利用结构预测深度生成设计 RNA 配合物。

IF 12 Q1 COMPUTER SCIENCE, INTERDISCIPLINARY APPLICATIONS
Felix Wong, Dongchen He, Aarti Krishnan, Liang Hong, Alexander Z Wang, Jiuming Wang, Zhihang Hu, Satotaka Omori, Alicia Li, Jiahua Rao, Qinze Yu, Wengong Jin, Tianqing Zhang, Katherine Ilia, Jack X Chen, Shuangjia Zheng, Irwin King, Yu Li, James J Collins
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引用次数: 0

摘要

RNA 是一类可编程的生物大分子,能够发挥多种生物功能。最近的研究开发出了精确的 RNA 三维结构预测方法,从而可以在结构引导下设计新的 RNA。在这里,我们开发了一个结构到序列的深度学习平台,用于从头生成设计 RNA 合体。我们的研究表明,我们的方法可以设计出与已知的发光适配体结构相似但序列不同的 RNA 适配体,这些适配体在小分子存在时会发出荧光。我们通过实验验证了几种生成的 RNA 合体具有荧光活性,表明这些合体可以在硅学中进行活性优化,并发现它们的荧光机制与已知的发光合体类似。我们的研究结果表明,结构预测可以指导有针对性地设计新的 RNA 序列,并节约资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Deep generative design of RNA aptamers using structural predictions.

RNAs represent a class of programmable biomolecules capable of performing diverse biological functions. Recent studies have developed accurate RNA three-dimensional structure prediction methods, which may enable new RNAs to be designed in a structure-guided manner. Here, we develop a structure-to-sequence deep learning platform for the de novo generative design of RNA aptamers. We show that our approach can design RNA aptamers that are predicted to be structurally similar, yet sequence dissimilar, to known light-up aptamers that fluoresce in the presence of small molecules. We experimentally validate several generated RNA aptamers to have fluorescent activity, show that these aptamers can be optimized for activity in silico, and find that they exhibit a mechanism of fluorescence similar to that of known light-up aptamers. Our results demonstrate how structural predictions can guide the targeted and resource-efficient design of new RNA sequences.

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CiteScore
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