利用带有荧光团的 AuNPs-DNA Walker 快速检测肝炎病毒

Biosensors Pub Date : 2024-07-29 DOI:10.3390/bios14080370
Baining Sun, Chenxiang Zheng, Dun Pan, Leer Shen, Wan Zhang, Xiaohua Chen, Yanqin Wen, Yongyong Shi
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引用次数: 0

摘要

病毒性肝炎是由各种肝炎病毒引起的一种全身性传染病,主要导致肝脏损伤。根据病因,肝炎病毒可分为甲型、乙型、丙型、丁型和戊型五种。目前,肝炎病毒的检测主要依靠酶联免疫吸附试验(ELISA)、免疫电子显微镜观察和识别病毒颗粒以及原位杂交检测组织中的病毒 DNA 等方法。然而,这些方法都有其局限性,包括灵敏度低、结果误差率高,以及隐性血清感染条件下可能出现的假阴性反应。为了解决这些难题,我们设计了一种 AuNPs-DNA walker 方法,它使用金纳米粒子(AuNPs)和互补 DNA 链,通过比色法和荧光检测来检测病毒 DNA 片段。附着在金纳米粒子上的 DNA 步行器包括一条结合了探针序列的长步行链和茎环结构链,茎环结构链的 3′端有一个修饰过的荧光分子,其中包含 DNA 酶结构域。加入病毒片段后,目标序列与探针链结合。随后,长游走链被释放出来,并不断与茎环结构链杂交。DNA 酶在 Mg2+ 的作用下发生水解裂解,将茎环结构链分解成线性单链。由于这些结构变化,溶液中的负电荷密度降低,削弱了空间斥力,迅速降低了 DNA 步行器的稳定性。这导致在加入高盐溶液后出现聚集,并伴有颜色变化。通过荧光检测可以进行病毒分型。这种创新方法可以检测 DNA/RNA 片段,对目标序列具有高度特异性,检测浓度可低至 1 nM。总之,我们的方法为检测肝炎病毒提供了一种更方便、更可靠的方法。
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Using AuNPs-DNA Walker with Fluorophores Detects the Hepatitis Virus Rapidly
Viral hepatitis is a systemic infectious diseases caused by various hepatitis viruses, primarily leading to liver damage. It is widely prevalent worldwide, with hepatitis viruses categorized into five types: hepatitis A, B, C, D, and E, based on their etiology. Currently, the detection of hepatitis viruses relies on methods such as enzyme-linked immunosorbent assay (ELISA), immunoelectron microscopy to observe and identify viral particles, and in situ hybridization to detect viral DNA in tissues. However, these methods have limitations, including low sensitivity, high error rates in results, and potential false negative reactions due to occult serum infection conditions. To address these challenges, we have designed an AuNPs-DNA walker method that uses gold nanoparticles (AuNPs) and complementary DNA strands for detecting viral DNA fragments through a colorimetric assay and fluorescence detection. The DNA walker, attached to gold nanoparticles, comprises a long walking strand with a probe sequence bound and stem-loop structural strands featuring a modified fluorescent molecule at the 3′ end, which contains the DNAzyme structural domain. Upon the addition of virus fragments, the target sequence binds to the probe chains. Subsequently, the long walking strand is released and continuously hybridizes with the stem-loop structural strand. The DNAzyme undergoes hydrolytical cleavage by Mg2+, breaking the stem-loop structural strand into linear single strands. As a result of these structural changes, the negative charge density in the solution decreases, weakening spatial repulsion and rapidly reducing the stability of the DNA walker. This leads to aggregation upon the addition of a high-salt solution, accompanied by a color change. Virus typing can be performed through fluorescence detection. The innovative method can detect DNA/RNA fragments with high specificity for the target sequence, reaching concentrations as low as 1 nM. Overall, our approach offers a more convenient and reliable method for the detection of hepatitis viruses.
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