Wu Liang, Manchanda Arushi, Gupta Vipul, Paull Brett
Australian Centre for Research on Separation Science (ACROSS) and ARC Centre of Excellence for Electromaterials Science (ACES), School of Natural Sciences (Chemistry), University of Tasmania, Hobart 7001, Tasmania, Australia.
ACS Omega. 2023 Apr 3;8(15):13569-13577. doi: 10.1021/acsomega.2c06228. eCollection 2023 Apr 18.
A novel, low-cost, and disposable thread-based electrofluidic analytical method employing isotachophoresis (ITP) was developed for demonstrating surface DNA hybridization. This approach was based on graphene oxide (GO) surface-functionalized zones on nylon threads as a binding platform to trap a fluorescently labeled isotachophoretically focused single-stranded DNA (ssDNA) band, resulting in quenching of the fluorescence, which signaled quantitative trapping. In the event of an isotachophoretically focused complementary DNA (cDNA) band passing over the GO-trapped ssDNA zone, surface hybridization of the ssDNA and cDNA to form double-stranded DNA (dsDNA) band occurred, which is released from the GO-coated zones, resulting in restoration of the fluorescent signal as it exits the GO band and migrates further along the thread. This controllable process demonstrates the potential of the GO-functionalized thread-based microfluidic analytical approach for DNA hybridization and its visualization, which could be adapted into point-of-care (POC) diagnostic devices for real-world applications.
开发了一种新颖、低成本且一次性使用的基于丝线的电流体分析方法,该方法采用等速电泳(ITP)来展示表面DNA杂交。这种方法基于尼龙丝上氧化石墨烯(GO)表面功能化区域作为结合平台,以捕获荧光标记的等速电泳聚焦单链DNA(ssDNA)带,导致荧光猝灭,这标志着定量捕获。当等速电泳聚焦的互补DNA(cDNA)带经过GO捕获的ssDNA区域时,ssDNA和cDNA发生表面杂交形成双链DNA(dsDNA)带,该双链DNA带从GO涂层区域释放,导致荧光信号在其离开GO带并沿丝线进一步迁移时恢复。这一可控过程展示了基于GO功能化丝线的微流体分析方法在DNA杂交及其可视化方面的潜力,该方法可应用于即时检测(POC)诊断设备以用于实际应用。