跳至主要内容

Design of electrochemical biosensors with peptide probes as the receptors of targets and the inducers of gold nanoparticles assembly on electrode surface

文献作者:Ning Xia, Xin Wang, Jie Yu, Yangyang Wu, Shuchao Cheng, Yun Xing, Lin Liu   《Sensors and Actuators B: Chemical》


ABSTRACTS
We reported a general way to design electrochemical biosensors with peptide probes as the receptors of targets and the inducers of gold nanoparticles (AuNPs) assembly on electrode surface. To demonstrate the feasibility of our strategy, human chorionic gonadotropin (hCG) was first determined as a model analyte. Specifically, the hCG-binding peptide triggered the aggregation of AuNPs in solution; by modifying the electrode with the hCG-binding peptide, the peptide-induced AuNPs assembly was achieved on the electrode surface, resulting in the formation of a network of AuNPs and a significant fall of charge transfer resistance. The attachment of hCG onto the electrode surface through the probe-target interaction made the peptide lose its ability to trigger the formation of the AuNPs-based network architecture on electrode surface, thus leading to an increased charge transfer resistance. The electrochemical impedance technique allowed for the determination of hCG with a detection limit 0.6 mIU/mL. Furthermore, the method was used to the selective detection of amyloid-β oligomer (AβO, a reliable molecular biomarker and crucial target for the diagnosis and therapeutic intervention of Alzheimer's disease). Our result indicated that the AuNPs-based colorimetric assay can be developed into a corresponding electrochemical assay with significantly improving sensitivity and selectivity. Taking advantage of the simple principle and the unique physical and chemical properties of AuNPs, our work would be valuable for the design of novel electrochemical biosensors by marrying specific receptors.
KEY WORDS
Electrochemical biosensor; Human chorionic gonadotropin; Amyloid-β; Peptide aptamer; Gold nanoparticles; Colorimetric assay.
SCREENSHOT

RELATED PRODUCTS
Peptides used in this work were synthesized and purified by China Peptides Co., Ltd. (Shanghai, China) .
CHAINING
https://www.sciencedirect.com/science/article/pii/S0925400516313120

评论

此博客中的热门博文

The therapeutic effect of anti-CD52 treatment in murine experimental autoimmune encephalomyelitis is associated with altered IL-33 and ST2 expression levels

文献作者:Mark Barbour, Rachel Wood, Shehla U.Hridi, Chelsey Wilson, Grant McKay, Trevor J.Bushell, Hui-Rong Jiang   《Journal of Neuroimmunology》 ABSTRACTS Experimental autoimmune encephalomyelitis  (EAE) mice were administered with murine anti-CD52  antibody  to investigate its therapeutic effect and whether the treatment modulates IL-33 and ST2 expression. EAE severity and  central nervous system  (CNS) inflammation were reduced following the treatment, which was accompanied by peripheral  T and B lymphocyte  depletion and reduced production of various  cytokines  including IL-33, while sST2 was increased. In spinal cords of EAE mice, while the number of IL-33 +  cells remained unchanged, the extracellular level of IL-33 protein was significantly reduced in anti-CD52 antibody treated mice compared with controls. Furthermore the number of ST2 +  cells in the spinal cord of treated EAE mice was  downregulated ...

Mutational analysis of the extracellular disulphide bridges of the atypical chemokine receptor ACKR3/CXCR7 uncovers multiple binding and activation modes for its chemokine and endogenous non-chemokine agonists

Author:Martyna Szpakowska, Max Meyrath, Nathan Reynders,  Manuel Counson, Julien Hanson, Jan Steyaert, Andy Chevigné     《Biochemical Pharmacology》 ABSTRACTS The atypical chemokine receptor ACKR3/CXCR7 plays crucial roles in numerous physiological processes but also in viral infection and cancer. ACKR3 shows strong propensity for activation and, unlike classical chemokine receptors, can respond to chemokines from both the CXC and CC families as well as to the endogenous peptides BAM22 and adrenomedullin. Moreover, despite belonging to the G protein coupled receptor family, its function appears to be mainly dependent on β-arrestin. ACKR3 has also been shown to continuously cycle between the plasma membrane and the endosomal compartments, suggesting a possible role as a scavenging receptor. So far, the molecular basis accounting for these atypical binding and signalling properties remains elusive. Noteworthy, ACKR3 extracellular domains bear three  di...

CAS:85466-18-8|Thymopoietin II (32-35)|RKDV

Contact: Liven Qian(钱叶华)-Custom Peptide Mobile: 13761298676(微信) Email:cps037@chinapeptides.net QQ:2880526724 ChinaPeptides Co., Ltd./强耀生物科技有限公司 Name Thymopoietin II (32-35) Code [85466-18-8] The alias Thymopoietin II (32-35) Sequence (single letter abbreviation) RKDV Sequence (three-letter abbreviation) H-Arg-Lys-Asp-Val-OH (trifluoroacetate salt) A basic description TP-4 and TP-3; shortest active thymopoietin II fragments described that exhibit potent immunoregulatory properties in vitro and in vivo. solubility The molecular weight 516.6 Chemical formula C21H40N8O7 The purity 80%,90%,95%,98%,99% Weight 1mg,5mg,10mg,50mg,100mg,1g Storage conditions Store at -20°C. Keep tightly closed. Store in a cool dry place. Number of Residues: 4 1-Letter Code: RKDV 3-Letter Code: Arg-Lys-Asp-Val Molecular weight (Mr): 516.6 g/mol Isoelectric point: 10.1 Net charge at pH 7.0: 1.0 Average hydrophilicity: 1.9 Ratio of hydrophilic residues / total number of residues...