State Key Laboratory of Chemo/Biosensing and Chemometrics, College of Biology, College of Chemistry and Chemical Engineering, Hunan University, Changsha 410082, PR China.
Biosens Bioelectron. 2011 Oct 15;28(1):450-3. doi: 10.1016/j.bios.2011.05.038. Epub 2011 Jun 1.
Cocaine is one of the most abused drugs in the United States and is potentially dangerous when consumed in excess. Its detection is thus important in many areas in the fight against drug trafficking. We have developed an amplified detection method for cocaine based on a strand-displacement polymerization reaction using aptamer recognition. The system mainly consists of a hairpin probe with Cy5 labeled on its 3' end, a primer with FAM labeled on its 5' end, and polymerase. The aptamer sequence is integrated into the 5'-section of the hairpin probe. The primer is designed complementary to the 3' end of the hairpin probe, which is also part of the hairpin stem region. The cocaine induced reaction cycle generates product for detection and thus for signal amplification. The detection limit of this method is 200 nM in about 16 min and the specificity of this approach is excellent. We believe that this strategy will be useful for the development of analytical schemes for a variety of aptamers for small molecules, metal ions, and proteins. This simple scheme employing the strand-displacement polymerization reaction may find wide application in forensic analysis, environmental monitoring, and clinical diagnostics.
可卡因是美国最滥用的毒品之一,过量摄入时具有潜在危险。因此,在打击毒品贩运的许多领域,可卡因的检测都很重要。我们开发了一种基于适体识别的链置换聚合反应的可卡因放大检测方法。该系统主要由带有 Cy5 标记的发夹探针、带有 FAM 标记的引物和聚合酶组成。适体序列整合到发夹探针的 5' 端。引物设计与发夹探针的 3' 端互补,该 3' 端也是发夹茎区的一部分。可卡因诱导的反应循环产生用于检测和信号放大的产物。该方法的检测限约为 16 分钟内 200 nM,该方法的特异性非常好。我们相信,这种策略将有助于开发用于小分子、金属离子和蛋白质的各种适体的分析方案。这种简单的方案采用链置换聚合反应,可能会在法医分析、环境监测和临床诊断中得到广泛应用。