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多臂 RNA 连接,通过输入序列对分子逻辑进行无约束编码,实现多功能无细胞诊断。

Multi-arm RNA junctions encoding molecular logic unconstrained by input sequence for versatile cell-free diagnostics.

机构信息

Biodesign Center for Molecular Design and Biomimetics at the Biodesign Institute, Arizona State University, Tempe, AZ, USA.

BeiGene (Shanghai) Co., Ltd., Shanghai, China.

出版信息

Nat Biomed Eng. 2022 Mar;6(3):298-309. doi: 10.1038/s41551-022-00857-7. Epub 2022 Mar 14.

DOI:10.1038/s41551-022-00857-7
PMID:35288660
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8940621/
Abstract

Applications of RNA-based molecular logic have been hampered by sequence constraints imposed on the input and output of the circuits. Here we show that the sequence constraints can be substantially reduced by appropriately encoded multi-arm junctions of single-stranded RNA structures. To conditionally activate RNA translation, we integrated multi-arm junctions, self-assembled upstream of a regulated gene and designed to unfold sequentially in response to different RNA inputs, with motifs of loop-initiated RNA activators that function independently of the sequence of the input RNAs and that reduce interference with the output gene. We used the integrated RNA system and sequence-independent input RNAs to execute two-input and three-input OR and AND logic in Escherichia coli, and designed paper-based cell-free colourimetric assays that accurately identified two human immunodeficiency virus (HIV) subtypes (by executing OR logic) in amplified synthetic HIV RNA as well as severe acute respiratory syndrome coronavirus-2 (via two-input AND logic) in amplified RNA from saliva samples. The sequence-independent molecular logic enabled by the integration of multi-arm junction RNAs with motifs for loop-initiated RNA activators may be broadly applicable in biotechnology.

摘要

基于 RNA 的分子逻辑的应用受到输入和输出电路的序列限制的阻碍。在这里,我们表明通过适当编码的单链 RNA 结构的多臂连接,可以大大减少序列限制。为了有条件地激活 RNA 翻译,我们整合了多臂连接,该连接在受调控基因的上游自行组装,并设计为响应不同的 RNA 输入顺序展开,与环起始 RNA 激活子的基序相结合,该基序独立于输入 RNA 的序列起作用,并且减少了对输出基因的干扰。我们使用集成的 RNA 系统和与序列无关的输入 RNA 在大肠杆菌中执行了双输入和三输入的 OR 和 AND 逻辑,并设计了基于纸张的无细胞比色测定法,该测定法可以准确识别两种人类免疫缺陷病毒 (HIV) 亚型(通过执行 OR 逻辑)在扩增的合成 HIV RNA 中,以及在唾液样本中扩增的 RNA 中严重急性呼吸综合征冠状病毒 2(通过双输入 AND 逻辑)。通过将多臂连接 RNA 与环起始 RNA 激活子的基序集成,实现的与序列无关的分子逻辑可能在生物技术中具有广泛的应用。

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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ea/8940621/04a8c811d32e/41551_2022_857_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ea/8940621/b36fa19ecf55/41551_2022_857_Fig7_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ea/8940621/a94c792392e9/41551_2022_857_Fig8_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ea/8940621/d8d6ac03ccf3/41551_2022_857_Fig9_ESM.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/40ea/8940621/1acfdf80592e/41551_2022_857_Fig10_ESM.jpg

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