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Taking advantages of the toehold-triggered strand displacement reaction (TSDR) and host-guest interaction of β-cyclodextrin (β-CD), a facile enzyme-free and homogeneous electrochemical sensing strategy was designed for the sensitive assay of target DNA using Fe 3 O 4 @SiO 2 @β-CD nanocomposites and ferrocene-labeled hairpin DNA (H-1) as the capture and electrochemical probes, respectively. Upon addition of target molecule, the initiated TSDR process induced the conformational change of H-1, and subsequently stimulated the dynamic assembly of assist probes (A-1 and A-2) to generate H-1:A-1:A-2 duplex along with the release of target sequence. The released target could drive the next TSDR recycling and finally result in the formation of numerous DNA duplex. After the molecular recognition of Fe 3 O 4 @SiO 2 @β-CD nanocomposites, a large number of duplex were easily separated from the supernatant solution under an external magnetic field, which led to a decreased H-1 concentration in residual solution, concomitant with a remarkable reduction of peak current. Under the optimized conditions, wide linear range (1–5000 pM), low detection limit (0.3 pM), desirable reproducibility, good selectivity, and satisfactory practical analysis were obtained by the combination of the superior recognition capability of β-CD, TSDR-induced signal amplification, and homogeneous electroanalytical method. The proposed detection strategy could offer a universal approach for the monitoring of various biological analytes via the rational design of probe sequences. [ABSTRACT FROM AUTHOR]

Abstract: Biofunctionalized graphene-gold nanoparticle (AuNP) hybrids were prepared using a facile approach of in situ growth, with homogeneous distribution of AuNPs on the graphene nanosheets. Hemoglobin (Hb) was immobilized on the graphene-AuNP composites to fabricate biosensors for determination of nitrite (NO2 −). A pair of well-defined redox peaks was observed for Hb immobilized on the graphene-AuNP hybrids with a formal potential (E 0′) of −0.314V in 0.1M phosphate buffered saline (0.15M NaCl, pH 7.0). The novel biosensors exhibited many advantages, such as wide linear response range (from 0.05 to 1000µM, R 2=0.997), low detection limit (0.01µM, a signal to noise ratio of 3), high sensitivity (0.15μAμM−1 cm−2), and excellent selectivity. These constructed biosensors were further used for determination of nitrite in pickled radish. The results obtained were in good agreement with those using spectrophotometry based on the National Food Safety Standard (GB 5009.33-2010), which indicates that these novel and sensitive biosensors have promising application for determination of nitrite in food. [Copyright &y& Elsevier]

Nowadays, acquired immunodeficiency syndrome has become a formidable danger to human health, and its early diagnosis is urgent need with the increasing quantity of patients around the world. Herein, we first synthesized beta-cyclodextrin-functionalized CdS nanorods (β-CD@CdS NRs) with high stability and desirable photo-electricity activity, and served as easy-to-assemble building modules to design a novel photoelectrochemical biosensor for human immune deficiency virus (HIV) DNA detection by coupling with catalytic hairpin assembly (CHA)-mediated biocatalytic precipitation and the host-guest interaction between adamantine (ADA) and β-CD. In the presence of HIV DNA, CHA process was triggered with the aid of hairpin DNA1 and ADA-labelled hairpin DNA2, and then generated large amounts of G-quadruplex, which could be formed hemin/G-quadruplex DNAzyme to catalyze 4-chloro-1-naphthol to generate insoluble precipitation on photoelectrode surface, followed by the decreased photocurrent response due to the corresponding stereo-hindrance effect. Under optimized conditions, this biosensor exhibited wide linear dynamic range (10 fM – 1 nM) and low detection limit of 1.16 fM, as well as high sensitivity, excellent stability, and satisfactory feasibility in human-serum samples. Moreover, the prepared β-CD@CdS NRs could be applied to the construction of other advanced sensing platform, showing great prospect in clinical diagnostics. • Easy-to-assemble and stable β-CD@CdS NRs were firstly fabricated. • β-CD@CdS NRs as building modules were utilized to the photoelectrochemical bioassay of HIV DNA. • High sensitivity and low detection limit stemmed from the introduction of CHA process and β-CD@CdS NRs. • The biosensor achieved extensive prospect in real human serum sample detection. [ABSTRACT FROM AUTHOR]