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基于氨基修饰磁性纳米粒子的用于 PCR 分析的 DNA 提取方法。

A method based on amino-modified magnetic nanoparticles to extract DNA for PCR-based analysis.

机构信息

Institute for Agro-food Standards and Testing Technology, Laboratory of Quality & Safety Risk Assessment for Agro-products (Shanghai), Ministry of Agriculture, Shanghai Academy of Agricultural Sciences, Shanghai, 201403, China.

Department of Chemistry, University of Minnesota, Minneapolis, MN, 55455, United States.

出版信息

Colloids Surf B Biointerfaces. 2019 Jul 1;179:87-93. doi: 10.1016/j.colsurfb.2019.03.005. Epub 2019 Mar 6.

Abstract

DNA extraction using magnetic particles (MPs) is a simple and rapid process. MPs directly combine with DNA, thereby facilitating removal of impurities in complex samples by magnetic attraction. Amino-modified magnetic nanoparticles (AMNPs) have been described as poor substrates for DNA extraction because it was difficult to desorb DNA from the AMNPs for downstream assays. In this study, we proposed to use the complexes of AMNPs and DNA directly as templates for PCR, thereby bypassing the difficulty of desorbing DNA from AMNPs. At first, we compared three distinct chemical modifications for magnetic nanoparticles (hydroxyl modified-, carboxyl modified-, and amino modified-magnetic nanoparticles) for the extraction of DNA under experimental conditions compatible with downstream assays (e.g., PCR). Under such conditions, we demonstrated that only the AMNPs had a powerful adsorption capability for DNA with 98% separation rate. We directly employed the complexes of AMNPs and extracted DNA as templates for PCR, which reduced the separation steps and minimized the loss of DNA. Notably, we minimized AMNPs-caused inhibition of the PCR by adding BSA to the PCR mixture. The AMNPs extraction was successfully applied for the detection of a genetically modified organism, species identification, and an allergen in a heterogenous mixture. The AMNPs-based extraction method is a simple and rapid process to extract DNA and even trace amounts of DNA for PCR-based analysis.

摘要

采用磁性粒子 (MPs) 提取 DNA 是一种简单、快速的方法。MPs 可直接与 DNA 结合,从而通过磁吸引作用去除复杂样品中的杂质。氨基修饰的磁性纳米粒子 (AMNPs) 被描述为提取 DNA 的较差基质,因为难以将 DNA 从 AMNPs 上解吸下来用于下游分析。在这项研究中,我们建议直接将 AMNPs 和 DNA 的复合物用作 PCR 的模板,从而绕过从 AMNPs 上解吸 DNA 的困难。首先,我们比较了三种不同的化学修饰的磁性纳米粒子(羟基修饰的、羧基修饰的和氨基修饰的磁性纳米粒子)在与下游分析(例如 PCR)兼容的实验条件下提取 DNA 的效果。在这种条件下,我们证明只有 AMNPs 对 DNA 具有强大的吸附能力,分离率达到 98%。我们直接将 AMNPs 和提取的 DNA 的复合物用作 PCR 的模板,减少了分离步骤,最大限度地减少了 DNA 的损失。值得注意的是,我们通过在 PCR 混合物中添加 BSA 来最小化 AMNPs 对 PCR 的抑制作用。该 AMNPs 提取方法成功应用于检测转基因生物、物种鉴定和异质混合物中的过敏原。基于 AMNPs 的提取方法是一种简单、快速的提取 DNA 的方法,甚至可以提取痕量 DNA 用于基于 PCR 的分析。

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