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基于阳离子肽修饰血红素/G-四链体增强过氧化物酶样活性的新型电化学生物传感器。

Novel electrochemical biosensor based on cationic peptide modified hemin/G-quadruples enhanced peroxidase-like activity.

机构信息

College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450001, PR China.

College of Chemistry and Molecular Engineering, Zhengzhou University, Zhengzhou 450001, PR China.

出版信息

Biosens Bioelectron. 2018 Jun 1;107:178-183. doi: 10.1016/j.bios.2018.02.014. Epub 2018 Feb 9.

Abstract

This work designed an artificial substrate peptide to synthesize peptide-hemin/G-quadruplex (peptide-DNAzyme) conjugates. In addition to enhancing catalytic activity of hemin/G-quadruplex, the peptide could also be induced and cleaved by prostate specific antigen (PSA). It was the first report on peptide-DNAzyme conjugates in application of the peptide biosensor. The polyethyleneimine-reduced graphene oxide@hollow platinum nanotubes (PEI-rGO@PtNTs) nanocomposites were cast on the glassy carbon electrode in order to form the interface of biocompatibility and huge surface area for bioprobes immobilization. In absence of PSA, the peptide-DNAzyme conjugates retained intact on the surface of the electrode to produce a strong response signal. But in presence of PSA, the peptide-DNAzyme conjugates were destroyed to release electron mediators, resulting in dramatical decrease of the electrochemicl signal. Therefore, the method had high sensitivity and super selectivity with the limit of detection calculated as 2.0 fg/mL. Furthermore, the strategy would be promising to apply for other proteases by transforming the synthetic peptide module of target.

摘要

这项工作设计了一种人工基质肽来合成肽-血红素/G-四链体(肽-DNA 酶)缀合物。除了增强血红素/G-四链体的催化活性外,该肽还可以被前列腺特异性抗原(PSA)诱导和切割。这是肽-DNA 酶缀合物在肽生物传感器应用中的首次报道。将聚乙烯亚胺还原氧化石墨烯@中空铂纳米管(PEI-rGO@PtNTs)纳米复合材料浇铸在玻碳电极上,以形成生物探针固定的生物相容性和巨大表面积的界面。在没有 PSA 的情况下,肽-DNA 酶缀合物在电极表面保持完整,产生强烈的响应信号。但是在 PSA 存在的情况下,肽-DNA 酶缀合物被破坏以释放电子介体,导致电化学信号急剧下降。因此,该方法具有高灵敏度和超选择性,检测限计算为 2.0 fg/mL。此外,通过转换目标的合成肽模块,该策略有望应用于其他蛋白酶。

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