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Microplate based assay for thrombin detection using an RNA aptamer as affinity ligand and cleavage of a chromogenic or a fluorogenic peptide substrate

机译:基于微孔板的凝血酶检测实验,使用RNA适体作为亲和配体并裂解发色或发荧光的肽底物

摘要

The authors report on a microplate based thrombin assay by using an RNA aptamer (Toggle-25) as the affinity ligand. The aptamer is nuclease-resistant because it contains nucleobases modified with 2'-deoxyfluoro saccharides. The aptamer is coated on the surface of the wells of microplates where it captures thrombin from a sample. Following a washing step, a chromogenic or a fluorogenic peptide substrate is added which is cleaved by the captured thrombin to form a yellow product (with absorbance at 405 nm) or a blue fluorescent product (with an emission maximum at 444 nm) after incubation at 37 A degrees C for 2 h. The assay enables thrombin to be determined with a 10 fM detection limit when using the fluorogenic substrate. The assay is selective in that several other proteins do not interfere. The assay can be applied to the determination of thrombin in diluted human serum and plasma.
机译:作者报告了通过使用RNA适体(Toggle-25)作为亲和配体进行的基于微孔板的凝血酶测定。适体是抗核酸酶的,因为它含有被2'-脱氧氟糖修饰的核碱基。适体被包被在微孔板的孔表面上,在那里从样品中捕获凝血酶。洗涤步骤后,加入发色或发荧光的肽底物,将其在捕获的凝血酶下裂解,在室温下温育后形成黄色产物(在405 nm处有吸光度)或蓝色荧光产物(在444 nm处有最大发射)。 37摄氏度2小时。当使用荧光底物时,该测定法能够以10 fM的检测限确定凝血酶。该测定是选择性的,因为其他几种蛋白质也不会干扰。该测定法可用于测定稀释的人血清和血浆中的凝血酶。

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  • 作者

    Hao Lihua; Zhao Qiang;

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  • 年度 2016
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