China National Narcotics Control Commission, China Pharmaceutical University, Joint Laboratory on Key Technologies of Narcotics Control, No. 24 Tongjiaxiang Road, Nanjing 210009, China.
Key Laboratory of Drug Monitoring and Control, Drug Intelligence and Forensic Center, Ministry of Public Security, No. 18 Dongbeiwang West Road, Beijing 100193, China.
Anal Chem. 2022 Jun 21;94(24):8715-8723. doi: 10.1021/acs.analchem.2c01103. Epub 2022 Jun 7.
The target of typical PCR analysis is restricted to nucleic acids. To this end, we report here a novel strategy to simultaneously detect genetic and metabolic markers using commercial PCR kits with cucurbit[8]urils (CB[8]) implemented to manipulate the activity of Taq DNA polymerase. CB[8] binds with the nonionic surfactants and displaces them from the polymerase surface, resulting in decreased enzyme activity. Meanwhile, the inhibited enzyme can be reversibly activated when spermine, the downstream metabolite of ornithine decarboxylase (ODC), is present in the sample, which competitively binds to CB[8] and recovers polymerase activity. CB[8] was implemented in conventional PCR kits not only to reduce false-positive results but also to extend the detection range of PCR technology. With this novel method to detect ODC in cell lysates containing both the nucleotides and intracellular metabolites, positive results were only observed in highly active HEK 293T cells, whereas silent cells treated with ODC inhibitor showed negative readouts, therefore providing a simple but elegant dual-modality PCR method for precision diagnosis.
典型的 PCR 分析的目标仅限于核酸。为此,我们在这里报告了一种使用葫芦[8]脲(CB[8])的商业 PCR 试剂盒同时检测遗传和代谢标志物的新策略,该策略用于操纵 Taq DNA 聚合酶的活性。CB[8]与非离子表面活性剂结合,并将它们从聚合酶表面置换出来,导致酶活性降低。同时,当样品中存在精脒(鸟氨酸脱羧酶(ODC)的下游代谢物)时,被抑制的酶可以被可逆地激活,它与 CB[8]竞争结合并恢复聚合酶活性。CB[8]被应用于常规 PCR 试剂盒中,不仅可以减少假阳性结果,还可以扩展 PCR 技术的检测范围。使用这种检测细胞裂解物中 ODC 的新方法,该方法包含核苷酸和细胞内代谢物,只有在高度活跃的 HEK 293T 细胞中才观察到阳性结果,而用 ODC 抑制剂处理的沉默细胞显示阴性结果,因此为精准诊断提供了一种简单而优雅的双模态 PCR 方法。