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Autonomous helical propagation of active toroids with mechanical action

Author

Listed:
  • Bowen Shen

    (Jilin University)

  • Youliang Zhu

    (Chinese Academy of Sciences)

  • Yongju Kim

    (Jilin University)

  • Xiaobin Zhou

    (Jilin University)

  • Haonan Sun

    (Jilin University)

  • Zhongyuan Lu

    (Jilin University)

  • Myongsoo Lee

    (Jilin University)

Abstract

Self-assembly in nature is fundamentally dynamic, existing in out-of-equilibrium state in which the systems have the ability to autonomously respond to environmental changes. However, artificial systems exist in a global minimum state, which are incapable of conducting such complex functions. Here we report that input of thermal energy can trigger fixed, artificial toroids to spontaneously nucleate helical growth. The helical polymerization undergoes reversible and repeatable cycles with subsequent energy input. When the toroids are located inside lipid vesicles, the polymerization-depolymerization cycle is accompanied by reversible elongation of spherical vesicles. Such liberation from a global minimum state will pave the way to create emergent structures with functions as complex as those of living systems.

Suggested Citation

  • Bowen Shen & Youliang Zhu & Yongju Kim & Xiaobin Zhou & Haonan Sun & Zhongyuan Lu & Myongsoo Lee, 2019. "Autonomous helical propagation of active toroids with mechanical action," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
  • Handle: RePEc:nat:natcom:v:10:y:2019:i:1:d:10.1038_s41467-019-09099-9
    DOI: 10.1038/s41467-019-09099-9
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    Cited by:

    1. Michael D. Dore & Muhammad Ghufran Rafique & Tianxiao Peter Yang & Marlo Zorman & Casey M. Platnich & Pengfei Xu & Tuan Trinh & Felix J. Rizzuto & Gonzalo Cosa & Jianing Li & Alba Guarné & Hanadi F. S, 2024. "Heat-activated growth of metastable and length-defined DNA fibers expands traditional polymer assembly," Nature Communications, Nature, vol. 15(1), pages 1-13, December.

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