College of Biology, Hunan University, Changsha, 410082, China.
Department of Rehabilitation, The Second Xiangya Hospital, Central South University, Changsha, 410011, China.
Talanta. 2019 Dec 1;205:120092. doi: 10.1016/j.talanta.2019.06.092. Epub 2019 Jul 3.
VEGF mRNA, as an important biomarker for disease diagnosis and therapeutics, has received extensive attention. However, how to monitor its mRNA levels rapidly and sensitively remains a challenge. Herein, a strategy was designed for facile and efficient detection of VEGF mRNA and imaging in living cells using a collaborative system of a fluorophore-labeled single-stranded probe (P), reduced graphene oxide (rGO) and double-specific nuclease (DSN). The combination of strong fluorophore-quenching ability of rGO with DSN assisted signal amplification contributes to the superior sensitivity of the assay for VEGF mRNA, which was reflected by the lower limit of mRNA detection of 100 fM obtained using dual signal amplification manner. Furthermore, the developed sensor was directly used for intracellular mRNA imaging in vitro without the assistance of transfection reagent. In summary, the simple, ultra-sensitive and cost-effective mRNA assay system, which provided a general analysis strategy for other mRNAs assay by replacing the sequence of the probe, is hopeful for applying on the clinical diagnosis and therapy.
VEGF mRNA 作为疾病诊断和治疗的重要生物标志物,受到了广泛关注。然而,如何快速、灵敏地监测其 mRNA 水平仍然是一个挑战。本文设计了一种使用荧光标记的单链探针(P)、还原氧化石墨烯(rGO)和双特异性核酸酶(DSN)协同系统,在活细胞中简便、高效地检测 VEGF mRNA 并进行成像的策略。rGO 与 DSN 辅助信号放大的强荧光猝灭能力的结合,使该方法对 VEGF mRNA 的检测具有超高的灵敏度,通过双信号放大方式,检测到的 mRNA 的下限低至 100 fM。此外,该传感器无需转染试剂的辅助,可直接用于体外细胞内 mRNA 成像。总之,这种简单、超灵敏、经济高效的 mRNA 分析系统,通过替换探针序列,为其他 mRNA 分析提供了一种通用的分析策略,有望应用于临床诊断和治疗。