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Using fluoro modified RNA aptamers as affinity ligands on magnetic beads for sensitive thrombin detection through affinity capture and thrombin catalysis

机译:使用氟修饰的RNA适体作为磁珠上的亲和配体,通过亲和捕获和凝血酶催化进行敏感的凝血酶检测

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Many RNA aptamers against a variety of targets have been selected, and some of the RNA aptamers can have better binding affinity than DNA aptamers. The application of RNA aptamers against thrombin in bio-analysis previously did not attract enough attention due to the high cost in synthesis and poor stability of RNA aptamers, compared with the wide use of DNA aptamers. Here we present a sensitive and specific assay for thrombin by using a nuclease-resistant fluoro (F) modified RNA aptamer (Toggle-25) as an affinity ligand on magnetic beads to explore the capability of this RNA aptamer for thrombin detection and expand its application. This RNA aptamer had high binding affinity and good stability. The RNA aptamers were immobilized on the magnetic beads to selectively capture thrombin, and then thrombin cleaved fluorogenic or chromogenic peptide substrates. The measurement of the generated product allowed the final detection of thrombin. This assay reached a detection limit of 10 fM when a fluorogenic substrate was used. Thrombin could be successfully detected in diluted human serum. This work shows that the applied RNA aptamer Toggle-25 is a good alternative to DNA aptamers of thrombin as an affinity ligand, and it can be used in developing assays for thrombin. Other assays for thrombin can be expected by using this RNA aptamer with a different detection format.
机译:已经选择了许多针对多种靶标的RNA适体,并且一些RNA适体可以具有比DNA适体更好的结合亲和力。与DNA适体相比,RNA适体的合成成本高,且RNA适体的稳定性差,以前在生物分析中针对凝血酶的RNA适体的应用并未引起足够的重视。在这里,我们通过使用抗核酸酶的氟(F)修饰的RNA适体(Toggle-25)作为磁珠上的亲和配体,对凝血酶进行灵敏和特异的检测,以探索该RNA适体用于凝血酶检测的能力并扩展其应用。该RNA适体具有高结合亲和力和良好的稳定性。将RNA适体固定在磁珠上以选择性地捕获凝血酶,然后将凝血酶切割成荧光或发色的肽底物。测量所产生的产物可以最终检测凝血酶。当使用荧光底物时,该测定法的检测极限达到了10 fM。可以在稀释的人血清中成功检测到凝血酶。这项工作表明,所应用的RNA适体Toggle-25是凝血酶DNA适体作为亲和配体的良好替代品,可用于开发凝血酶检测方法。通过使用具有不同检测格式的这种RNA适体,可以预期其他凝血​​酶测定方法。

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