Department of Chemistry, University of Illinois at Urbana-Champaign, Urbana, Illinois 61801, USA.
Nat Chem. 2011 Jul 24;3(9):697-703. doi: 10.1038/nchem.1092.
Portable, low-cost and quantitative detection of a broad range of targets at home and in the field has the potential to revolutionize medical diagnostics and environmental monitoring. Despite many years of research, very few such devices are commercially available. Taking advantage of the wide availability and low cost of the pocket-sized personal glucose meter-used worldwide by diabetes sufferers-we demonstrate a method to use such meters to quantify non-glucose targets, ranging from a recreational drug (cocaine, 3.4 µM detection limit) to an important biological cofactor (adenosine, 18 µM detection limit), to a disease marker (interferon-gamma of tuberculosis, 2.6 nM detection limit) and a toxic metal ion (uranium, 9.1 nM detection limit). The method is based on the target-induced release of invertase from a functional-DNA-invertase conjugate. The released invertase converts sucrose into glucose, which is detectable using the meter. The approach should be easily applicable to the detection of many other targets through the use of suitable functional-DNA partners (aptamers, DNAzymes or aptazymes).
便携式、低成本且能够在现场和家庭中对广泛目标进行定量检测,这有可能彻底改变医学诊断和环境监测。尽管已经进行了多年的研究,但市面上此类设备却寥寥无几。我们利用随处可见且价格低廉的袖珍型个人血糖仪(被糖尿病患者广泛使用),展示了一种利用此类血糖仪定量检测非葡萄糖目标物的方法,包括从消遣性药物(可卡因,检测限 3.4µM)到重要生物辅因子(腺苷,检测限 18µM),再到疾病标志物(结核干扰素-γ,检测限 2.6nM)和有毒金属离子(铀,检测限 9.1nM)。该方法基于目标诱导的功能性 DNA-蔗糖酶偶联物从酶中释放出蔗糖酶。释放出的蔗糖酶将蔗糖转化为葡萄糖,然后可以使用血糖仪进行检测。通过使用合适的功能性 DNA 配体(适体、DNA 酶或适体酶),该方法应该很容易适用于检测许多其他目标物。