Hong Guolin, Zou Zhiyan, Huang Zhongnan, Deng Haohua, Chen Wei, Peng Huaping
School of Clinical Medicine, Fujian Medical University, Fuzhou, 350004, China; Department of Laboratory Medicine, Xiamen Key Laboratory of Genetic Testing, The First Affiliated Hospital of Xiamen University, Xiamen, 361003, China.
School of Clinical Medicine, Fujian Medical University, Fuzhou, 350004, China; Higher Educational Key Laboratory for Nano Biomedical Technology of Fujian Province, Department of Pharmaceutical Analysis, Fujian Medical University, Fuzhou, 350004, China.
Biosens Bioelectron. 2021 Apr 15;178:113044. doi: 10.1016/j.bios.2021.113044. Epub 2021 Jan 28.
Persistent high-risk human papillomavirus (HPV) infection is the leading cause of cervical cancer. Efficient detection of HPV16 E7 is necessary for early diagnosis and cure of the disease. Here, a novel and high-performance Au nanocluster (AuNC) probe-based split-type electrochemiluminescent (ECL) assay platform has been established to detect these oncogenes, in which the nucleic acid hybridization assay and the ECL measurements are performed independently. The proposed approach combines superior magnetic nanobead enrichment and separation technology, specific nucleic acid hybridization technology, and high-efficiency AuNC probe ECL strategy, and shows excellent advantages. First, the split-type ECL sensing platform can effectively avoid interference from biological samples and adequately uses the ECL efficiency of the AuNC probe. Furthermore, the ultrahigh sensitivity assay of HPV DNA can be achieved without any complex nucleic acid amplification technique. Taking advantage of the above merits of split-type detection, the ECL DNA sensor achieved ideal low detection of 6.8 aM and a wide dynamic range bridging 10 orders of magnitude HPV16 E7. Furthermore, together with its favorable and powerful specificity, high sensitivity, and good selectivity, this strategy could detect HPV16 E7 DNA in human samples, which showed great consistency with the FDA-approved approach (Hybrid capture 2, HC2). Therefore, this work proposes a facile and reliable split-type ECL platform for HPV diagnosis and shows great potential for the early diagnosis of other diseases.
持续性高危型人乳头瘤病毒(HPV)感染是宫颈癌的主要病因。高效检测HPV16 E7对于该疾病的早期诊断和治愈至关重要。在此,已建立了一种基于新型高性能金纳米簇(AuNC)探针的分裂型电化学发光(ECL)检测平台来检测这些致癌基因,其中核酸杂交检测和ECL测量是独立进行的。所提出的方法结合了卓越的磁性纳米珠富集和分离技术、特异性核酸杂交技术以及高效的AuNC探针ECL策略,并显示出优异的优势。首先,分裂型ECL传感平台可有效避免生物样品的干扰,并充分利用AuNC探针的ECL效率。此外,无需任何复杂的核酸扩增技术即可实现HPV DNA的超高灵敏度检测。利用分裂型检测的上述优点,ECL DNA传感器实现了6.8 aM的理想低检测限以及跨越10个数量级的宽动态范围的HPV16 E7检测。此外,该策略具有良好且强大的特异性、高灵敏度和良好的选择性,能够检测人样品中的HPV16 E7 DNA,与FDA批准的方法(杂交捕获2,HC2)具有高度一致性。因此,这项工作提出了一种用于HPV诊断的简便可靠的分裂型ECL平台,并在其他疾病的早期诊断中显示出巨大潜力。