Department of Chemistry, Imperial College London, Exhibition Road, London, SW7 2AZ, UK.
Nat Commun. 2017 Nov 16;8(1):1552. doi: 10.1038/s41467-017-01584-3.
The capability to screen a range of proteins at the single-molecule level with enhanced selectivity in biological fluids has been in part a driving force in developing future diagnostic and therapeutic strategies. The combination of nanopore sensing and nucleic acid aptamer recognition comes close to this ideal due to the ease of multiplexing, without the need for expensive labelling methods or extensive sample pre-treatment. Here, we demonstrate a fully flexible, scalable and low-cost detection platform to sense multiple protein targets simultaneously by grafting specific sequences along the backbone of a double-stranded DNA carrier. Protein bound to the aptamer produces unique ionic current signatures which facilitates accurate target recognition. This powerful approach allows us to differentiate individual protein sizes via characteristic changes in the sub-peak current. Furthermore, we show that by using DNA carriers it is possible to perform single-molecule screening in human serum at ultra-low protein concentrations.
在生物流体中以增强的选择性对一系列蛋白质进行单分子水平筛选的能力,在一定程度上推动了未来诊断和治疗策略的发展。由于易于实现多重检测,而无需昂贵的标记方法或广泛的样品预处理,因此纳米孔传感和核酸适体识别的结合接近这一理想状态。在这里,我们展示了一种完全灵活、可扩展且低成本的检测平台,通过在双链 DNA 载体的主链上嫁接特定序列,可以同时感测多个蛋白质靶标。与适体结合的蛋白质会产生独特的离子电流特征,从而便于准确识别靶标。这种强大的方法使我们能够通过亚峰电流的特征变化来区分单个蛋白质的大小。此外,我们还表明,通过使用 DNA 载体,可以在超低蛋白质浓度下在人血清中进行单分子筛选。