Division of Biotechnology, University of Turku, Turku, Finland.
Anal Chim Acta. 2013 Apr 15;772:87-92. doi: 10.1016/j.aca.2013.02.029. Epub 2013 Feb 28.
In this report a novel wash-free method for multiplexed DNA detection is demonstrated employing target specific probe pairs and switchable lanthanide luminescence technology on a solid-phase array. Four oligonucleotide capture probes, conjugated at 3' to non-luminescent lanthanide ion carrier chelate, were immobilized as a small array on the bottom of a microtiter plate well onto which a mix of corresponding detection probes, conjugated at 5' to a light absorbing antenna ligand, were added. In the presence of complementary target nucleic acid both the spotted capture probe and the liquid-phase detection probe hybridize adjacently on the target. Consequently the two non-luminescent label molecules self-assemble and form a luminescent mixed lanthanide chelate complex. Lanthanide luminescence is thereafter measured without a wash step from the spots by scanning in time-resolved mode. The homogeneous solid-phase array-based method resulted in quantitative detection of synthetic target oligonucleotides with 0.32 nM and 0.60 nM detection limits in a single target and multiplexed assay, respectively, corresponding to 3× SD of the background. Also qualitative detection of PCR-amplified target from Escherichia coli is described.
在本报告中,展示了一种新颖的免洗方法,用于在固相阵列上使用靶标特异性探针对和可切换的镧系元素发光技术进行多重 DNA 检测。将 4 个寡核苷酸捕获探针固定在微滴定板孔的底部,探针的 3' 端连接非发光镧系离子载体螯合物,用作小阵列,然后将相应的检测探针混合物(5' 端连接吸光天线配体)添加到阵列上。在互补靶核酸存在的情况下,点样捕获探针和液相检测探针在靶标上相邻杂交。结果,两个非发光标记分子自组装并形成发光混合镧系配合物复合物。此后,无需清洗步骤,即可通过时间分辨模式从斑点进行镧系元素发光测量。基于均相固相阵列的方法可实现合成靶标寡核苷酸的定量检测,在单靶标和多重分析中,检测限分别为 0.32 nM 和 0.60 nM,对应于背景的 3×SD。还描述了从大肠杆菌中扩增的靶标的定性检测。