IMEC, Kapeldreef 75, Leuven, Belgium.
Biosens Bioelectron. 2011 Mar 15;26(7):3121-6. doi: 10.1016/j.bios.2010.12.008. Epub 2010 Dec 14.
In this report, we demonstrate a label-free genosensor based on DNA hairpins coupled to gold coated sensor surfaces. The hairpin probes were labeled with a thiolated moiety for immobilization at the 5' end and with a fluorophore for signal transduction at the 3' end. In the absence of the complement, the fluorophore is quenched by energy transfer to the gold surface. Addition of the target sequence leads to the hairpin unfolding, and releases the fluorescent signal. This built-in property, using a gold film as both the immobilizing substrate and quenching agent, has the advantage of simplicity in design and ease of further integration. Our results showed that lengths of both the stem and the loop structures have significant effects on the sensor performance. Hybridization kinetics was investigated for various probe/target lengths and concentrations. An optimized hairpin probe gave a fluorescent signal increase of 39 folds after hybridization, which is much higher than the earlier reported results. A limit of detection (LOD) down to 0.3 nM for the complementary target DNA detection has been achieved. The developed sensor was further successfully applied for the detection of single-base mismatch targets, as well as for the direct detection of PCR products.
在本报告中,我们展示了一种基于 DNA 发夹与金涂覆传感器表面偶联的无标记基因传感器。发夹探针在 5' 端用硫醇部分标记以用于固定,在 3' 端用荧光团标记以用于信号转导。在不存在互补序列的情况下,荧光团通过与金表面的能量转移而被猝灭。靶序列的加入导致发夹展开,并释放荧光信号。这种内置特性,使用金膜作为固定化基底和猝灭剂,具有设计简单和易于进一步集成的优点。我们的结果表明,茎和环结构的长度都对传感器性能有显著影响。研究了各种探针/靶序列长度和浓度下的杂交动力学。经过优化的发夹探针在杂交后荧光信号增加了 39 倍,这远高于早期报道的结果。对于互补靶 DNA 的检测,检测限(LOD)低至 0.3 nM。该传感器还成功地应用于单碱基错配靶的检测,以及用于直接检测 PCR 产物。