarly, the probe ABIA demonstrates three distinct peaks (356, 372, and 392 nm) with the absorption maxima at 372 nm. Interestingly, ABIA showed fluorescence (λ em = 453 nm) that was almost 30-fold lower than compound 3, indicating that the intramolecular charge transfer induced fluorescence quenching due to the N1-substituted acrylate group. The acrylate group has a strong electron-withdrawing ability that enhances the fluorescence turn-off effect in ABIA.

These results indicate that reaction-induced removal of the acrylate group in ABIA can result in compound 3 with the fluorescence turn-on effect. Hence, the spectral characteristics of compound 3 were studied using various ratios (10, 50, 70, and 90%) of the DMSO:0.01 M HEPES buffer solution. As shown in Figure S8 and Table S2, 

The selectivity of the probe ABIA for Cys detection was investigated using fluorescence spectroscopy. The fluorescence spectra of ABIA (10 µM, in 90% DMSO:0.01 M HEPES buffer solution) were recorded immediately (1 min) after adding the five equivalents of various amino acids, BSA, anions (Cl − , Br − , NO 3 − , AcO − , SO 4 2− , PO 4 3− ), and cations (Na + , Cs + , Ca 2+ , Cu 2+ ) to the solution containing ABIA. As shown in Figure 2a , ABIA showed negligible fluorescence. However, the fluorescence intensity of ABIA increased significantly in the presence of Cys (λ em = 455 nm) compared to the other analytes. Among the mercapto group-containing amino acids, ABIA showed 6-fold and 15-fold higher se-lectivity for Hcy (λ em = 460 nm) and GSH (λ em = 475 nm), respectively. In contrast, the selectivity for Cys was 50-fold higher than other amino acids. Further, ABIA did not show any interaction with biologically relevant ions such as Cl − , Br − , NO 3 − , AcO − , SO 4 2− , PO 4 3− , Na + , Cs + , Ca 2+ , and Cu 2+ . As shown in Figure 2b , in competition experiments conducted in the presence of an excess of (five equivalents) other amino acids, including Hcy and GSH, ABIA did not show any interference in the detecting Cys. However, among the tested biologically relevant ions, only Cu 2+ affected the detection of Cys at tested equimolar concentrations (50 µM). Cys forms a coordination complex with Cu 2+ ions using the mercapto and carboxylate functional groups [43] . Therefore, the complexation of Cys with Cu 2+ inhibits its nucleophilic addition ability to the acrylate group of ABIA. However, the amount of Cu 2+ (180 nM) [44] is negligible compared to Cys in healthy human urine (120 µM) and in the urine of cystinuria patients (2000 µM) [45, 46] . Thus, Cu 2+ would not interfere in Cys detection using the probe ABIA in the actual urine sample. These results indicate that ABIA is a highly selective fluorescence turn-on probe for Cys, and it can be applied to detect intracellular and urinary Cys. To estimate the minimum response time, we traced the time-dependent fluorescence intensity of ABIA (10 µM) for 60 min upon the addition of five equivalents of Cys, as shown in Figure S9 . The fluorescence intensity almost reached the maximum (310 a.u.) in 10 min after the addition of Cys. It is important to note that the fluorescence intensity was 121 a.u. within 1 min after adding Cys, which was comparatively fast compared to the reported probes, considering the structural simplicity of ABIA (see the Supplemental Information Table S3 ). In addition, we calculated the pseudo-first-order rate constants of the reactions between ABIA (10 µM) and five equivalents of Cys. The calculated pseudo-first-order rate constants for Cys from the linear regression analysis of time-dependent changes in the fluorescence intensity was 5.13 × 10 −3 s −1, as shown in Figure S9 . These results indicate that the ABIA shows high specificity for Cys and a short reaction time (1 min). Hence, ABIA is applicable for the detection and quantification of Cys in urine and live cells.

The Cys detection mechanism by ABIA was studied using 1 H NMR spectroscopy and mass spectroscopy. As shown in Figure 3 Figure 3b . The formation of compound 3 after the reaction of ABIA with Cys indicates the resultant fluorescence "turn-on" mechanism. Further proof for the proposed mechanism presented in Figure 3b was deduced from the mass spectra of a reaction product obtained by reacting equimolar ABIA and CYS for 60 min at 25 • C in 90% DMSO:0.01 M HEPES buffer solution. The solvent was evaporated at 40 • C under high-vacuum, and the resultant residue was prepared for the acquisition of the mass spectra by dissolving it in methanol. As presented in Figure 3b and Figure The Cys detection mechanism by ABIA was studied using 1 H NMR spectroscopy and mass spectroscopy. As shown in Figure 3 , 0.5 and 1.0 equivalents of Cys were added to the 90% DMSO:0.01 M HEPES buffer solution (DMSO-d6 and D2O were used to make this solution) containing ABIA. Upon reaction, the peaks at 5.26, 5.71, and 5.97 ppm corresponding to the acrylate group of ABIA completely disappeared with 1.0 equivalents of Cys. These results indicate that the mercapto group in Cys undergoes the Michael addition with the double bond in the acrylate group of ABIA. Further, the appearance of new peaks at 2.26, 2.34, and 3.05 ppm indicates the intramolecular attack of the amine group of Cys on the carbonyl of ABIA, resulting in the cyclized product along with compound 3, as shown in Figure 3b . The formation of compound 3 after the reaction of ABIA with Cys indicates the resultant fluorescence "turn-on" mechanism. Further proof for the proposed mechanism presented in Figure 3b was deduced from the mass spectra of a reaction product obtained by reacting equimolar ABIA and CYS for 60 min at 25 °C in 90% DMSO:0.01 M HEPES buffer solution. The solvent was evaporated at 40 °C under highvacuum, and the resultant residue was prepared for the acquisition of the mass spectra by dissolving it in methanol. As presented in Figure 3b and Figure 

A schematic of the CysDDev prototype is shown in Figure 4 . The LED was arranged in a nozzle opening at a 90 • angle to the sensor nozzle in the cuvette holder, allowing efficient sample illumination by UV LED and detecting emitted light by the sensor. An electric current of 15 mA was delivered to the UV LED (λ = 370 nm) under a bias of 9 V using a rechargeable Li-ion battery. The analog signals from the sensor consisted of a train of pulses correlating to the spatial position of 256 pixels corresponding to wavelengths in the range of 340-850 nm. The analog data collected from the analog pin of the sensor were digitized in a bit resolution of 10 bits using the Arduino Uno R3 microcontroller that sends the processed data to the computer. The final data of individual sample readings were saved as a Microsoft Excel file (.csv) in the pre-selected folder on the connected computer. We compared the performance of CysDDev with the commercial fluorescence spectrometer using the ABIA (10 µM) and compound 3 (10 µM) in 90% DMSO:0.01 M HEPES buffer solution. As shown in Figure 5a , the CysDDev showed comparable results with the commercial fluorescence spectrometer for compound 3 and the probe ABIA. These results indicate that the CysDDev developed here can detect Cys in various solutions, including in urine. 

The effect of pH (pH = 3-10) on the detection of Cys using ABIA was examined by using CysDDev both in the absence and presence of Cys (50 µM) in simulated human urine, as shown in Figure 5b . The fluorescence intensity of the probe ABIA in the absence of Cys did not show a significant change in the studied pH range of 3-10, indicating that the ABIA has remarkable stability in acidic and alkaline environments. The fluorescence intensity increased in the presence of various concentrations of Cys from pH 3.0-10.0. The pKa values of the Cys for α-NH 3 + (pKa = 10.25) and -SH (pKa = 8.0) groups dictate that below pH 8, the -SH is the only nucleophile reacting with the acrylate group of ABIA. However, over pH 8, the nucleophilicity of Cys α-NH 2 increases. Hence, over pH 8, the -SH and -NH 2 groups of Cys can react with ABIA and can enhance the de-acrylation process, resulting in higher fluorescence intensity with increasing pH. Unlike reported probes for Cys detection that require use at pH ≥ 9.0 [47] [48] [49] , ABIA can detect Cys in the physiological pH range and the typical urine pH values of 6.0 to 7.5.

Cys detection using ABIA and CysDDev was performed using urine with a pH of 7.4. As shown in Figure 6 , a calibration plot (0-150 µM) was obtained by diluting a stock solution of Cys. As depicted in Figure 6 , the fluorescence signals of ABIA (10 µM) increase linearly upon the successive addition of Cys until 20 µM and then reach the plateau around 50 µM and remains the same until 150 µM. The LOD for detecting Cys by ABIA using CysDDev was found to be 16.3 nM, with a linear detection range of 0-20 µM. It is imperative to note that ABIA demonstrated relatively lower detection limits for Cys than the other methods presented in Table S4 .

Here, we used the standard addition method to quantify the Cys in the urine sample of a healthy volunteer to minimize the interference from the urine components. The fresh urine sample without any pretreatment was spiked with 3, 6, and 9 µM of Cys, and the spiked recovery was measured using the standard curve (Figure 6b (inset) ). The results of the spike test are presented in Table 1 . As shown in Table 1 , the probe ABIA and CysDDev can effectively detect the Cys in the real urine sample with statistically significant recovery (99.20-104.9%) and precision (RSD < 1.45%). 3.6. Cell Imaging Application of ABIA for the Detection of Cys

The MTT assay allowed us to estimate cytotoxicity by treating cells with 0.1, 10, 25, and 50 µM of ABIA, Cys, and ABIA + Cys for 24 h using DMSO as a control. The cytotoxicity assay results are depicted in Figure 7a as the percent cell growth after treatment with ABIA, Cys, and ABIA + Cys compared to the control. There was no significant cell death even after 24 h of treatment at all tested concentrations. Therefore, 25 µM of ABIA was used for the cell imaging applications. As shown in Figure 7b , the control cells, cells treated Cys (500 µM), and cells pretreated with NEM (1 mM) followed by treatment with ABIA (25 µM) did not show significant fluorescence. However, the fluorescence intensity was observed upon the treatment of cells with Cys (500 µM) followed by ABIA (25 µM). Further, the fluorescence intensities were also observed in the cells pretreated with NEM (1 mM) followed sequentially by the treatment of Cys (500 µM) and ABIA (25 µM). These results indicate that the fluorescence turn-on probe ABIA has high potential in biological applications detecting intracellular Cys in the in vitro assays. 

There are several reports on the methods that are developed for detecting biothiols. Fluorescence turn-on sensors have attracted attention because of their high sensitivity, ease of operation, and fluorescence imaging in living cells. The Michael addition reaction [50] , cyclization with aldehydes [51] , conjugate addition-cyclization reaction [52] , cleavage of sulfonamide, sulfonate esters [53] , etc., reaction mechanisms have been reported for Cys detection among these sensors.

Most of the reported Cys detection probes are based on the coumarin scaffold with larger and more complicated structures [54, 55] . Therefore, developing a synthetically accessible fluorescent probe with a simple design that shows high sensitivity and selectivity for detecting Cys can demonstrate several applications. Among the various fluorescent probes used for detecting biothiols, acrylate groups provide a fast response to the mercapto group and have a higher ability to quench fluorescence due to their strong electron-withdrawing effect [43, 56, 57] . Further, there are a few benzimidazole derivatives, such as fluorescent chemosensors [58, 59] . However, in most cases, the benzimidazole moiety demonstrates fluorescence in the UV region (λ em < 400 nm) [60] , which is not suitable for live-cell imaging applications. The probe ABIA presented here contains an anthracene moiety, due to which it demonstrates fluorescence in the visible region, unlike other reported benzimidazole derivatives.

Compound 3, which was presented in this manuscript, exhibited high fluorescence, upon which the subsequent reaction with acryloyl chloride resulted in the non-fluorescent ABIA. The directly linked acrylate group to the benzimidazole skeleton triggered an intramolecular charge transfer (ICT), resulting in a fluorescence turn-off effect. However, the Michael addition of the Cys mercapto group to the acrylate of ABIA restricted the ICT process and results in a fluorescence turn-on effect. ABIA shows selectivity for Cys over Hcy, probably because the rection of ABIA with Cys generates a seven-membered ring. In comparison, a reaction of ABIA with Hcy would produce an eight-membered ring. The strain in an eight-membered ring is much higher than that in a seven-membered ring; thus, a favorable seven-membered ring product forms easily. ABIA demonstrated high selectivity and comparatively fast response time for Cys detection (see the Supporting Information Table S3 ). The live-cell imaging study presented here provides evidence that ABIA has high applicability for in vitro bioimaging for Cys.

Reported probes were used for either the bioimaging or detection of Cys in serum samples. Only a few reports elaborate upon Cys detection in urine. However, the probe ABIA presented here was evaluated for its dual application for detecting Cys in live cells and urine. The CysDDev explained here allows the efficient detection of Cys in simulated human urine. The LOD for Cys detection by the probe ABIA using CysDDev was found to be of 16.3 nM. The CysDDev and ABIA demonstrated excellent clinical applicability in terms of LOD for Cys detection compared to reported methods (see the Supporting Information Table S4 ). Though the further evaluation of CysDDev for clinical application is required, these initial results indicate that CysDDev is an excellent portable tool that is deployable in resource-limited settings. The portability and the ease of use make CysDDev a perfect point-of-care device for evaluating clinical samples.

The novel fluorescence "off-on" probe ABIA to detect the mercapto-group containing amino acids was designed and synthesized. In addition, a portable device, CysDDev, was also designed and developed to measure the Cys in urine. The probe ABIA and CysDDev exhibited highly sensitive, simple, rapid, and inexpensive cysteine detection ability. The acrylate group in ABIA reacted with the mercapto group in Cys by means of the Michael addition reaction mechanism. The Michael addition reaction was followed by selective intramolecular nucleophilic substitution, ensuring selective detection of Cys over Hcy and GSH. The response time of 1 min and a detection limit of 16.3 nM signifies the high clinical applicability of ABIA and CysDDev. Further, ABIA also demonstrated its utility in detecting intracellular cysteine, making it an excellent probe for bio-imaging assay.

These results suggest that the ABIA and CysDDev will provide new insights into developing convenient approaches in Cys and other biomarker detections through simple, accurate, and portable health products for potential biological applications.

Supplementary Materials: The following are available online at https://www.mdpi.com/article/10 .3390/bios11110420/s1, Figure S1 : 1 H-NMR spectrum of compound 3, Figure S2 : 13 C-NMR spectrum of compound 3, Figure S3 : HR-mass spectrum of compound 3, Figure S4 : 1 H-NMR spectrum of ABIA, Figure S5 : 13 C-NMR spectrum of ABIA, Figure S6 : HR-mass spectrum of ABIA, Figure S7 : Structures of the probe ABIA tautomer's A and B, Figure S8 : (a) UV-vis absorbance spectra, (b) Fluorescence spectra of compound 3 in 10, 50, 70, and 90% DMSO:0.01 M HEPES buffer solution (λ ex = 368 nm), Figure S9 : (a), (b)Time-dependent fluorescence response and (c) pseudo-first-order kinetic plots of ABIA (10 µM) reaction with Cys (50 µM) in 90% DMSO:0.01 M HEPES buffer solution (λ ex = 368 nm, λ em = 455 nm), Figure S10 : Mass spectra of a reaction product obtained by reacting equimolar ABIA and Cys for 60 min at 25 • C, Table S1 : 1 H NMR and 13 C NMR chemical shifts (δ ppm) of the ABIA tautomer's A and B, Table S1. 1 H NMR and 13 C NMR chemical shifts (δ ppm) of the ABIA tautomer's A and B; Table S2 : Photophysical properties of compound 3 (10 µM) in varying percentages of DMSO:0.01 M HEPES buffer solution, Table S3 : A comparison of response time for cysteine detection by various methods, Table S4 : A comparison of different probes used for cysteine detection. 

The data presented in this study are available upon request from the corresponding author.

The authors declare no conflict of interest.

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