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De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation

Author

Listed:
  • Pei Du

    (Chinese Academy of Sciences)

  • Huiwei Zhao

    (Chinese Academy of Sciences
    University of Chinese Academy of Science)

  • Haoqian Zhang

    (Bluepha Co., Ltd
    Peking University)

  • Ruisha Wang

    (Chinese Academy of Sciences
    University of Chinese Academy of Science)

  • Jianyi Huang

    (Chinese Academy of Sciences
    University of Chinese Academy of Science)

  • Ye Tian

    (Chinese Academy of Sciences)

  • Xudong Luo

    (Chinese Academy of Sciences)

  • Xunxun Luo

    (Chinese Academy of Sciences
    University of Chinese Academy of Science)

  • Min Wang

    (Chinese Academy of Sciences)

  • Yanhui Xiang

    (Chinese Academy of Sciences)

  • Long Qian

    (Peking University)

  • Yihua Chen

    (Chinese Academy of Sciences
    University of Chinese Academy of Science)

  • Yong Tao

    (Chinese Academy of Sciences
    University of Chinese Academy of Science)

  • Chunbo Lou

    (University of Chinese Academy of Science
    Chinese Academy of Sciences)

Abstract

Intercellular signaling is indispensable for single cells to form complex biological structures, such as biofilms, tissues and organs. The genetic tools available for engineering intercellular signaling, however, are quite limited. Here we exploit the chemical diversity of biological small molecules to de novo design a genetic toolbox for high-performance, multi-channel cell–cell communications and biological computations. By biosynthetic pathway design for signal molecules, rational engineering of sensing promoters and directed evolution of sensing transcription factors, we obtain six cell–cell signaling channels in bacteria with orthogonality far exceeding the conventional quorum sensing systems and successfully transfer some of them into yeast and human cells. For demonstration, they are applied in cell consortia to generate bacterial colony-patterns using up to four signaling channels simultaneously and to implement distributed bio-computation containing seven different strains as basic units. This intercellular signaling toolbox paves the way for engineering complex multicellularity including artificial ecosystems and smart tissues.

Suggested Citation

  • Pei Du & Huiwei Zhao & Haoqian Zhang & Ruisha Wang & Jianyi Huang & Ye Tian & Xudong Luo & Xunxun Luo & Min Wang & Yanhui Xiang & Long Qian & Yihua Chen & Yong Tao & Chunbo Lou, 2020. "De novo design of an intercellular signaling toolbox for multi-channel cell–cell communication and biological computation," Nature Communications, Nature, vol. 11(1), pages 1-11, December.
  • Handle: RePEc:nat:natcom:v:11:y:2020:i:1:d:10.1038_s41467-020-17993-w
    DOI: 10.1038/s41467-020-17993-w
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    Cited by:

    1. Xianglai Li & Zhao Zhou & Wenna Li & Yajun Yan & Xiaolin Shen & Jia Wang & Xinxiao Sun & Qipeng Yuan, 2022. "Design of stable and self-regulated microbial consortia for chemical synthesis," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    2. Lin Wang & Xi Zhang & Chenwang Tang & Pengcheng Li & Runtao Zhu & Jing Sun & Yunfeng Zhang & Hua Cui & Jiajia Ma & Xinyu Song & Weiwen Zhang & Xiang Gao & Xiaozhou Luo & Lingchong You & Ye Chen & Zhuo, 2022. "Engineering consortia by polymeric microbial swarmbots," Nature Communications, Nature, vol. 13(1), pages 1-13, December.
    3. Alice Boo & Tyler Toth & Qiguo Yu & Alexander Pfotenhauer & Brandon D. Fields & Scott C. Lenaghan & C. Neal Stewart & Christopher A. Voigt, 2024. "Synthetic microbe-to-plant communication channels," Nature Communications, Nature, vol. 15(1), pages 1-16, December.
    4. Brian D. Huang & Dowan Kim & Yongjoon Yu & Corey J. Wilson, 2024. "Engineering intelligent chassis cells via recombinase-based MEMORY circuits," Nature Communications, Nature, vol. 15(1), pages 1-17, December.

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