4.8 Article

Colorimetric assay for protein detection based on nano-pumpkin induced aggregation of peptide-decorated gold nanoparticles

Journal

BIOSENSORS & BIOELECTRONICS
Volume 71, Issue -, Pages 348-352

Publisher

ELSEVIER ADVANCED TECHNOLOGY
DOI: 10.1016/j.bios.2015.04.072

Keywords

Cucurbit[8]Uril; Gold nanoparticle; Peptide; Protein detection

Funding

  1. National Natural Science Foundation of China [21235003]
  2. National Science Fund for Distinguished Young Scholars [20925520]

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Small peptide can be used as an effective biological recognition element and provide an alternative tool for protein detection. However, the development of peptide-based detecting strategy still remains elusive due to the difficulty of signal transduction. Herein, we report a peptide-based colorimetric strategy for the detection of disease biomarker by using vascular endothelial growth factor receptor 1 (Flt-1) as an example. In this strategy, N-terminal aromatic residue-containing peptide modified gold nanoparticles (GNPs) can form bulky aggregate by the introduction of cucurbit[8]uril (CB[8]) that can selectively accommodate two N-terminal aromatic residue of peptides simultaneously regardless of their sequences. However, in the presence of Flt-1, the peptide can specifically bind to the protein molecule and the N-terminal aromatic residue will be occupied, resulting in little aggregation of GNPs. By taking advantage of the highly affinitive peptide and efficiency cross-linking effect of CB[8] to GNPs, calorimetric assay for protein detection can be achieved with a detection limit of 0.2 nM, which is comparable with traditional methods. The feasibility of our method has also been demonstrated in spiked serum sample, indicating potential application in the future. (C) 2015 Elsevier B.V. All rights reserved.

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