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A novel method of screening thrombin-inhibiting DNA aptamers using an evolution-mimicking algorithm

机译:一种采用进化模拟算法筛选抑制凝血酶的DNA适体的新方法

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摘要

Thrombin-inhibiting DNA aptamers have already been obtained through the systematic evolution of ligands by exponential enrichment (SELEX). However, SELEX is a method that screens DNA aptamers that bind to their target molecules, and it sometimes fails to screen good inhibitors. Therefore, it is necessary to develop a method of screening DNA aptamers based on their inhibitory effects on the target molecules. We developed a novel method of detecting aptamers using an evolution-mimicking algorithm, and we applied it to the search of new aptamers which inhibit thrombin. First, we randomly designed and synthesized ten 15mer oligonucleotides presumed to form G-quartet structures, and then measured their thrombin-inhibiting activities. The aptamers showing high inhibitory activity were selected, and we shuffled and mutated those sequences in silico to generate 10 new sequences of next-generation aptamers. After repeating the cycle five times, we successfully obtained the same aptamers reported previously, and they showed high inhibitory activity. In addition, we added 8mer oligonucleotides to both the 5′ and the 3′ end of the selected 15mer aptamers, and then repeated the evolution in silico. After two cycles, we were able to obtain aptamers with higher inhibitory activity than that of the 15mer aptamers.
机译:抑制凝血酶的DNA适体已经通过配体通过指数富集(SELEX)的系统进化而获得。但是,SELEX是一种筛选与目标分子结合的DNA适体的方法,有时无法筛选出良好的抑制剂。因此,有必要开发一种基于DNA适体对靶分子的抑制作用的筛选方法。我们开发了一种使用进化模拟算法检测适体的新方法,并将其应用于抑制凝血酶的新适体的搜索。首先,我们随机设计和合成了十个15mer寡核苷酸,这些寡核苷酸被认为可以形成G四重结构,然后测量它们的凝血酶抑制活性。选择显示出高抑制活性的适体,然后我们对这些序列进行计算机改组和突变,以生成10个新的下一代适体序列。重复五次循环后,我们成功获得了先前报道的相同适体,并显示出高抑制活性。此外,我们在所选的15mer适体的5'和3'末端都添加了8mer寡核苷酸,然后通过计算机重复进化。经过两个周期,我们能够获得比15mer适体具有更高抑制活性的适体。

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