Gao Lingfeng, He Xiao, Ju Li, Liu Xiaoying, Li Fang, Cui Hua
CAS Key Laboratory of Soft Matter Chemistry, Collaborative Innovation Center of Chemistry for Energy Materials, Department of Chemistry, University of Science and Technology of China, Jinzhai Road 96, Hefei, Anhui, 230026, China.
Anal Bioanal Chem. 2016 Dec;408(30):8747-8754. doi: 10.1007/s00216-015-9244-7. Epub 2016 Jan 11.
Sensitive, specific, simple, fast, and low-cost DNA detection methods are extremely important in clinical diagnostics, gene therapy, and a variety of biomedical studies. In this work, we developed a general method for the detection of specific DNA sequences from Mycobacterium tuberculosis (TB), hepatitis B virus (HBV), and myelocytomatosis viral oncogene (v-myc) using gold nanoparticles bifunctionalized with both a chemiluminescent (CL) reagent and a catalytic metal complex as signal reporters and a DNA strand complementary to the target as the capture probe. In this CL method, a biotinylated single-strand DNA capture probe was immobilized in a streptavidin-coated microwell. Upon the addition of the target single-strand DNA, the capture probe hybridized with the target DNA. After adding the bifunctionalized gold nanoparticles and HO, a well-defined CL signal was obtained, and the CL intensity was observed to change as the target DNA concentration was increased. It was possible to determine the concentration of the target TB single-strand DNA in the range 1.0 × 10-1.0 × 10 M with a detection limit of 4.8 × 10 M. HBV single-strand DNA and v-myc single-strand DNA could also be determined in the range 1.0 × 10-1.0 × 10 M with detection limits of 5.9 × 10 M and 8.0 × 10 M, respectively, using this CL technique. The method reported in this paper is the first label-free CL method for the determination of specific DNA sequences to utilize gold nanoparticles bifunctionalized with both a CL reagent and a catalytic metal complex. The sensitivity of this CL method is superior to those of most previously reported label-free methods. Compared with methods that use polymerase chain reaction amplification, this label-free CL method is much simpler, faster, and more economic. This work has thus demonstrated a simple and fast scanning strategy for the detection of specific DNA sequences related to diseases. Graphical Abstract Schematic illustration of label-free CL method for detection of specific DNA sequences.
灵敏、特异、简单、快速且低成本的DNA检测方法在临床诊断、基因治疗及各类生物医学研究中极为重要。在本研究中,我们开发了一种通用方法,用于检测结核分枝杆菌(TB)、乙型肝炎病毒(HBV)和髓细胞瘤病毒癌基因(v-myc)的特定DNA序列。该方法使用同时双功能化有化学发光(CL)试剂和催化金属络合物的金纳米颗粒作为信号报告分子,并以与靶标互补的DNA链作为捕获探针。在这种CL方法中,生物素化的单链DNA捕获探针固定在链霉亲和素包被的微孔板中。加入靶标单链DNA后,捕获探针与靶标DNA杂交。加入双功能化金纳米颗粒和H₂O₂后,获得明确的CL信号,且随着靶标DNA浓度增加,CL强度发生变化。能够测定浓度范围为1.0×10⁻⁹ - 1.0×10⁻⁶ M的靶标TB单链DNA,检测限为4.8×10⁻¹⁰ M。使用这种CL技术,也能够在1.0×10⁻⁹ - 1.0×10⁻⁶ M范围内测定HBV单链DNA和v-myc单链DNA,检测限分别为5.9×10⁻¹⁰ M和8.0×10⁻¹⁰ M。本文报道的方法是第一种利用同时双功能化有CL试剂和催化金属络合物的金纳米颗粒来测定特定DNA序列的无标记CL方法。这种CL方法的灵敏度优于大多数先前报道的无标记方法。与使用聚合酶链反应扩增的方法相比,这种无标记CL方法更简单、快速且经济。因此,本研究展示了一种用于检测与疾病相关的特定DNA序列的简单快速扫描策略。图形摘要:用于检测特定DNA序列的无标记CL方法的示意图。