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通过滚环扩增和磁性粒子介导的聚集实现核酸的肉眼检测。

Naked-eye detection of nucleic acids through rolling circle amplification and magnetic particle mediated aggregation.

机构信息

Institute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou 310058, China.

出版信息

Biosens Bioelectron. 2013 Sep 15;47:515-9. doi: 10.1016/j.bios.2013.03.056. Epub 2013 Apr 6.

Abstract

We are presenting a new method for sequence-specific and naked-eye detection of nucleic acids (NAs) through isothermal amplification and magnetic particle mediated aggregation. A padlock probe was designed to hybridize to specific sequence on target genes followed by ligation and rolling circle amplification (RCA). Magnetic particles (MPs) were then added into RCA products solution. MPs would physically combine with long linear DNA coils (such as products of RCA reaction) and form visible intertwined aggregates, while no aggregate was observed in the absence of high molecular weight NAs (>1kb). As little as 0.62amol (124fM) of target DNA molecules was detected by the naked eye. It was further applied to detect human papillomavirus type 18 gene in genomic DNA isolated from HeLa cells. This assay is sensitive and low-cost with minimal instrumentation, revealing great potential for molecular diagnostics in developing countries and regions with limited settings.

摘要

我们提出了一种新的方法,通过等温扩增和磁颗粒介导的聚集来实现核酸(NA)的序列特异性和肉眼检测。设计了一种发夹探针与靶基因上的特定序列杂交,然后进行连接和滚环扩增(RCA)。然后将磁珠(MPs)加入到 RCA 产物溶液中。 MPs 将与长线性 DNA 线圈(如 RCA 反应产物)物理结合并形成可见的交织聚集物,而在没有高分子质量 NA(>1kb)的情况下则没有观察到聚集物。通过肉眼检测到低至 0.62amol(124fM)的目标 DNA 分子。进一步将其应用于检测来自 HeLa 细胞的基因组 DNA 中的人乳头瘤病毒 18 基因。该检测方法具有较高的灵敏度和低成本,所需仪器设备较少,为发展中国家和仪器设备有限的地区的分子诊断提供了巨大的潜力。

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