Development of a Tri-Functional Nanoprobe for Background-Free SERS Detection of Sialic Acid on the Cell Surface

: Sialic acid (SA) on the surface of cells is indispensable in numerous physiological and pathological processes, and sensitive and reproducible detection of SA is crucial for diagnosis and therapy in many diseases. Here, we developed a tri-functional nanoprobe as a sensitive and straightforward surface-enhanced Raman spectroscopy (SERS) nanoprobe for sialoglycan detection on cell surfaces. The reporter was designed to provide three key functionalities that make it ideal for SA detection. First, we employed two recognition groups, phenylboronic acid and an ammonium group, that enhance SA recognition and capture efﬁciency. Second, we used cyano as the Raman reporter because it emits in the cellular Raman silent region. Finally, thiol acted as an anchoring agent to conjugate the reporter to silver nanocubes to provide SERS enhancement. Our molecular nanoprobe design demonstrated the ability to detect SA on the cell surface with high sensitivity and spatial resolution, opening up new routes to cellular diagnostics.


Introduction
Sialic acid (SA), also known as N-acetylneuraminic acid, is an acidic monosaccharide with a nine-carbon backbone and is typically located at the outermost end of cell surface glycoproteins. Because of its location and ubiquitous distribution, SA is pivotal in mediating and modulating numerous physiological and pathological activities, such as cell-cell communication, intercellular adhesion, immunological responses, cancer metastasis, and bacterial and viral infections [1]. Furthermore, SA serves as a binding site for various pathogens and toxins [2,3], and changes in SA level and expression usually signal pathological conditions. For example, overexpression of SA on the cell surface is linked to malignancy and cancer metastasis [4]. Several SA-containing carbohydrate antigens have been identified as cancer biomarkers that are useful for early stage diagnosis and effective prognosis during treatment [5][6][7].
Surface-enhanced Raman spectroscopy (SERS) is a powerful detection tool with great potential for diagnostics because of advantages that include simple sample preparation,

Instruments and Characterization
The size and morphology of AgNCs were characterized by employing scanning electron microscopy (SEM) (FEI NOVA-600), operated at an accelerating voltage of 15 kV. The X-ray diffraction (XRD) pattern was recorded using a Bruker D8 advance X-ray diffractometer, 2θ from 35 • to 90 • with a scan rate of 0.05 degrees per step. UV-Vis absorption spectra were acquired using Perkin Elmer Enspire Multimode Plate Reader. The spectra were recorded from 300 nm to 900 nm in steps of 1 nm. Dynamic light scattering (DLS) and zeta potential were determined using a Zeta sizer Nano ZS (Malvern Instruments, Malvern, UK) equipped with a 633-nm laser. Disposable folded capillary cells (Malvern DT1070) were used to perform the measurements, and the data analysis was done using Zetasizer software. For particle size, we report the z-average diameter (the mean hydrodynamic diameter), and zeta-potential values were estimated from the measured electrophoretic mobility data using the Smoluchowski equation (Malvern Instruments Ltd., Malvern, UK). 1 H NMR (nuclear magnetic resonance) spectra were recorded on a Bruker AVII-500 (500 MHz) spectrometer with the H 2 O peak in CD 3 OD (δ H = 4.87 ppm) as an internal standard. 13 C NMR spectra were recorded on an AVII-500 (125 MHz) spectrometer using CD 3 OD (δ C = 49.15 ppm, central line of a septet) as the internal standard. Structural assignments were made with additional information from 2-D homonuclear correlation spectroscopy, 2-D heteronuclear multiple-quantum correlation spectroscopy, and 2-D heteronuclear multiple-bond correlation spectroscopy experiments using gradient pulses for coherence pathway selection, which were acquired on a Bruker AVII-500 spectrometer. High-resolution mass spectroscopy (HRMS) data were generated using a Bruker Bio-TOF III (ESI-TOF) or Bruker Ultraflex (i.e., MALDI-TOF/TOF) spectrometer and are reported as mass/charge (m/z) ratios with percentage relative abundance. Analytical thin-layer chromatography was performed on pre-coated glass plates of thin layer chromatography Silica gel 60 F 254 from Merck. For detection, we used UV-Vis (254 nm) and/or staining with reagents containing ceric molybdate (for general use) or ninhydrin (for samples containing amino groups). Raman and SERS spectra were obtained from a home-built micro Raman system with 532-nm laser excitation at room temperature (RT).

Synthesis of AgNCs
AgNCs were synthesized via the polyol method using CF 3 COOAg as the silver precursor and EG as the solvent and reducing agent. A total of 5 mL of EG was heated at 150 • C without reflux for 40 min under mild stirring. NaHS (3 mM in EG, 60 µL) was added into the heated EG. After 2 min, HCl (3 mM in EG, 450 µL) was then rapidly injected into the heated solution, followed by the addition of PVP (20 mg/mL in EG, 1250 µL). After another 2 min, CF 3 COOAg (282 mM in EG, 400 µL) was injected into the mixture. The mixture was kept at 150 • C for 1 h and then quenched by placement in an ice-water bath. The product was centrifuged at 12,000 rpm for 20 min at 20 • C and washed with acetone (1×) and ethanol (2×) to remove the excess EG and PVP, respectively. The product AgNCs with an edge length of~48 nm were re-dispersed in 3 mL isopropanol and stored at 4 • C for further use. The characterization of synthesized AgNCs was done by UV-Vis spectroscopy, XRD, and SEM.  Oxyma (282 mg, 1.98 mmol) and N,N'-DIC (282.4 µL, 1.8 added to a solution of compound 2 (350 mg, 1.80 mmol) and Fm g, 1.80 mmol) in dimethylformamide (DMF) (18.04 mL) at 0 °C was allowed to stir at 4 °C for 24 h. Then, the reaction mixtu (30 mL), followed by a wash with ddH2O (50 mL, 2×) and satu mL, 2×). The EtOAc layer was collected, dried over MgSO4, fi evaporation to afford a viscous yellow crude. The crude was p tography on silica gel with EtOAc/MeOH/H2O (14/2/1, v/v) to y uct 3 (440.4 mg, 32%) as a yellow oil.

Synthesis of Tri-Functional Nanoprobe (Reporter 6 Conjugated AgNCs)
The nanoprobe was obtained by conjugation of reporter 6 onto the AgNC surface through an Ag-S bond. Briefly, 100 µL AgNC colloid solution was added to 1 mL of 4 mM reporter 6 and vigorously stirred for 1.5 h. The unbound reporter 6 was removed by centrifugation at 9000 rpm for 10 min. The conjugate of AgNC-reporter 6 was then dispersed in 50 µL sterile water for further experiments. The nanoprobe was freshly prepared before its addition into fixed cells for Raman measurements. The DLS and zeta potential were used to certify the nanoprobe.

Cell Culture and Treatment with Nanoprobe
HeLa cells and Hs68 cells (1 × 10 5 ) were cultured on silicon wafers placed inside a 24-well plate, respectively, in Dulbecco's modified Eagle medium, supplemented with 10% (v/v) fetal bovine serum and 1% (v/v) penicillin-streptomycin, at 37 • C in an incubator containing 5% CO 2 . After 3 days, the cells were washed 3 times with Dulbecco's phosphatebuffered saline (DPBS), fixed with 4% (w/v) formaldehyde at RT for 20 min, then rinsed with DPBS (3×). Next, the fixed HeLa cells and Hs68 cells, respectively, incubated in 250 µL DPBS per well, were treated with 10 µL nanoprobe for 2 h. Subsequently, the fixed HeLa cells and Hs68 cells on silicon wafers were washed with DPBS 3 times to remove unbound nanoprobe before Raman measurements.

Specificity of Nanoprobe towards SA
Nanoprobe (10 µL) was mixed with 1 mL (0.5 µM) aqueous solution of each free monosaccharide (glucose, mannose, galactose, and sialic acid) and stirred for 1 h. Then, the solution was centrifuged at 9000 rpm for 10 min to remove the unbound monosaccharides, resulting in glucose-pretreated nanoprobe, mannose-pretreated nanoprobe, galactosepretreated nanoprobe, and sialic acid-pretreated nanoprobe, respectively. The monosaccharidepretreated nanoprobes were added onto fixed HeLa cells on silicon wafers and incubated for 2 h at RT. The HeLa cells on the silicon wafer then were rinsed with DPBS (3×) to wash out the unbound nanoprobe, followed by Raman measurement.
For experiments with PBA, fixed HeLa cells were pretreated with 0.04 mM and 0.4 mM of PBA for 1.5 h at RT, followed by rinsing with DPBS (3×) to eliminate unbound PBA. After that, the fixed HeLa cells, incubated in 250 µL DPBS per well, were treated with 10 µL nanoprobe for 2 h at RT. The cells were then washed 3 times with DPBS to wash away the unbound nanoprobe prior to Raman measurements.
The experiment using sialidase to cleave the sialic acid on the cell surface was done by pretreating fixed HeLa cells with 20 mU sialidase (from Arthrobacter ureafaciens) in sialidase buffer (20 mM HEPES-NaOH, pH 7.0, 140 mM NaCl) for 2 h at RT. After that, the cells were washed with DPBS (3×) to remove the free sialic acid, followed by treatment of the cells with 10 µL nanoprobe in 250 µL DPBS per well at RT. After 2 h, the cells were washed with DPBS (3×) to wash out the unbound nanoprobe prior to SERS measurements.

SERS Measurement
SERS spectra were acquired using a home-built confocal micro Raman system with 532-nm laser excitation at RT. A laser power of 0.7 mW and acquisition time of 5 s were used. Silicon wafers, which were used in cell culture, were sterilized under UV light for 1 h before cell experiments. ORIGINLAB software (Northampton, MA, USA) was used for SERS spectra baseline correction. SERS imaging of a single HeLa cell was acquired by a point-mapping method with 1.0-µm steps using a 532-nm laser, 0.7-mW power laser, 100× objective lens (numerical aperture 0.85), and 1-s exposure time. The SERS signal of cyano at 2230 cm −1 was chosen for generating the SERS mapping image using MATLAB (MathWorks) program.

Synthesis and Characterization of AgNCs
We prepared AgNCs as SERS substrate to amplify the Raman signal, due to their advantages over other nanoparticles. First, noble metal nanostructures such as silver (Ag), gold (Au), and Au-Ag bimetallic nano alloys [19] have been widely used as SERS substrates. However, Ag nanostructures exhibit stronger Raman enhancement rather than Au nanostructure in visible spectrum, because Ag provides higher efficiency of plasmon excitation, and interacts more efficiently with visible light. The light-interaction crosssection for Ag can be about ten times higher than that of the geometric cross-section, indicating that the Ag captures more light than is physically irradiated on them [20,21]. Moreover, the cost of Ag is lower than that of Au. Second, nanoparticles generate greater SERS enhancement if they contain sharp features on their surface (like nanocubes). The calculated electromagnetic enhancement from nanocube is about 100 times higher than nanosphere due to the oscillation of surface electrons, which are confined to the corners of nanocubes [22]. Finally, AgNCs can be prepared in a large scale with high monodispersity and reproducibility.
AgNCs were synthesized by the polyol method and characterized by SEM, UV-Vis, XRD, DLS, and zeta potential measurements (Figures 1 and 2). Upon optimization, the morphology of the silver nanoparticles was shown to be cubic, with an edge length of 48 nm (Figure 1a). The XRD pattern of AgNCs confirmed the presence of highly crystalline silver nanoparticles. Five main characteristic diffraction peaks at 38.10 • , 44.28 • , 64.40 • , 77.39 • , and 81.56 • were assigned as (111), (200), (220), (311), and (222) lattice planes, and accordingly indexed as face-centered cubic structures based on JCPDS file No. 04-0783 ( Figure 1b). Additionally, the UV-Vis spectra of AgNCs indicated the typical surface plasmon resonance feature of a cubic silver nanostructure with a major band at 435 nm and two shoulders at 349 and 389 nm, corresponding to a dipolar, octupolar, and quadrupolar peak, respectively, in agreement with the existing studies (Figure 1c) [23,24]. enhancement if they contain sharp features on their surface (like nanocubes). The calculated electromagnetic enhancement from nanocube is about 100 times higher than nanosphere due to the oscillation of surface electrons, which are confined to the corners of nanocubes [22]. Finally, AgNCs can be prepared in a large scale with high monodispersity and reproducibility.
AgNCs were synthesized by the polyol method and characterized by SEM, UV-Vis, XRD, DLS, and zeta potential measurements (Figures 1 and 2). Upon optimization, the morphology of the silver nanoparticles was shown to be cubic, with an edge length of ~48 nm (Figure 1a). The XRD pattern of AgNCs confirmed the presence of highly crystalline silver nanoparticles. Five main characteristic diffraction peaks at 38.10°, 44.28°, 64.40°, 77.39°, and 81.56° were assigned as (111), (200), (220), (311), and (222) lattice planes, and accordingly indexed as face-centered cubic structures based on JCPDS file No. 04-0783 ( Figure 1b). Additionally, the UV-Vis spectra of AgNCs indicated the typical surface plasmon resonance feature of a cubic silver nanostructure with a major band at 435 nm and two shoulders at 349 and 389 nm, corresponding to a dipolar, octupolar, and quadrupolar peak, respectively, in agreement with the existing studies (Figure 1c) [23,24].

Design and Synthesis of Reporter
To provide a reliable and straightforward nanoprobe for detection of SA-containing glycans on the cell surface, we designed a reporter (6 in Scheme 1). Cyano was chosen for a characteristic Raman signal because its vibrational Raman spectrum falls in a cellular Raman silent region (1800-2800 cm −1 ), allowing for background-free SERS detection without interference from naturally existing biomolecules in cells [11,13].

Design and Synthesis of Reporter
To provide a reliable and straightforward nanoprobe for detection of SA-containing glycans on the cell surface, we designed a reporter (6 in Scheme 1). Cyano was chosen for a characteristic Raman signal because its vibrational Raman spectrum falls in a cellular Raman silent region (1800-2800 cm −1 ), allowing for background-free SERS detection without interference from naturally existing biomolecules in cells [11,13].

Design and Synthesis of Reporter
To provide a reliable and straightforward nanoprobe for detection of SA-containing glycans on the cell surface, we designed a reporter (6 in Scheme 1). Cyano was chosen for a characteristic Raman signal because its vibrational Raman spectrum falls in a cellular Raman silent region (1800-2800 cm −1 ), allowing for background-free SERS detection without interference from naturally existing biomolecules in cells [11,13].

Scheme 1. Synthesis of reporter 6.
PBA has been known to selectively bind to SA over other sugars at physiological pH or under weakly acidic pH conditions [25]. The binding between PBA and various sugars Scheme 1. Synthesis of reporter 6.
PBA has been known to selectively bind to SA over other sugars at physiological pH or under weakly acidic pH conditions [25]. The binding between PBA and various sugars at physiological pH was reported with the association constant in decreasing order of PBA to SA >> galactose > mannose > glucose [26]. Furthermore, a positively charged ammonium group increased the binding of the phenylboronate/ 160 Tb with SA at physiological pH because of the electrostatic interaction with the SA carboxyl group [27]. Therefore, to enhance selective binding towards SA, we incorporated an ammonium group to bind with the negative charge of the SA carboxylate group, in addition to the covalent binding of boronic acid to SA (i.e., formation of boronate ester with the two hydroxyl groups on C 7 -C 9 or C 8 -C 9 of SA) [28].
Because it is crucial to have strong reporter binding on the surface of nanoparticles to achieve extensive SERS enhancement, thiol was employed to attach the reporter to the nanoparticle surface by chemisorption. Of note, thiol has a stronger binding to Ag nanoparticles in comparison with other functional groups (e.g., amines, alcohols, and carboxylic acids) [29]. Additionally, thiol has been used to prevent oxidation of Ag nanoparticles, maintain their usability on SERS sensing, and lower its toxicity. It was found that molecules containing a thiol moiety could block the Ag nanostructures surface, quantitatively inhibit any oxidation through strong binding of thiol group to the Ag nanostructures surface [30,31], and thus usefully maintain its high enhancement factor.
The synthesis of reporter 6 is shown in Scheme 1. The synthesis started with a reductive amination between commercially available 3-formylphenylboronic acid and N-Boc-ethylenediamine. First, the solution of 3-formylphenylboronic acid in MeOH was reacted with N-Boc-ethylenediamine at RT to form the imine intermediate, followed by reduction with NaBH 4 , leading to formation of compound 1 at 90% yield in two steps. Next, Boc deprotection was conducted under an acid condition, 4 M HCl in 1,4-dioxane, to give the amine product (2) in quantitative yield. An amide-forming reaction was performed to conjugate 2 with the acid (Fmoc-S-trityl-L-cysteine), in which oxyma was used in the presence of N,N'-DIC. The desired cysteine-conjugated boronic acid derivative (3) was obtained in 32% yield. Further removal of the Fmoc group by stirring 3 in a solution of piperidine in DMF generated compound 4 in 88% yield. Another amide-bonding reaction was conducted by coupling 4 with cyanoacetic acid, resulting in formation of the desirable product (5) in 34% yield after silica gel column chromatography. Final deprotection of S-trityl ether was performed by using trifluoroacetic acid in the presence of TES as a cation scavenger [32,33], leading to the target reporter (6) in quantitative yield. The product was recrystallized in diethyl ether for further studies.

Characterization of Tri-Functional Nanoprobe
The nanoprobe was successfully fabricated by binding 6 to the surface of AgNCs and confirmed by DLS and zeta potential. The DLS data showed that the hydrodynamic size of AgNCs increased from 101.3 nm to 142.0 nm after coating with 6 ( Figure 2a). The zeta potential exhibited a change in surface charge of AgNCs from −27.0 mV (the original AgNCs) to +33.8 mV (the modified AgNCs), as shown in Figure 2b. In addition, Raman measurements confirmed the conjugation of 6 onto the AgNC surface (Figure 2c). In the silent region, a single and strong SERS peak at 2230 cm −1 , corresponding to the cyano moiety, was observed after conjugation of 6 onto the AgNC surface.
Furthermore, the SERS spectrum of the nanoprobe was compared to the Raman spectrum of 6 to verify the conjugation of 6 onto the AgNC surface. It can be seen that the Raman peak at 2565 cm −1 (highlighted in light blue in Figure 2c) in 6, which resulted from the stretching mode of the thiol group, disappeared in the nanoprobe. This result indicated that reporter 6 was successfully chemisorbed onto the AgNC surface as thiolate.
To characterize the sensitivity of AgNCs, solutions of different concentrations of 6 were mixed with a fixed amount of AgNCs, and Raman signal intensity was quantitatively calibrated (Supporting Information Figure S1). We were gratified to see that Raman signal was detectable even at the level of zepto-moles (10 −21 mole) of 6, thus proving the high sensitivity of AgNCs in enhancing the Raman signal of 6.

SA Expression on HeLa Cells
HeLa cells were chosen as a cancer cell model to demonstrate how our nanoprobe can be applied for detecting sialoglycan expression on the cell surface. SA-containing carbohydrates are overexpressed on the surface of HeLa cells. After incubation of the SERS nanoprobe with the fixed HeLa cells for 1 h at RT, the unbound nanoprobe was removed by a rinse with DPBS (3×) to eliminate the nonspecific binding and false-positive signals. The SERS spectra were recorded in the Raman silent region (1800-2800 cm −1 ), based on the finding that the cyano group exhibited a typical SERS peak at 2230 cm −1 . The single and sharp SERS signal at 2230 cm −1 , corresponding to the stretching vibration of cyano, was clearly detected on the surface of HeLa cells (Figure 3a,b). The signal was easy to distinguish and free of background noise. This result confirms the binding of our nanoprobe to HeLa cells.
Meanwhile, we also treated the cells with the bare AgNCs (that did not contain 6) to clarify the binding of nanoprobe and cell. Because there was no reporter attached to the surface of AgNCs, no SERS signal was observed, indicating no binding between the bare AgNCs and HeLa cells (Figure 3c,d).
The SERS spectra were recorded in the Raman silent region (1800-2800 cm −1 ), based on the finding that the cyano group exhibited a typical SERS peak at 2230 cm −1 . The single and sharp SERS signal at 2230 cm −1 , corresponding to the stretching vibration of cyano, was clearly detected on the surface of HeLa cells (Figure 3a,b). The signal was easy to distinguish and free of background noise. This result confirms the binding of our nanoprobe to HeLa cells. Meanwhile, we also treated the cells with the bare AgNCs (that did not contain 6) to clarify the binding of nanoprobe and cell. Because there was no reporter attached to the surface of AgNCs, no SERS signal was observed, indicating no binding between the bare AgNCs and HeLa cells (Figure 3c,d).
To evaluate the specificity of the developed nanoprobe, we pretreated the nanoprobe with a monosaccharide, such as glucose, mannose, galactose, or SA, before applying the nanoprobe to HeLa cells. If any of the monosaccharides were to bind strongly to the nanoprobe, the binding to the SA-containing HeLa cells would be compromised [12]. As shown in Figure 4a,c, the intensity of SERS signals remained mostly high from the HeLa cells that had been incubated with the monosaccharide-pretreated nanoprobe. For example, we observed 77% signal intensity with respect to the control (cells treated with the nanoprobe) from the cells incubated with the glucose-pretreated nanoprobe. Likewise, 74% and 68% intensities were found from the cells incubated with the mannose-and galactose-pretreated nanoprobe, respectively. The results indicated a weak binding of the nanoprobe with glucose, mannose, or galactose, and this low affinity was inferred to leave To evaluate the specificity of the developed nanoprobe, we pretreated the nanoprobe with a monosaccharide, such as glucose, mannose, galactose, or SA, before applying the nanoprobe to HeLa cells. If any of the monosaccharides were to bind strongly to the nanoprobe, the binding to the SA-containing HeLa cells would be compromised [12]. As shown in Figure 4a,c, the intensity of SERS signals remained mostly high from the HeLa cells that had been incubated with the monosaccharide-pretreated nanoprobe. For example, we observed 77% signal intensity with respect to the control (cells treated with the nanoprobe) from the cells incubated with the glucose-pretreated nanoprobe. Likewise, 74% and 68% intensities were found from the cells incubated with the mannose-and galactose-pretreated nanoprobe, respectively. The results indicated a weak binding of the nanoprobe with glucose, mannose, or galactose, and this low affinity was inferred to leave susceptibility to competitive replacement with the high-affinity nanoprobe with the cellsurface sialoglycans. In contrast, there was a dramatic decrease in SERS intensity (only 21% intensity remained) from HeLa cells incubated with the SA-pretreated nanoprobe. Because SA shows strong binding to the SERS nanoprobe, the recognition moiety of the nanoprobe was already saturated with free SA. Therefore, the resulting nanoprobe could not bind to the cellular SA, leading to the observed low SERS signal. Our observed binding trend was also consistent with the above-mentioned binding order of PBA with monosaccharides.
To further examine the specificity of our prepared nanoprobe, we changed the level of available SA on the cell surface in one of two ways: Using PBA to abolish the binding with the cell surface SA, or sialidase (also called neuraminidase, the enzyme that catalyzes the hydrolytic cleavage of SA) to remove SA residues on the cell surface. The expectation was that PBA would strongly bind to SA at physiological pH, allowing for masking of the SA on the cell surface [26]. Consequently, a smaller amount of nanoprobe would attach to the cell surface, and the nanoprobe signal would decrease. As shown in Figure 4b,d, the decreased intensity of the SERS signal was found to be proportional to the increasing concentration of PBA employed to treat HeLa cells. Of note, the intensity of SERS signal was reduced by 77% when there was a prior incubation of HeLa cells with 0.4 mM PBA. Likewise, a reduced intensity of SERS signal was found when HeLa cells were treated with sialidase ( Figure 4b,d), indicating that the reduced signal was the result of the decreased amount of SA on the cell surface.
susceptibility to competitive replacement with the high-affinity nanoprobe with the cellsurface sialoglycans. In contrast, there was a dramatic decrease in SERS intensity (only 21% intensity remained) from HeLa cells incubated with the SA-pretreated nanoprobe. Because SA shows strong binding to the SERS nanoprobe, the recognition moiety of the nanoprobe was already saturated with free SA. Therefore, the resulting nanoprobe could not bind to the cellular SA, leading to the observed low SERS signal. Our observed binding trend was also consistent with the above-mentioned binding order of PBA with monosaccharides. To further examine the specificity of our prepared nanoprobe, we changed the level of available SA on the cell surface in one of two ways: Using PBA to abolish the binding with the cell surface SA, or sialidase (also called neuraminidase, the enzyme that catalyzes the hydrolytic cleavage of SA) to remove SA residues on the cell surface. The expectation was that PBA would strongly bind to SA at physiological pH, allowing for masking of the SA on the cell surface [26]. Consequently, a smaller amount of nanoprobe would attach to the cell surface, and the nanoprobe signal would decrease. As shown in Figure 4b,d, the decreased intensity of the SERS signal was found to be proportional to the increasing concentration of PBA employed to treat HeLa cells. Of note, the intensity of SERS signal was reduced by 77% when there was a prior incubation of HeLa cells with 0.4 mM PBA. Likewise, a reduced intensity of SERS signal was found when HeLa cells were treated with

Examining SA Expression on Normal (Non-Cancerous) and Cancer Cells
To examine the applicability of our SERS nanoprobe, we compared the level of SA expression on normal cell (non-cancerous cell) and cancer cell. HeLa cells were selected as representative cancer cells where the SA expression is high, whereas Hs68 cells were chosen as normal cells containing a basic level of SA expression. As shown in Figure 5, the nanoprobe-treated HeLa cells exhibited a high SERS signal at 2230 cm −1 , in comparison with the signal produced by the nanoprobe-treated Hs68 cells. Furthermore, the SERSsignal intensity from HeLa cells is 4.4 times higher than that from Hs68 cells, confirming the high SA expression on cancer cells. The result is consistent with previous study [13]. Our nanoprobe thus shows a great potential to measure the level of SA expression on cell surface. nanoprobe-treated HeLa cells exhibited a high SERS signal at 2230 cm −1 , in comparison with the signal produced by the nanoprobe-treated Hs68 cells. Furthermore, the SERSsignal intensity from HeLa cells is 4.4 times higher than that from Hs68 cells, confirming the high SA expression on cancer cells. The result is consistent with previous study [13]. Our nanoprobe thus shows a great potential to measure the level of SA expression on cell surface. To directly visualize the location of SA on the surface of Hs68 cell and HeLa cell, we performed Raman mapping experiments. As shown in Figure 6, the Raman signal at 2230 cm −1 , assigned to the cyano moiety of reporter 6, was selected to provide background-free mapping image. The high-resolution mapping images (Figure 6b,d) showed the uneven distribution of SA on the Hs68 and HeLa cell membrane, respectively, which could correlate with the localization and distribution of glycoproteins on the cell membrane. The result is consistent with previous studies [34,35]. Notably, our nanoprobe clearly distinguished the SA expression between non-cancerous ( Figure 6b) and cancer (Figure 6d) cells. The SERS spectra (in Figure 6e), obtained from points 1-3 in the mapping image of HeLa cell (Figure 6d), were free of background interference of cellular Raman signals, leading to a more precise mapping image.  To directly visualize the location of SA on the surface of Hs68 cell and HeLa cell, we performed Raman mapping experiments. As shown in Figure 6, the Raman signal at 2230 cm −1 , assigned to the cyano moiety of reporter 6, was selected to provide backgroundfree mapping image. The high-resolution mapping images (Figure 6b,d) showed the uneven distribution of SA on the Hs68 and HeLa cell membrane, respectively, which could correlate with the localization and distribution of glycoproteins on the cell membrane. The result is consistent with previous studies [34,35]. Notably, our nanoprobe clearly distinguished the SA expression between non-cancerous ( Figure 6b) and cancer (Figure 6d) cells. The SERS spectra (in Figure 6e), obtained from points 1-3 in the mapping image of HeLa cell (Figure 6d), were free of background interference of cellular Raman signals, leading to a more precise mapping image.

Conclusions
SERS offers the potential to detect target molecules in a sensitive and selective manner. This study introduced a simple and reliable tri-functional nanoprobe that combines a Raman reporter, a recognition unit, and a thiol for chemisorption. The tri-functional nanoprobe, 6-conjugated AgNC, allowed for visualization of SA on the HeLa cell surface. This reporter has two beneficial features. The cyano moiety exhibits a single and sharp Figure 6. SA expression on the surface of single Hs68 cell and HeLa cell that were pretreated with nanoprobe. Bright-field (a,c) and SERS mapping (b,d) images of Hs68 cell and HeLa cell, respectively, were generated by the excitation with 532 nm laser (0.78 mW, 100× objective lens, exposure time of 1 s, and step size 1 µm). (e) SERS spectra corresponding to points 1-3 were produced by the SERS mapping image of HeLa cell (d).

Conclusions
SERS offers the potential to detect target molecules in a sensitive and selective manner. This study introduced a simple and reliable tri-functional nanoprobe that combines a Raman reporter, a recognition unit, and a thiol for chemisorption. The tri-functional nanoprobe, 6-conjugated AgNC, allowed for visualization of SA on the HeLa cell surface. This reporter has two beneficial features. The cyano moiety exhibits a single and sharp SERS peak in the cellular Raman silent region, leading to background-free detection. Additionally, boronic acid with the addition of an ammonium group gives enhanced binding toward SA, owing to the combined covalent bond and electrostatic interactions. Because of the reporter, the resulting tri-functional nanoprobe clearly offered the advantages of high sensitivity and background-free detection, paving the way for probing natural sialoglycans on the surface of a single HeLa cell. This nanoprobe thus holds great promise for cancer diagnosis and prognosis.