Au-S Interaction Research Articles

Functional peptide conjugated ordered gold nanoparticles based rational electrochemical immunosensor for highly stable and selective detection of zearalenone

To integrate antifouling properties and good sensitivity on the sensing interface can improve the applicability of an electrochemical immunosensor. These functional regions can be integrated into a single functional peptide (functPP). The rational designed three domains in functPP were the anchoring, antifouling and gold nanoparticles (AuNPs) recognizing domains. Meanwhile, the ordered AuNPs inspired by C15H23CO-RRRRR can be recognized by AuNPs recognizing domains in functPP to enhance the intensity of detecting current. In the sensing system, the anchoring domain in functPP can be immobilized on the Au electrode by AuS interaction, while the antifouling domain undergoes strong hydration with water molecules to resist matrices, and the recognizing domains can directionally capture O-AuNPs to form a functPP-O-AuNPs complex as the core sensing element. Consequently, the complex bound to the monoclonal antibodies against zearalenone by electrostatic adsorption to develop a highly antifouling and sensitive biosensor with the ability to identify zearalenone in cereals.

Engineering ZnIn2S4 with efficient charge separation and utilization for synergistic accelerate dual-function photocatalysis

Combining photocatalytic reduction with organic synthetic oxidation in the same photocatalytic redox system can effectively utilize photoexcited electrons and holes from solar to chemical energy. Here, we stabilized 0D Au clusters on the substrate surface of Zn vacancies modified 2D ZnIn2S4 (ZIS-V) nanosheets by chemically bonding Au-S interaction, forming surfactant functionalized Au/ZIS-V photocatalyst, which can not only synergistic accelerate the selective oxidation of phenylcarbinol to value-added products coupled with clean energy hydrogen production but also further drive photocatalytic CO2-to-CO conversion. An internal electric field of Au/ZIS-V ohmic junction and Zn vacancies synchronously promote the photoexcited charge carrier separation and transfer to optimized active sites for redox reactions. Compared with CO2 reduction in water and the pristine ZnIn2S4, the reaction thermodynamics and kinetics of CO2 reduction over the Au/ZIS-V were simultaneously improved about 11.09 and 45.51 times, respectively. Moreover, the photocatalytic redox mechanisms were also profoundly studied by 13CO2 isotope tracing tests, in situ electron paramagnetic resonance (in situ EPR), in situ X-ray photoelectron spectroscopy (in situ XPS), in situ diffuse reflection infrared Fourier transform spectroscopy (in situ DRIFTS) and density functional theory (DFT) characterizations, etc. These results demonstrate the advantages of vacancies coupled with metal clusters in the synergetic enhancement of photocatalytic redox performance and have great potential applications in a wide range of environments and energy.

Gold Nanoparticle-Decorated Catalytic Micromotor-Based Aptassay for Rapid Electrochemical Label-Free Amyloid-β42 Oligomer Determination in Clinical Samples from Alzheimer's Patients.

Micromotor (MM) technology offers a valuable and smart on-the-move biosensing microscale approach in clinical settings where sample availability is scarce in the case of Alzheimer's disease (AD). Soluble amyloid-β protein oligomers (AβO) (mainly AβO42) that circulate in biological fluids have been recognized as a molecular biomarker and therapeutic target of AD due to their high toxicity, and they are correlated much more strongly with AD compared to the insoluble Aβ monomers. A graphene oxide (GO)-gold nanoparticles (AuNPs)/nickel (Ni)/platinum nanoparticles (PtNPs) micromotors (MMGO-AuNPs)-based electrochemical label-free aptassay is proposed for sensitive, accurate, and rapid determination of AβO42 in complex clinical samples such as brain tissue, cerebrospinal fluid (CSF), and plasma from AD patients. An approach that implies the in situ formation of AuNPs on the GO external layer of tubular MM in only one step during MM electrosynthesis was performed (MMGO-AuNPs). The AβO42 specific thiolated-aptamer (AptAβO42) was immobilized in the MMGO-AuNPs via Au-S interaction, allowing for the selective recognition of the AβO42 (MMGO-AuNPs-AptAβO42-AβO42). AuNPs were smartly used not only to covalently bind a specific thiolated-aptamer for the design of a label-free electrochemical aptassay but also to improve the final MM propulsion performance due to their catalytic activity (approximately 2.0× speed). This on-the-move bioplatform provided a fast (5 min), selective, precise (RSD < 8%), and accurate quantification of AβO42 (recoveries 94-102%) with excellent sensitivity (LOD = 0.10 pg mL-1) and wide linear range (0.5-500 pg mL-1) in ultralow volumes of the clinical sample of AD patients (5 μL), without any dilution. Remarkably, our MM-based bioplatform demonstrated the competitiveness for the determination of AβO42 in the target samples against the dot blot analysis, which requires more than 14 h to provide qualitative results only. It is also important to highlight its applicability to the potential analysis of liquid biopsies as plasma and CSF samples, improving the reliability of the diagnosis given the heterogeneity and temporal complexity of neurodegenerative diseases. The excellent results obtained demonstrate the analytical potency of our approach as a future tool for clinical/POCT (Point-of-care testing) routine scenarios.

Theoretical Study of Au-S Interaction in Clusters Models of a &amp;#945;-cyclodextrin Complex

Theoretical Study of Au-S Interaction in Clusters Models of a &amp;#945;-cyclodextrin Complex

DFT Rationalization of Gold(I)-Catalyzed Couplings between Alkynyl Thioether and Nitrenoid Derivatives: Mechanism, Selectivity Patterns, and Effects of Substituents.

The present work focuses on a theoretical investigation of mechanistic features, chemoselectivity, regioselectivity, and effect of substituents in the gold-catalyzed reactions of alkynyl thioethers and isoxazoles. The DFT calculations reveal that the nucleophilic attack of isoxazole to a β-position of catalyst-bound ynamide forms a vinyl intermediate. This undergoes cleavage of the N-O isoxazole bond and isomerizes to form an α-imino α'-sulfenyl gold carbene complex with stabilization of the Au-S interaction. For 3,5-dimethylisoxazole, the reaction follows a formal [3 + 2] cycloaddition pathway and a 1,3-H migration to give the pyrrole products. Replacement of 3,5-dimethylisoxazole by 3,5-dimethyl-4-phenylisoxazole leads to the formation of deacylative annulation products and desulfenylated 3-acylated pyrroles. Reactions with 4-methyl-3,5-diphenylisoxazoles induce the formation of N-acylated pyrroles and desulfenylated 3-acylated pyrroles. For the minor pathway, the α-addition and 1,2-S migration result in sulfur-substituted β-keto enamide derivatives. In addition, the unique features of regio- and chemoselectivity were rationalized by the distortion and interaction analysis. Apart from fully rationalizing the experimental results, the theoretical DFT data give an important support for comprehending related types of reaction mechanisms.

Citrate functionalized gold nanoparticles assisted micro extraction of L-cysteine in milk and water samples using Fourier transform infrared spectroscopy

This paper describes the sensing application of citrate functionalized gold nanoparticles (AuNPs) employing for the determination of L-cysteine in food and water samples. It is established with diffuse reflectance Fourier transform infrared (DRS-FTIR) spectroscopic analysis. The disappearance of the thiol (-SH) band in the FTIR spectra and the shift in the peaks of the amino group (NH3+) and carboxylate group (–COO-) indicated the Au-S interaction and the aggregation of the NPs. The signal intensity of L-cysteine was enhanced due to hot-spots formed by the aggregation of AuNPs producing the effective absorption of electromagnetic radiation in the IR region for molecular vibration. The relationship between AuNPs and L-cysteine was theoretically investigated by the Density Function Theory (DFT) based on LANL2DZ with the aid of the Gaussian 09 (C.01) software. Interaction between AuNPs and L-cysteine molecules resulted to a shift to higher wavelengths in the plasmon bands, further verified by transmission electron microscopes (TEM), which have indicated random aggregated particles. Further dynamic light scattering (DLS) measurements showed a relatively high degree of polydispersity confirming the aggregation of the particles. Under optimized conditions, the calibration curve showed a good linearity range from 20 to 150 μg mL−1 with a correlation coefficient (R2) 0.990. The limit of detection and quantification were 1.04 and 3.44 μg mL−1, respectively by DRS-FTIR. This modified AuNPs sample was used successfully in milk and water samples with adequate results to determine L-cysteine.

Ultrasensitive SEIRA detection using gold nanobipyramids: Toward efficient multimodal immunosensor

Surface enhanced spectroscopies are proven to be highly efficient in biosensing applications. Their implementation as analytical tools in the detection of medically relevant target analytes demonstrated their ability to considerably decrease the minimum detected analyte concentration, thus showing improved sensitivity compared to commercially available detection kits. In this work, we propose the employment of Surface Enhanced Infrared Absorption (SEIRA), a less exploited analysis tool, for the efficient, specific, and ultrasensitive detection of the biotin-streptavidin recognition interaction using a gold nano-bipyramid-based (AuBPs) immunosensor. The unique optical properties of the AuBPs, such as tunability of the LSPR band ranging from the visible to NIR regions of the spectrum, great absorption capabilities and locally enhanced electromagnetic field at their tips and edges, enable an improved efficiency of the IR absorption of the target analytes. To the as-synthesized AuBPs, a chemically formed p-ATP@biotin recognition element was grafted due to the strong Au-S interaction, followed by the exposure of the obtained biotinylated nanosystem to the streptavidin target analyte. FT-IR experimental measurements as well as theoretical simulations confirm both the successful grafting of the p-ATP@biotin onto the Au surface and successful capture of the target streptavidin protein. A limit of detection of 10−12 M streptavidin concentration was determined, thus standing as a “proof-of-concept” for the development of efficient ultrasensitive SEIRA biosensing devices for more complex biologically relevant applications.

Gold nanocluster surface ligand exchange: An oxidative stress amplifier for combating multidrug resistance bacterial infection

The bacteria redox balance between oxidizing and reducing species plays a critical role in bacterial activities, and the disruption of this homeostasis offers a flexible antibacterial strategy to combat bacterial multidrug resistance. Here, the ligand exchange strategy of Au NCs was first developed to construct an oxidative stress amplifier. We cleverly utilized the reactive oxygen species (ROS) generation ability of histidine (His)-stabilized Au NCs. Cinnamaldehyde (CA) was modified on the surface of Au NCs through an aldimine condensation reaction, and the modification of CA on the surface of Au NCs further accelerated ROS generation. Meanwhile, the strong Au-S interaction between CA-Au NCs and thiols facilitated the ligand exchange of surface histidine-cinnamaldehyde (His-CA) with thiol molecules, causing the consumption of thiols in bacteria and the release of His-CA, which thus finally resulted in efficient bacterial cell death. CA-Au NCs showed excellent antibacterial effects on methicillin-resistant Staphylococcus aureus (MRSA), including 48-h biofilm removal and the treatment of a pig skin wound infection model, representing a promising antibacterial agent for clinical applications.

Determination of soluble CD44 in serum by using a label-free aptamer based electrochemical impedance biosensor.

CD44 is a promising biomarker in the diagnosis and prognosis of malignancies. The serum CD44 level is closely related to disease progression and metastasis of malignancies. It is of great clinical significance for the detection of serum soluble CD44. In this study, a facile, label-free aptamer based electrochemical impedance sensor for serum CD44 has been proposed. The aptamer showing high affinity to CD44 was immobilized on the gold electrodes through Au-S interaction. The interaction between target CD44 and the immobilized aptamer will cause a complex structure change of the aptamer, which makes the diffusion of [Fe(CN)6]3-/4- toward the electrode surface easy, thus resulting in the decrease of the impedance of the system. The decreased degree of the impedance had a good linear relationship with the logarithm of the CD44 concentration in the range of 0.1-1000 ng mL-1 with a detection limit of 0.087 ng mL-1 (S/N = 3). The developed biosensor has been applied to detect CD44 in serum samples with satisfactory results.

Rational Design of Stimuli-Responsive Polymers Modified Nanopores for Selective and Sensitive Determination of Salivary Glucose.

The great pain and stress from finger-prick glucose measurements have resulted in great motivation to find noninvasive glucose monitoring technologies where salivary glucose measurement is desirable. However, the relative low concentration of glucose and coexisting chemicals in saliva challenges the sensitive and selective salivary glucose detection. In this article, we have rationally designed and constructed a salivary glucose sensor by modifying the inner wall of the Au-decorated glass nanopore with stimuli-responsive copolymer poly(3-(acryloylthioureido) phenylboronic acid-co-N-isopropylacrylamide) (denoted as PATPBA-co-PNIPAAm) via Au-S interaction. Notably, upon recognition of glucose, the copolymer could undergo a wettability switch and pKa shifts in the boronic acid functional groups, which significantly regulated the ion transport through nanopores, thus showing improved sensitivity with the detection limit of 1 nM. Moreover, benefiting from the multivalent boronic acid-glucose interaction and the cooperation of thiourea units, the copolymer exhibited good selectivity for glucose detection against the coexisting saccharides and other biological molecules in saliva. The nanopores with well-demonstrated analytical performance were finally applied for monitoring glucose in saliva. Together, this work unveiled a new platform for glucose detection in saliva, and promised to provide a new strategy for detecting other biomolecules in accessible biofluid involved in physiological and pathological events.

A selective probe based on 3‑aminophenyl boronic acid assembly on dithiobis(succinimidylpropionate) functionalized gold nanoparticles for sialic acid detection in human serum

Sialic acid (SA) is a notable tumor marker in human. Its increased level beyond the normal concentration in human biological samples is related to different kinds of cancers development. In this contribution, a novel colorimetric assay is reported for SA detection in form of N-acetylneuraminic acid. The sensitive detection strategy is proposed via the specific SA induced aggregation of 3‑aminophenyl boronic acid (3APBA) assembled on dithiobis(succinimidylpropionate) functionalized gold nanoparticles (AuNPs-DSP). DSP was functionalized on AuNPs through a strong AuS interaction and 3APBA was assembled on AuNPs-DSP by the amine coupling reaction between the carboxyl group of DSP on gold nanoparticles surface and the amino group of 3APBA to generate a covalent amide bond. The addition of 3APBA to buffered AuNPs-DSP generated a ruby red colloidal nanosensor. With increasing concentration of SA, a probe color turned rapidly from red to blue-gray via aggregation of AuNPs-DSP-3APBA. At optimal conditions, the absorbance ratio (A700/A520) was linear with SA concentrations ranging from 0.08 to 0.25 mM and 0.30–0.70 mM. A limit of detection of 35.0 μM was achieved which is the lowest amongst reported colorimetric methods for SA determination. The practical efficacy of the assay was demonstrated on human serum, along with no interfering effects and satisfactory accuracy and precision.

Transmission mechanism and quantum interference in fused thienoacenes coupling to Au electrodes through the thiophene rings.

So far, quantum interference in molecular devices where the anchors are inseparable parts of the whole molecule has been seldom discussed. In this article, we perform first-principles calculations on the electronic transmission properties of a series of Au-thienoacene-Au junctions where the molecule interacts with electrodes through the S atoms in thiophene rings in a fused-ring system. The calculated binding energy of the Au-S interaction is highly dependent on the substitution sites of the thiophene rings, which agrees with the experimental report that the Au-S interaction is too weak to form a junction for some molecules. The electronic coupling at the molecule-electrode contact is also affected by the molecular structure. To distinguish the coupling mechanism, we show the importance of investigating the electron distribution of frontier molecular orbitals in combination with the percentage of the π system in the partial density of states on the S atoms. Because of the difference in electronic coupling, comparison between molecules should be done with care. On the other hand, conductance suppression due to the destructive quantum interference originating from the molecular topology is demonstrated by comparing the properties of isomers with similar molecule-electrode coupling.

Ultrasensitive impedimetric mercury(II) sensor based on thymine-Hg(II)-thymine interaction and subsequent disintegration of multiple sandwich-structured DNA chains.

An impedimetric method is described for ultrasensitive analysis of mercury(II). It is based on thymine-Hg(II)-thymine interaction which causes the disintegration of multiple-sandwich structured DNA chains. DNA strands were selected that are partially complementary to the T-rich Hg(II)-specific oligonucleotides (MSO). They were immobilized on a gold electrode via Au-S interaction. Next, the MSO and the bridging strands (BS) that can connect adjacent MSOs were alternately attached through layer-by-layer hybridization. Thus, a multiple-sandwich structured interface in created that carries numerous MSOs. This leads to a change-transfer resistance (Rct) values of the electrode-electrolyte interface at faradic electrochemical impedance spectroscopy measurements in the presence of the hexacyanoferrate(II)/(III) redox probe at 0.2V (vs. Ag/AgCl). If Hg(II) is added to the solution, the MSOs selectively interact with Hg(II) to produce T-Hg(II)-T structures. Hence, the multiple-sandwich hybridization chains become disintegrated, and this causes a decrease in resistivity. The effect can be used to quantify Hg(II) over an analytical range that extends over four orders of magnitude (1 fM to 10 pM), and it has a 0.16 fM limit of detection under optimal conditions. Graphical abstract An electrochemical sensor for femtomolar level detection of Hg2+ is realized on the basis of thymine-Hg2+-thymine interaction which causes disintegration of multiple sandwich DNA hybridization strands.

Curcumin-lipoic acid conjugate as a promising anticancer agent on the surface of gold‑iron oxide nanocomposites: A pH-sensitive targeted drug delivery system for brain cancer theranostics

Brain tumor is a lethal, fast growing cancer and a difficult case for treatment. Receptor-mediated endocytosis has been recognized as one of the most effective methods for drug delivery to brain tissue by overcoming obstacles associated with conventional therapeutics. In this work, a targeted theranostic drug delivery system (DDS) was prepared based on gold‑iron oxide nanocomposites (Fe3O4@Au NCs). Lipoic acid-curcumin (LA-CUR) was synthesized and introduced as a novel anticancer drug, and glutathione (GSH) was exploited as the targeting ligand. Both LA-CUR and GSH were easily attached to Fe3O4@Au NCs via Au-S interaction. As a negatively charged nanocarrier, the prepared DDS showed relatively less protein adsorption. Accordingly, hemocompatibility assays (complement, platelet, and leucocyte activation) revealed its hemocompatible virtue, especially in respect of free LA-CUR. GSH functionalization led to 2-fold increase of cellular uptake in GSH receptor-positive astrocyte cells which could primarily indicate the probable ability of the DDS to bypass BBB. Cytotoxicity and apoptosis assays together showed the noticeably enhanced cytotoxicity of LA-CUR against cancerous U87MG cells (IC50=2.69μg/ml) in comparison with curcumin (IC50=21.31μg/ml); moreover, the DDS demonstrated relatively higher cytotoxicity against cancerous U87MG cells than normal astrocyte cells which was in accordance with pH sensitive mechanism of LA-CUR release. Besides, the results of in vitro magnetic resonance imaging (MRI) (relaxation rate (r2)=80.73 (s−1·mM−1)) primarily revealed that the DDS can be applied as a negative MRI contrast agent. In sum, the prepared DDS appeared to be a promising candidate for brain cancer treatment and a favorable MRI contrast agent.

Highly sensitive aptamer based on electrochemiluminescence biosensor for label-free detection of bisphenolA.

BisphenolA (BPA), a typical endocrine disruptor, is widely used as a key monomer in the packaging industry. Residual monomer can transfer from the package material to the food and thereby pose a risk to the health of the consumer, so determination of BPA migration is highly important for food safety control. In this study, a simple but sensitive electrochemiluminescence (ECL) biosensor, which combines the characteristics of high selectivity of an aptamer and high sensitivity of ECL, has been developed to detect BPA from package materials. The aptamer was immobilized on a gold electrode surface through Au-S interaction. The aptamer was then hybridized with complementary DNA (CDNA) to form double-stranded DNA (dsDNA). Ru(phen)32+ can intercalate into the grooves of dsDNA and acts as an ECL indicator; high ECL intensity can therefore be detected from the electrode surface. In the presence of BPA, which can competitively bind with the aptamer owing to their high affinity, Ru(phen)32+ is released from the electrode surface and the ECL of the system is decreased. The decreasing ECL signal has a linear relationship with BPA in the range of 0.1-100pM with a detection limit of 0.076pM. The developed biosensor has been applied to detect migration of BPA from different categories of canned drink with satisfactory results.

Colorimetric and visual determination of adenosine triphosphate using a boronic acid as the recognition element, and based on the deaggregation of gold nanoparticles

The authors describe a new kind of adenosine triphosphate (ATP) assay. It is based on the use of gold nanoparticles (AuNPs) coated with 4-mercaptophenylboronic acid (MPBA) as the recognition element for ATP. MPBA has a specific affinity for AuNPs through Au-S interaction, and three boronic acid groups undergo condensation to form a boroxine ring. This induces the aggregation of AuNPs and a visible color change from red to blue. However, in the presence of ATP, the boronic acid group of MPBA preferentially binds to the 2’, 3’-hydroxy group of ATP to form a stable boronate ester. Hence, the aggregation of AuNPs is progressively decreased as the concentration of ATP increases, and the color change is increasingly reversed. The ratio of absorbance at 520 and 683 nm increases linearly in the 8 to 100 μM ATP concentration range, with a 0.12 μM limit of detection (at an S/N ratio of 3 σ). The colorimetric assay was successfully applied to the determination of ATP in T47D breast cancer cells and in cultured cells with added anticarcinogen.

Electrochemical DNA sandwich biosensor based on enzyme amplified microRNA-21 detection and gold nanoparticles

In this work, a novel electrochemical biosensor for miRNA-21 determination, involving a sandwich hybridization assay onto gold nanoparticles modified pencil graphite electrode (PGE) and enzyme signal amplification was reported.The thiol terminated capture probe 1 (SH-P1) was immobilized on the electrode through AuS interaction. In the presence of target miRNA-21, SH-P1 hybridized with the first part of the target, however, the second part hybridizes with a biotinylated probe P2 (B-P2). Then, a streptavidin-conjugated alkaline phosphatase was immobilized by a specific binding of avidin-B-P2. The enzyme catalyzed the electro-inactive α-naphtyl phosphate to an electro-active α-naphtol. The miRNA-21 detection was achieved through the changes of α-naphtol oxidation signals observed at +0.12V vs Ag/AgCl with Differential Pulse Voltammetry.Under the optimal detection conditions, the biosensor exhibited selective and sensitive detection with a linear range from 200pM to 388nM and the detection limit was 100pM (10fmol in 100μL).

Electrochemiluminescence biosensor for ultrasensitive determination of ochratoxin A in corn samples based on aptamer and hyperbranched rolling circle amplification.

Determination of ochratoxin A (OTA) is highly important for food safety control. In this study, a signal-on electrochemiluminescence (ECL) biosensor which combined the characteristics of high efficiency of hyperbranched rolling circle amplification (HRCA) and high selectivity of aptamer was developed for OTA determination. The capture probe DNA (CDNA) was firstly immobilized on the gold electrode surface through Au-S interaction, then the OTA aptamer was modified on the electrode surface through hybridization with CDNA. Since OTA can competitively bind with the aptamer due to their high affinity, which would induce the releasing of aptamer from the electrode surface. Subsequently, the free CDNA on the electrode surface can hybridize with the padlock probe and induce HRCA reaction subsequently. Thus, the HRCA products which contained large amount of double-stranded DNA (dsDNA) fragments can be accumulated on the electrode surface. Since Ru(phen)3(2+) can intercalate into the groove of dsDNA and acts as ECL indicator, high ECL intensity can be detected from the electrode surface. The enhanced ECL intensity has a linear relationship with OTA in the range of 0.05-500 pg/mL with a correlation coefficient of 0.9957, and the limit of detection (LOD) was 0.02 pg/mL. The developed biosensor has been applied to determine OTA concentration in the corn samples with satisfied results.

A Fetomolar Level 17β-estradiol Electrochemical Aptasensor Constructed On Hierachical Dendritic Gold Modified Boron-Doped Diamond Electrode

It is of great significance to develop efficient monitoring strategies with high sensitivity and selectivity for 17β-estradiol (E2), a typical steroidal hormones endocrine disrupting chemicals, in water samples. Here reports a novel practical electrochemical impedance aptasensor for the detection of E2 effectively and fast. A unique hierachical dendritic gold microstructure is constructed on boron doped diamond (BDD) electrode surface through a double template method. The obtained dendritic Au/BDD electrode has lower background current, better electrochemical performance and higher capacity to immobilize biomolecules. E2 aptamers which can specifically binding to E2 were immobilized on the surface of the dendritic Au/BDD electrode through Au-S interaction, obtaining a newly-typed E2 aptasensor. The aptasensor performed supersensitive and specific recognition capacity towards E2. Once E2 enters into the detecting system, it reacts with aptamers and enlarges the interfacial electron transfer resistance significantly, which leads to the increment of impedance signal and realizes the quantification of E2. Results show that the constructed E2 aptasensor exihbits a wide linear range with the logarithm of concentration of E2 from 1.0×10−14 to 1.0×10−9mol/L with a femtomolar level detection limit of 5.0×10−15mol/L. High specificity is also evidenced by control experiments performed with the E2 aptasensor in a co-existing system including estriol, bisphenol A, nonyl phenol, diethyl phthalate, resorcinol and atrazine. Real water sample analysis showed the reliability and potential in practical environmental monitoring of the aptasensor. Besides, the aptasensor is easy to prepare, and the dendritic Au/BDD electrode can be a promising platform for design of other sensors.

Selection and Identification of DNA Aptamers against Okadaic Acid for Biosensing Application

This work describes the selection and identification of DNA aptamers that bind with high affinity and specificity to okadaic acid (OA), a lipophilic marine biotoxin that accumulates in shellfish. The aptamers selected using systematic evolution of ligands by exponential enrichment (SELEX) exhibited dissociation constants in the nanomolar range. The aptamer with the highest affinity was then used for the fabrication of a label-free electrochemical biosensor for okadaic acid detection. The aptamer was first immobilized on the gold electrode by a self-assembly approach through Au-S interaction. The binding of okadaic acid to the aptamer immobilized on the electrode surface induces an alteration of the aptamer conformation causing a significant decrease in the electron-transfer resistance monitored by electrochemical impedance spectroscopy. The aptasensor showed a linear range for the concentrations of OA between 100 pg/mL and 60 ng/mL with a detection limit of 70 pg/mL. The dissociation constant of okadaic acid with the aptamer immobilized on the electrode surface showed good agreement with that determined using fluorescence assay in solution. Moreover, the aptasensor did not show cross-reactivity toward toxins with structures similar to okadaic acid such as dinophysis toxin-1 and 2 (DTX-1, DTX-2). Further biosensing applications of the selected aptamers are expected to offer promising alternatives to the traditional analytical and immunological methods for OA detection.