School of Pharmacy, Fudan University, 826 Zhangheng Road, Shanghai, 201203, China.
Anal Bioanal Chem. 2014 Mar;406(7):1895-902. doi: 10.1007/s00216-013-7609-3. Epub 2014 Jan 18.
Herein, we demonstrate a novel silver nanocluster-based fluorescent system for the detection of nicotinamide adenine dinucleotide (NAD(+)), an important biological small molecule involved in a wide range of biological processes. A single-stranded dumbbell DNA probe was designed and used for the assay, which contained a nick in the stem, a poly-cytosine nucleotide loop close to 5' end as the template for the formation of highly fluorescent silver nanoclusters (Ag NCs) and another loop close to 3' end. Only in the presence of NAD(+), the probe was linked at 5' and 3' ends by Escherichia coli DNA ligase, which blocked the DNA polymerase-based extension reaction, ensuring the formation of fluorescent Ag NCs. This technique provided a logarithmic linear relationship in the range of 1 pM-500 nM with a detection limit of as low as 1 pM NAD(+), and exhibited high selectivity against its analogues, and was then successfully used for the detection of NAD(+) level in four kinds of cell homogenates. In addition, this new approach was conducted in an isothermal and homogeneous condition without the need of any thermal cycling, washing, and separation steps, making it very simple. Overall, this label-free protocol offers a promising alternative for the detection of NAD(+), taking advantage of specificity, sensitivity, cost-efficiency, and simplicity.
在此,我们展示了一种基于银纳米簇的新型荧光体系,用于检测烟酰胺腺嘌呤二核苷酸(NAD(+),这是一种参与广泛生物过程的重要生物小分子。设计了一种单链哑铃 DNA 探针用于检测,该探针在茎部有一个缺口,靠近 5' 端的多胞嘧啶核苷酸环作为形成高度荧光银纳米簇(Ag NCs)的模板,另一个环靠近 3' 端。只有在 NAD(+)存在的情况下,探针才能在 5' 和 3' 端被大肠杆菌 DNA 连接酶连接,这阻止了基于 DNA 聚合酶的延伸反应,确保了荧光 Ag NCs 的形成。该技术在 1 pM-500 nM 的范围内提供了对数线性关系,检测限低至 1 pM NAD(+),并对其类似物表现出高选择性,随后成功用于四种细胞匀浆中 NAD(+)水平的检测。此外,这种新方法在等温均相条件下进行,无需任何热循环、洗涤和分离步骤,非常简单。总的来说,这种无标记的方案提供了一种有前途的 NAD(+)检测替代方法,具有特异性、灵敏度、成本效益和简单性的优势。