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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增强石墨化氮化碳纳米片的内在过氧化物酶样活性及其在外泌体检测中的应用

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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:本工作研究单链DNA(ssDNA)增强g-C3N4纳米片(NSs)的固有过氧化物酶样活性的能力。我们发现,吸附在g-C3N4 NSs上的ssDNA可以提高纳米片的催化活性。 ssDNA-NSs杂合体催化H2O2介导的TMB氧化的最大反应速率比未修饰的NSs快至少4倍。活性的增强可以归因于TMB和ssDNA之间的强相互作用,其通过静电吸引和芳族堆积以及ssDNA的长度和碱基组成两者介导。如果在杂交构建中使用针对外泌体的表面标志物CD63的适体,则ssDNA-NSs杂交体的高催化活性允许对外泌体进行灵敏的比色检测。该传感器识别出乳腺癌细胞系(MCF-7)和对照细胞系(MCF-10A)产生的外泌体之间CD63的差异表达。而且,在从乳腺癌患者和健康对照者收集的血清样品中分离出的循环外来体中检测到类似的趋势。我们的工作揭示了使用ssDNA增强纳米材料的过氧化物酶样活性的可能性,并证明了ssDNA-NSs杂交体在液体活检临床诊断中的巨大潜力。

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