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首页> 外文期刊>Analytical chemistry >Enhancement of the Intrinsic Peroxidase-Like Activity of Graphitic Carbon Nitride Nanosheets by ssDNAs and Its Application for Detection of Exosomes
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Enhancement of the Intrinsic Peroxidase-Like Activity of Graphitic Carbon Nitride Nanosheets by ssDNAs and Its Application for Detection of Exosomes

机译:SSDNA的石墨氮化物纳米液的固有过氧化物酶样活性的增强及其检测外泌体的应用

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摘要

The present work investigates the capability of single-stranded DNA (ssDNA) in enhancing the intrinsic peroxidase-like activity of the g-C3N4 nanosheets (NSs). We found that ssDNA adsorbed on g-C3N4 NSs could improve the catalytic activity of the nanosheets. The maximum reaction rate of the H2O2-mediated TMB oxidation catalyzed by the ssDNA-NSs hybrid was at least 4 times faster than that obtained with unmodified NSs. The activity enhancement could be attributed to the strong interaction between TMB and ssDNA mediated by electrostatic attraction and aromatic stacking and by both the length and base composition of the ssDNA. The high catalytic activity of the ssDNA-NSs hybrid permitted sensitive colorimetric detection of exosomes if the aptamer against CD63, a surface marker of exosome, was employed in hybrid construction. The sensor recognized the differential expression of CD63 between the exosomes produced by a breast cancer cell line (MCF-7) and a control cell line (MCF-10A). Moreover, a similar trend was detected in the circulating exosomes isolated from the sera samples collected from breast cancer patients and healthy controls. Our work sheds lights on the possibility of using ssDNA to enhance the peroxidase-like activity of nanomaterials and demonstrates the high potential of the ssDNA-NSs hybrid in clinical diagnosis using liquid biopsy.]]>
机译:<![cdata [ src ='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/ancham/2017/chatham.2017.89.issue-22/acs.analchem.7b03335/ 20171115 /图像/介质/ ac-2017-03335Y_0008.gif“>目前的工作调查了单链DNA(SSDNA)在增强GC 3 n 4 nanosheets(nss)。我们发现吸附在G-C 3 n 4 nss上的ssdna可以改善纳米蛋白酶的催化活性。由SSDNA-NSS杂种催化的H 2 O 2 介导的TMB氧化的最大反应速率比用未修饰的NSS获得的速度快4倍。活性增强可归因于静电吸引和芳族堆叠介导的TMB和SSDNA之间的强相互作用以及SSDNA的长度和基础组成。如果采用杂交结构,则SSDNA-NSS杂交的高催化活性呼吸敏感性敏感的比例检测外来的Aptamer。杂交施工。传感器识别由乳腺癌细胞系(MCF-7)和对照细胞系(MCF-10A)产生的外泌体之间CD63的差异表达。此外,在从乳腺癌患者和健康对照中收集的血清样本中分离的循环外来检测到类似的趋势。我们的工作揭示了使用SSDNA来增强纳米材料的过氧化物酶样活性的可能性,并在临床诊断中使用液体活组织检查显示SSDNA-NSS杂种的高潜力。]]]>

著录项

  • 来源
    《Analytical chemistry》 |2017年第22期|共7页
  • 作者单位

    Institute of Chemical Biology and Nanomedicine State Key Laboratory of Chemo/Bio-Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha Hunan 410082 P. R. China;

    Institute of Chemical Biology and Nanomedicine State Key Laboratory of Chemo/Bio-Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha Hunan 410082 P. R. China;

    Department of Chemistry University of California at Riverside Riverside California 92521 United States;

    Department of Chemistry University of California at Riverside Riverside California 92521 United States;

    Department of Chemistry University of California at Riverside Riverside California 92521 United States;

    Institute of Chemical Biology and Nanomedicine State Key Laboratory of Chemo/Bio-Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha Hunan 410082 P. R. China;

    Institute of Chemical Biology and Nanomedicine State Key Laboratory of Chemo/Bio-Sensing and Chemometrics College of Chemistry and Chemical Engineering Hunan University Changsha Hunan 410082 P. R. China;

    Department of Chemistry University of California at Riverside Riverside California 92521 United States;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 分析化学;
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