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一种基于反向剪接连接检测肝细胞癌环状RNA的无PCR丝网印刷磁性电极。

A PCR-free screen-printed magnetic electrode for the detection of circular RNA from hepatocellular cancer based on a back-splice junction.

作者信息

Zhang Bin, Liang Yitao, Bo Liang, Chen Mingyu, Huang Bobo, Cao Qingpeng, Wei Jinwei, Li Tianyu, Cai Xiujun, Ye Xuesong

机构信息

Biosensor National Special Laboratory, Key Laboratory of Biomedical Engineering of Ministry of Education, College of Biomedical Engineering and Instrument Science, Innovation Centre for Minimally Invasive Technique and Device, Zhejiang University Hangzhou 310027 PR China

Department of General Surgery, Sir Run Run Shaw Hospital, School of Medicine, Zhejiang University 3 East Qingchun Road Hangzhou 310016 PR China

出版信息

RSC Adv. 2021 May 17;11(29):17769-17774. doi: 10.1039/d1ra01033f. eCollection 2021 May 13.

Abstract

Circular RNA (circRNA) has the potential to be applied to disease diagnosis and therapy. However, the currently available circRNA detection techniques are limited. This work proposes a sensitive and selective approach for circRNA detection based on gold nanoparticle-modified screen-printed magnetic electrodes (AuNPs-SPME). Magnetic beads (MBs) with capture probes based on specific back-splice junction (BSJ) sites were employed to identify and selectively isolate the target circRNA, which could be directly adsorbed onto the AuNPs-SPME. Then, the circRNA attached to the surface was detected by changes in the methylene blue redox signal. The simple and time-saving AuNPs-SPME is highly sensitive (LOD = 1.0 pM) to circCDYL, one of the biomarkers of hepatocellular cancer (HCC). The analytical performance of the method presented has also been verified in human serum samples, holding great promise for clinical diagnosis.

摘要

环状RNA(circRNA)有潜力应用于疾病诊断和治疗。然而,目前可用的circRNA检测技术有限。这项工作提出了一种基于金纳米颗粒修饰的丝网印刷磁电极(AuNPs-SPME)的灵敏且选择性的circRNA检测方法。使用带有基于特定反向剪接连接(BSJ)位点的捕获探针的磁珠(MBs)来识别并选择性分离目标circRNA,该circRNA可直接吸附到AuNPs-SPME上。然后,通过亚甲基蓝氧化还原信号的变化来检测附着在表面的circRNA。这种简单省时的AuNPs-SPME对circCDYL(肝细胞癌(HCC)的生物标志物之一)具有高度敏感性(检测限 = 1.0 pM)。所提出方法的分析性能也已在人血清样本中得到验证,在临床诊断方面极具前景。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/94d4/9033221/ea3623d7a97e/d1ra01033f-s1.jpg

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