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Affinity capillary electrophoresis with laser induced fluorescence detection for thrombin analysis using nuclease-resistant RNA aptamers

机译:亲和毛细管电泳,激光诱导荧光检测,使用抗核酸酶的RNA适体对凝血酶进行分析

摘要

Aptamer affinity capillary electrophoresis coupled with laser-induced fluorescence (CE-LIF) combines the advantages of affinity aptamer, rapid CE separation, and high sensitivity detection. Here we reported an affinity CE-LIF assay for thrombin by using a fluorophore-labeled RNA aptamer containing 2'-fluoro modification in sugar rings of pyrimidine nucleotides (C and U) as affinity ligand. This RNA aptamer has high binding affinity, specificity and biostability. Thrombin at 0.2 nM was successfully detected. This RNA aptamer allowed for the detection of thrombin spiked in diluted human serum sample due to the nuclease resistance. The RNA aptamer has comparable binding affinity to a 29-mer DNA aptamer for thrombin, and the binding site of the RNA aptamer on thrombin partially overlaps with the binding site of the 29-mer DNA aptamer on thrombin. It shows the nuclease-resistant RNA aptamers are promising in assays for thrombin. (C) 2016 Elsevier B.V. All rights reserved.
机译:适体亲和毛细管电泳与激光诱导荧光(CE-LIF)结合,具有亲和适体,快速CE分离和高灵敏度检测的优点。在这里,我们报告了通过使用荧光团标记的RNA适体对凝血酶的亲和CE-LIF分析,该适体在嘧啶核苷酸(C和U)的糖环中包含2'-氟修饰作为亲和配体。该RNA适体具有高结合亲和力,特异性和生物稳定性。成功检测到0.2 nM的凝血酶。由于核酸酶的抗性,这种RNA适体允许检测稀释的人血清样品中掺入的凝血酶。 RNA适体与凝血酶的29-mer DNA适体具有可比的结合亲和力,并且凝血酶上的RNA适体的结合位点与凝血酶上29-mer DNA适体的结合位点部分重叠。它表明耐核酸酶的RNA适体在凝血酶的测定中很有希望。 (C)2016 Elsevier B.V.保留所有权利。

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