School of Chemistry and Astbury Centre for Structural Molecular Biology, University of Leeds , Leeds LS2 9JT, U.K.
Anal Chem. 2013 Oct 1;85(19):9238-44. doi: 10.1021/ac402081u. Epub 2013 Sep 12.
We report herein the development of a simple, sensitive colorimetric magnetic nanoparticle (MNP)-enzyme-based DNA sandwich assay that is suitable for simultaneous, label-free quantitation of two DNA targets down to 50 fM level. It can also effectively discriminate single-nucleotide polymorphisms (SNPs) in genes associated with human cancers (KRAS codon 12/13 SNPs). This assay uses a pair of specific DNA probes, one being covalently conjugated to an MNP for target capture and the other being linked to an enzyme for signal amplification, to sandwich a DNA target, allowing for convenient magnetic separation and subsequent efficient enzymatic signal amplification for high sensitivity. Careful optimization of the MNP surfaces and assay conditions greatly reduced the background, allowing for sensitive, specific detection of as little as 5 amol (50 fM in 100 μL) of target DNA. Moreover, this sensor is robust, it can effectively discriminate cancer-specific SNPs against the wild-type noncancer target, and it works efficiently in 10% human serum. Furthermore, this sensor can simultaneously quantitate two different DNA targets by using two pairs of unique capture- and signal-DNA probes specific for each target. This general, simple, and sensitive DNA sensor appears to be well-suited for a wide range of genetics-based biosensing and diagnostic applications.
我们在此报告了一种简单、灵敏的比色磁纳米粒子(MNP)-酶基 DNA 夹心测定法的发展,该方法适用于同时、无标记地定量检测两种 DNA 靶标,检测下限可达 50 fM 水平。它还可以有效地鉴别与人类癌症相关基因中的单核苷酸多态性(SNP)(KRAS 密码子 12/13 SNP)。该测定法使用一对特定的 DNA 探针,一个通过共价键连接到 MNP 上用于靶标捕获,另一个连接到酶上用于信号放大,夹在 DNA 靶标上,允许方便地进行磁分离,随后进行高效的酶信号放大,从而实现高灵敏度。仔细优化 MNP 表面和测定条件大大降低了背景,从而能够灵敏、特异地检测低至 5 amol(100 μL 中 50 fM)的目标 DNA。此外,该传感器具有鲁棒性,能够有效地鉴别针对野生型非癌靶标的癌症特异性 SNP,并且在 10%的人血清中也能有效工作。此外,该传感器可以通过使用两对针对每个靶标特异的独特捕获和信号 DNA 探针同时定量两种不同的 DNA 靶标。这种通用、简单、灵敏的 DNA 传感器似乎非常适合广泛的基于遗传学的生物传感和诊断应用。