School of Chemical Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea.
School of Advanced Materials Science and Engineering, Sungkyunkwan University, Suwon, Gyeonggi-do, South Korea.
Sci Rep. 2017 Oct 18;7(1):13499. doi: 10.1038/s41598-017-13456-3.
Since the delivery kinetics of different cell types are different, the signal from the target cell is greatly affected by the noise signal of the diagnostic system. This is a major obstacle hindering the practical application of intracellular diagnostic systems, such as tumor heterogeneity. To address these issues, here we present a microRNA detection platform using fluorescence-encoded nanostructured DNA-based probes. The nanostructured DNA was designed to include molecular beacons for detecting cytosolic microRNA as well as additional fluorophores. When the intracellular diagnostic system is delivered, fluorescence signals are generated by the molecular beacons, depending on the concentration of the target microRNA. The fluorescence signals are then normalized to the intensity of the additional fluorophore. Through this simple calculation, the concentration of intracellular microRNA can be determined without interference from the diagnosis system itself. And also it enabled discrimination of microRNA expression heterogeneity in five different breast cancer cell lines.
由于不同细胞类型的释放动力学不同,因此目标细胞的信号会受到诊断系统噪声信号的很大影响。这是阻碍细胞内诊断系统(如肿瘤异质性)实际应用的主要障碍。为了解决这些问题,我们在这里提出了一种使用荧光编码纳米结构 DNA 探针进行 microRNA 检测的平台。纳米结构 DNA 被设计为包含分子信标,用于检测细胞质 microRNA 以及其他荧光团。当递送到细胞内诊断系统时,分子信标根据目标 microRNA 的浓度产生荧光信号。然后将荧光信号归一化为附加荧光团的强度。通过这种简单的计算,可以确定细胞内 microRNA 的浓度,而不会受到诊断系统本身的干扰。并且还能够区分五种不同乳腺癌细胞系中 microRNA 表达的异质性。