Engineering Research Center of Nano-Geomaterials of Ministry of Education, Faculty of Materials Science and Chemistry , China University of Geosciences , Wuhan 430074 , China.
Institute of Molecular Medicine, Renji Hospital, School of Medicine and School of Chemistry and Chemical Engineering , Shanghai Jiao Tong University , Shanghai 200127 , China.
Anal Chem. 2019 Feb 5;91(3):2021-2027. doi: 10.1021/acs.analchem.8b04434. Epub 2019 Jan 28.
Gold nanoparticles (AuNPs) have shown great promise as a universal platform for biosensing and are often functionalized with a densely packed DNA for intracellular detection. While DNA-AuNP conjugates, such as nanoflares, have been used for single and multiple mRNA molecules detection in living cells, the target recognition reaction is triggered once they enter into cells, making it impossible to control the initial reaction at the desired time. To solve this problem, we have designed photoactivated (PA) nanoflares for intracellular mRNA analysis with high spatiotemporal control. PA nanoflares consist of AuNP and photoresponsive DNA hairpin probes. Without UV irradiation, the DNA hairpin could be kept unawakened and show no reactivity to target the probe. Upon UV activation, the hairpin structures are destroyed and expose the sticky domains, which act as toeholds to mediate strand displacement reactions, making flares release from the gold surface and causing an increase of fluorescence. By tuning light irradiation, PA nanoflares for mRNA detection in living cells can be temporally controlled. With the benefit from two-photon laser illumination, PA nanoflares can detect mRNA in selective cells at a desired time point at the single-cell level. Compared to the traditional nanoflares, the novel PA nanoflares have increased the detection sensitivity and achieved intracellular biomarkers detection at the single-cell level with high spatiotemporal control.
金纳米颗粒(AuNPs)作为生物传感的通用平台具有巨大的应用前景,并且通常通过密集排列的 DNA 进行功能化,以用于细胞内检测。虽然 DNA-AuNP 缀合物,如纳米耀斑,已被用于在活细胞中检测单个和多个 mRNA 分子,但目标识别反应是在它们进入细胞后才被触发的,这使得无法在所需的时间控制初始反应。为了解决这个问题,我们设计了光激活(PA)纳米耀斑,用于具有高时空控制的细胞内 mRNA 分析。PA 纳米耀斑由 AuNP 和光响应 DNA 发夹探针组成。在没有 UV 照射的情况下,DNA 发夹可以保持未激活状态,并且对目标探针没有反应性。在 UV 激活后,发夹结构被破坏并暴露粘性结构域,该结构域充当引发链置换反应的衔接子,使耀斑从金表面释放出来并导致荧光增加。通过调整光照射,可以实现对活细胞中 mRNA 检测的时间控制。利用双光子激光照明的优势,PA 纳米耀斑可以在单细胞水平上在所需的时间点选择性地检测细胞中的 mRNA。与传统的纳米耀斑相比,新型 PA 纳米耀斑提高了检测灵敏度,并实现了单细胞水平的细胞内生物标志物检测,具有高时空控制。