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Improvement of Sensitivity and Dynamic Range in Proximity Ligation Assays by Asymmetric Connector Hybridization

机译:通过非对称连接子杂交改善邻近结扎法的灵敏度和动态范围

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The proximity ligation assay (PLA) is one of the most sensitive and simple protein assays developed to date, yet a major limitation is the relatively narrow dynamic range compared to other assays such as enzyme-linked immunosorbent assays. In this work, the dynamic range of PLA was improved by 2 orders of magnitude and the sensitivity was improved by a factor of 1.57. To accomplish this, asymmetric DNA hybridization was used to reduce the probability of target-independent, background ligation. An experimental model of the aptamer-target-connector complex (apt_(A)-T-apt_(B)-C_(20,PLA)) in PLA was developed to study the effects of asymmetry in aptamer-connector hybridization. Connector base pairing was varied from the PLA standard of 20 total bases (C_(20)) to an asymmetric combination with 15 total bases (C_(15)). The results of this model suggested that weakening the affinity of one side of the connector to one aptamer would significantly reduce target-independent ligation (background) without greatly affecting target-dependent ligation (signal). These predictions were confirmed using PLA with asymmetric connectors for detection of human thrombin. This novel, asymmetric PLA approach should impact any previously developed PLA method (using aptamers or antibodies) by reducing target-independent ligation events, thus generally improving the sensitivity and dynamic range of the assay.
机译:邻近连接测定法(PLA)是迄今为止开发的最敏感,最简单的蛋白质测定法之一,但主要限制是与其他测定法(如酶联免疫吸附测定法)相比,动态范围相对狭窄。在这项工作中,PLA的动态范围提高了2个数量级,灵敏度提高了1.57倍。为此,使用不对称DNA杂交来降低靶标独立背景连接的可能性。建立了PLA适体-靶-连接体复合物(apt_(A)-T-apt_(B)-C_(20,PLA))的实验模型,以研究不对称性在适体-连接体杂交中的作用。连接器的碱基配对从PLA标准的20个总碱基(C_(20))变为具有15个总碱基的非对称组合(C_(15))。该模型的结果表明,削弱连接器一侧对一个适体的亲和力将显着降低靶标无关的连接(背景),而不会大大影响靶标依赖性的连接(信号)。使用带有不对称连接器的PLA检测人凝血酶可以证实这些预测。这种新颖的非对称PLA方法应通过减少靶标无关的连接事件来影响任何先前开发的PLA方法(使用适体或抗体),从而通常提高测定的灵敏度和动态范围。

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