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A generative model for constructing nucleic acid sequences binding to a protein

机译:一种用于构建与蛋白质结合的核酸序列的生成模型

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BACKGROUND:Interactions between protein and nucleic acid molecules are essential to a variety of cellular processes. A large amount of interaction data generated by high-throughput technologies have triggered the development of several computational methods either to predict binding sites in a sequence or to determine whether a pair of sequences interacts or not. Most of these methods treat the problem of the interaction of nucleic acids with proteins as a classification problem rather than a generation problem.RESULTS:We developed a generative model for constructing single-stranded nucleic acids binding to a target protein using a long short-term memory (LSTM) neural network. Experimental results of the generative model are promising in the sense that DNA and RNA sequences generated by the model for several target proteins show high specificity and that motifs present in the generated sequences are similar to known protein-binding motifs.CONCLUSIONS:Although these are preliminary results of our ongoing research, our approach can be used to generate nucleic acid sequences binding to a target protein. In particular, it will help design efficient in vitro experiments by constructing an initial pool of potential aptamers that bind to a target protein with high affinity and specificity.
机译:背景:蛋白质和核酸分子之间的相互作用对各种细胞过程至关重要。由高吞吐量技术产生的大量交互数据已经触发了几种计算方法的开发,可以在序列中预测绑定站点或确定一对序列是否相互作用。这些方法中的大多数将核酸与蛋白质相互作用的问题作为分类问题而不是一代问题。结果:我们开发了一种用于使用长短短期构建与靶蛋白结合的单链核酸的生成模型内存(LSTM)神经网络。发电机模型的实验结果是有意义的,即由几个靶蛋白的模型产生的DNA和RNA序列显示出高特异性,并且产生的序列中存在的基序类似于已知的蛋白质结合基序。结论:虽然这些是初步的我们正在进行的研究结果,我们的方法可用于产生与靶蛋白结合的核酸序列。特别是,它将通过构建与具有高亲和力和特异性的靶蛋白结合的潜在适体的初始池来帮助设计高效的体外实验。

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