Department of Chemistry, East China Normal University, Shanghai 200062, China.
Talanta. 2010 Mar 15;80(5):1868-72. doi: 10.1016/j.talanta.2009.10.036. Epub 2009 Oct 28.
An aptamer-based assay for thrombin with high specificity and sensitivity was presented. In the protocol, the aptamer for thrombin was immobilized on magnetic nanoparticle, and its complementary oligonucleotide was labeled with gold nanoparticles, then the aptamer was hybridized with the complementary oligonucleotide to form the duplex structure as a probe, this probe could be used for the specific recognition for thrombin. In the presence of thrombin, the aptamer prefer to form the G-quarter structure with thrombin, resulting in the dissociation of the duplex of the probe and the release of the gold labeled oligonucleotide. Upon this, we were able to detect thrombin through the detection of the electrochemical signal of gold nanoparticles. The strategy combines with the high specificity of aptamer and the excellent characteristics of nanoparticles. This assay is simple, rapid, sensitive and highly specific, it does not require labeling of thrombin, and it could be applied to detect thrombin in complex real sample. The method shows great potential in other protein analysis and in disease diagnosis.
本文提出了一种基于适体的高特异性和高灵敏度凝血酶检测方法。在该方案中,凝血酶适体固定在磁性纳米颗粒上,其互补寡核苷酸标记有金纳米颗粒,然后适体与互补寡核苷酸杂交形成双链结构作为探针,该探针可用于对凝血酶的特异性识别。在凝血酶存在的情况下,适体优先与凝血酶形成 G-四链体结构,导致探针双链解离并释放标记的金寡核苷酸。通过检测金纳米颗粒的电化学信号,我们可以检测到凝血酶。该策略结合了适体的高特异性和纳米颗粒的优异特性。该检测方法简单、快速、灵敏、特异性高,不需要对凝血酶进行标记,可用于检测复杂实际样本中的凝血酶。该方法在其他蛋白质分析和疾病诊断中具有很大的应用潜力。
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