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首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Colorimetric assay for protein detection based on 'nano-pumpkin' induced aggregation of peptide-decorated gold nanoparticles
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Colorimetric assay for protein detection based on 'nano-pumpkin' induced aggregation of peptide-decorated gold nanoparticles

机译:基于“纳米南瓜”诱导的肽修饰金纳米颗粒聚集的比色法检测蛋白质

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摘要

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.
机译:小肽可用作有效的生物识别元件,并提供蛋白质检测的替代工具。然而,由于信号转导的困难,基于肽的检测策略的发展仍然难以捉摸。在本文中,我们以血管内皮生长因子受体1(Flt-1)为例,报道了一种基于肽的比色法来检测疾病的生物标志物。在此策略中,通过引入葫芦[8] uril(CB [8])可以选择性地同时容纳两个肽的N端芳香族残基,从而使含N端芳香族残基的肽修饰的金纳米颗粒(GNP)形成庞大的聚集体。不论顺序如何。但是,在Flt-1存在的情况下,该肽可以与蛋白质分子特异性结合,并且N末端的芳香族残基将被占据,从而导致GNP很少聚集。通过利用高亲和力肽和CB [8]与GNP的高效交联作用,可以以0.2 nM的检出限进行蛋白质检测的量热法,与传统方法相当。我们的方法的可行性也已经在加标血清样品中得到了证明,表明了将来的潜在应用。 (C)2015 Elsevier B.V.保留所有权利。

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