利用 M13 Phagemid 和基于 CRISPR 的基因调控技术进行细胞间通信,在大肠杆菌中实现多细胞计算

Hadiastri Kusumawardhani, Florian Zoppi, Roberto Avendaño, Yolanda Schaerli
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引用次数: 0

摘要

在多细胞联合体中,信息处理分布在不同的特化细胞类型中,这为实现复杂的生物计算系统提供了一种前景广阔的策略。然而,在合成细菌联合体内建立正交的细胞间通信(或称 "导线")仍是一大挑战。在本研究中,我们将噬菌体介导的细胞间通信与基于 CRISPR 的基因调控相结合,在合成大肠杆菌联合体内实现多细胞计算,从而解决了这一瓶颈问题。我们通过调控 M13 噬菌体上编码的单导 RNA(sgRNA)从发送者细胞向接收者细胞的转移来实现细胞间通信。一旦进入接收细胞,转移的 sgRNA 通过 CRISPR 干扰介导基因调控。利用这种方法,我们成功构建了单输入、双输入和四输入逻辑门。我们的工作拓展了细胞间通信的工具包,为合成微生物联合体中的复杂信息处理铺平了道路,具有生物计算、生物传感和生物制造等多种潜在应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Engineering Intercellular Communication using M13 Phagemid and CRISPR-based Gene Regulation for Multicellular Computing in Escherichia coli
Engineering multicellular consortia, where information processing is distributed across specialized cell types, offers a promising strategy for implementing sophisticated biocomputing systems. However, a major challenge remains in establishing orthogonal intercellular communication, or "wires," within synthetic bacterial consortia. In this study, we address this bottleneck by integrating phagemid-mediated intercellular communication with CRISPR-based gene regulation for multicellular computing in synthetic E. coli consortia. We achieve intercellular communication by regulating the transfer of single guide RNAs (sgRNAs) encoded on M13 phagemids from sender to receiver cells. Once inside the receiver cells, the transferred sgRNAs mediate gene regulation via CRISPR interference. Leveraging this approach, we successfully constructed one-, two-, and four-input logic gates. Our work expands the toolkit for intercellular communication and paves the way for complex information processing in synthetic microbial consortia, with diverse potential applications, including biocomputing, biosensing, and biomanufacturing.
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