Institute of Microanalytical Systems, Department of Chemistry, Zhejiang University, Hangzhou, 310058, China.
Talanta. 2011 Sep 30;85(4):1760-5. doi: 10.1016/j.talanta.2011.06.075. Epub 2011 Jul 7.
In this paper, a nanoliter droplet array based on enzymatic stem-loop probes ligation and SYBR Green real-time PCR for quantification of microRNA was developed. By employing T4 RNA ligase 2 instead of T4 DNA ligase, we designed simplified stem-loop probes to perform microRNA-templated DNA ligation and reduced the non-specific ligation of T4 DNA ligase. SYBR green I dye was employed instead of TaqMan probes in present miniaturized real-time PCR systems. Specifically, we optimized the dosage of SYBR Green I dye in nanoliter droplet and verified the performance of this system by detecting synthetic mir-122 with a 6 logs dynamic range (from 1.5 × 10(5) to 1.5 × 10(10) copies). Linear relationship of the standard curve (R(2)=0.9997) and high PCR amplification efficiency (96.83%) were obtained under the optimized conditions. We detected the expression of mir-122 across five mouse tissues and the result was consistent with that TaqMan microRNA assay. We think this miniaturized real-time PCR platform reduced the detection cost considerably, thus showing the great potential to quantitative biology.
本文基于酶切环探针连接和 SYBR Green 实时 PCR 建立了纳升级液滴阵列,用于定量检测 microRNA。通过使用 T4 RNA 连接酶 2 代替 T4 DNA 连接酶,我们设计了简化的茎环探针来进行 microRNA 模板化 DNA 连接,并减少了 T4 DNA 连接酶的非特异性连接。在当前的微型化实时 PCR 系统中,我们使用 SYBR Green I 染料代替 TaqMan 探针。具体来说,我们优化了纳升级液滴中 SYBR Green I 染料的剂量,并通过检测合成 mir-122 来验证该系统的性能,检测范围为 6 个对数动态范围(从 1.5×10(5)到 1.5×10(10)拷贝)。在优化条件下,获得了标准曲线的线性关系(R(2)=0.9997)和高 PCR 扩增效率(96.83%)。我们在五个小鼠组织中检测了 mir-122 的表达,结果与 TaqMan microRNA 检测一致。我们认为这种微型化实时 PCR 平台大大降低了检测成本,因此在定量生物学方面具有很大的潜力。