Wu Dan, Xin Xia, Pang Xuehui, Pietraszkiewicz Marek, Hozyst Robert, Sun Xian'ge, Wei Qin
‡National Engineering Technology Research Center for Colloidal Materials, Shandong University, Jinan 250100, China.
§Institute of Physical Chemistry, Polish Academy of Sciences, Kasprzaka 44/52, 01-224 Warsaw, Poland.
ACS Appl Mater Interfaces. 2015 Jun 17;7(23):12663-70. doi: 10.1021/acsami.5b03381. Epub 2015 Jun 2.
A novel electrochemiluminescent (ECL) aptasensor was proposed for the determination of thrombin (TB) using exonuclease-catalyzed target recycling and hybridization chain reaction (HCR) to amplify the signal. The capture probe was immobilized on an Au-GS-modified electrode through a Au-S bond. Subsequently, the hybrid between the capture probe and the complementary thrombin binding aptamer (TBA) was aimed at obtaining double-stranded DNA (dsDNA). The interaction between TB and its aptamer led to the dissociation of dsDNA because TB has a higher affinity to TBA than the complementary strands. In the presence of exonuclease, aptamer was selectively digested and TB could be released for target recycling. Extended dsDNA was formed through HCR of the capture probe and two hairpin DNA strands (NH2-DNA1 and NH2-DNA1). Then, numerous europium multiwalled carbon nanotubes (Eu-MWCNTs) could be introduced through amidation reaction between NH2-terminated DNA strands and carboxyl groups on the Eu-MWCNTs, resulting in an increased ECL signal. The multiple amplification strategies, including the amplification of analyte recycling and HCR, and high ECL efficiency of Eu-MWCNTs lead to a wide linear range (1.0×10(-12)-5.0×10(-9) mol/L) and a low detection limit (0.23 pmol/L). The method was applied to serum sample analysis with satisfactory results.
提出了一种新型电化学发光(ECL)适配体传感器,用于凝血酶(TB)的测定,该传感器利用核酸外切酶催化的目标物循环和杂交链式反应(HCR)来放大信号。捕获探针通过Au-S键固定在金-谷胱甘肽修饰电极上。随后,捕获探针与互补凝血酶结合适配体(TBA)之间的杂交旨在获得双链DNA(dsDNA)。TB与其适配体之间的相互作用导致dsDNA解离,因为TB对TBA的亲和力高于互补链。在核酸外切酶存在下,适配体被选择性消化,TB被释放用于目标物循环。通过捕获探针与两条发夹DNA链(NH2-DNA1和NH2-DNA1)的HCR形成延伸的dsDNA。然后,通过NH2末端DNA链与Eu-MWCNTs上羧基之间的酰胺化反应可引入大量铕多壁碳纳米管(Eu-MWCNTs),从而增加ECL信号。多种放大策略,包括分析物循环放大和HCR,以及Eu-MWCNTs的高ECL效率导致宽线性范围(1.0×10(-12)-5.0×10(-9) mol/L)和低检测限(0.23 pmol/L)。该方法应用于血清样本分析,结果令人满意。