IDEAS home Printed from https://ideas.repec.org/a/nat/natcom/v13y2022i1d10.1038_s41467-022-31898-w.html
   My bibliography  Save this article

Building programmable multicompartment artificial cells incorporating remotely activated protein channels using microfluidics and acoustic levitation

Author

Listed:
  • Jin Li

    (Cardiff University, The Parade)

  • William D. Jamieson

    (Cardiff University)

  • Pantelitsa Dimitriou

    (Cardiff University, The Parade)

  • Wen Xu

    (Cardiff University)

  • Paul Rohde

    (Victor Chang Cardiac Research Institute)

  • Boris Martinac

    (Victor Chang Cardiac Research Institute
    School of Clinical Medicine, UNSW)

  • Matthew Baker

    (School of Biotechnology and Biomolecular Science, UNSW)

  • Bruce W. Drinkwater

    (University of Bristol)

  • Oliver K. Castell

    (Cardiff University)

  • David A. Barrow

    (Cardiff University, The Parade)

Abstract

Intracellular compartments are functional units that support the metabolism within living cells, through spatiotemporal regulation of chemical reactions and biological processes. Consequently, as a step forward in the bottom-up creation of artificial cells, building analogous intracellular architectures is essential for the expansion of cell-mimicking functionality. Herein, we report the development of a droplet laboratory platform to engineer complex emulsion-based, multicompartment artificial cells, using microfluidics and acoustic levitation. Such levitated models provide free-standing, dynamic, definable droplet networks for the compartmentalisation of chemical species. Equally, they can be remotely operated with pneumatic, heating, and magnetic elements for post-processing, including the incorporation of membrane proteins; alpha-hemolysin; and mechanosensitive channel of large-conductance. The assembly of droplet networks is three-dimensionally patterned with fluidic input configurations determining droplet contents and connectivity, whilst acoustic manipulation can be harnessed to reconfigure the droplet network in situ. The mechanosensitive channel can be repeatedly activated and deactivated in the levitated artificial cell by the application of acoustic and magnetic fields to modulate membrane tension on demand. This offers possibilities beyond one-time chemically mediated activation to provide repeated, non-contact, control of membrane protein function. Collectively, this expands our growing capability to program and operate increasingly sophisticated artificial cells as life-like materials.

Suggested Citation

  • Jin Li & William D. Jamieson & Pantelitsa Dimitriou & Wen Xu & Paul Rohde & Boris Martinac & Matthew Baker & Bruce W. Drinkwater & Oliver K. Castell & David A. Barrow, 2022. "Building programmable multicompartment artificial cells incorporating remotely activated protein channels using microfluidics and acoustic levitation," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
  • Handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31898-w
    DOI: 10.1038/s41467-022-31898-w
    as

    Download full text from publisher

    File URL: https://www.nature.com/articles/s41467-022-31898-w
    File Function: Abstract
    Download Restriction: no

    File URL: https://libkey.io/10.1038/s41467-022-31898-w?utm_source=ideas
    LibKey link: if access is restricted and if your library uses this service, LibKey will redirect you to where you can use your library subscription to access this item
    ---><---

    References listed on IDEAS

    as
    1. Eduardo Perozo & D. Marien Cortes & Pornthep Sompornpisut & Anna Kloda & Boris Martinac, 2002. "Open channel structure of MscL and the gating mechanism of mechanosensitive channels," Nature, Nature, vol. 418(6901), pages 942-948, August.
    2. Qingchuan Li & Shubin Li & Xiangxiang Zhang & Weili Xu & Xiaojun Han, 2020. "Programmed magnetic manipulation of vesicles into spatially coded prototissue architectures arrays," Nature Communications, Nature, vol. 11(1), pages 1-9, December.
    3. Thomas Beneyton & Dorothee Krafft & Claudia Bednarz & Christin Kleineberg & Christian Woelfer & Ivan Ivanov & Tanja Vidaković-Koch & Kai Sundmacher & Jean-Christophe Baret, 2018. "Out-of-equilibrium microcompartments for the bottom-up integration of metabolic functions," Nature Communications, Nature, vol. 9(1), pages 1-10, December.
    4. Roberta Kwok, 2010. "Five hard truths for synthetic biology," Nature, Nature, vol. 463(7279), pages 288-290, January.
    5. Yang Song & Thomas C. T. Michaels & Qingming Ma & Zhou Liu & Hao Yuan & Shuichi Takayama & Tuomas P. J. Knowles & Ho Cheung Shum, 2018. "Budding-like division of all-aqueous emulsion droplets modulated by networks of protein nanofibrils," Nature Communications, Nature, vol. 9(1), pages 1-7, December.
    6. Philip Ball, 2004. "Starting from scratch," Nature, Nature, vol. 431(7009), pages 624-626, October.
    7. Alessandro Alcinesio & Oliver J. Meacock & Rebecca G. Allan & Carina Monico & Vanessa Restrepo Schild & Idil Cazimoglu & Matthew T. Cornall & Ravinash Krishna Kumar & Hagan Bayley, 2020. "Controlled packing and single-droplet resolution of 3D-printed functional synthetic tissues," Nature Communications, Nature, vol. 11(1), pages 1-13, December.
    8. Henrike Niederholtmeyer & Cynthia Chaggan & Neal K. Devaraj, 2018. "Communication and quorum sensing in non-living mimics of eukaryotic cells," Nature Communications, Nature, vol. 9(1), pages 1-8, December.
    9. Zan Hua & Joseph R. Jones & Marjolaine Thomas & Maria C. Arno & Anton Souslov & Thomas R. Wilks & Rachel K. O’Reilly, 2019. "Anisotropic polymer nanoparticles with controlled dimensions from the morphological transformation of isotropic seeds," Nature Communications, Nature, vol. 10(1), pages 1-8, December.
    Full references (including those not matched with items on IDEAS)

    Most related items

    These are the items that most often cite the same works as this one and are cited by the same works as this one.
    1. Songyang Liu & Yanwen Zhang & Xiaoxiao He & Mei Li & Jin Huang & Xiaohai Yang & Kemin Wang & Stephen Mann & Jianbo Liu, 2022. "Signal processing and generation of bioactive nitric oxide in a model prototissue," Nature Communications, Nature, vol. 13(1), pages 1-12, December.
    2. Xiangxiang Zhang & Chao Li & Fukai Liu & Wei Mu & Yongshuo Ren & Boyu Yang & Xiaojun Han, 2022. "High-throughput production of functional prototissues capable of producing NO for vasodilation," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    3. Nasimul Noman & Taku Monjo & Pablo Moscato & Hitoshi Iba, 2015. "Evolving Robust Gene Regulatory Networks," PLOS ONE, Public Library of Science, vol. 10(1), pages 1-21, January.
    4. Javier Macia & Romilde Manzoni & Núria Conde & Arturo Urrios & Eulàlia de Nadal & Ricard Solé & Francesc Posas, 2016. "Implementation of Complex Biological Logic Circuits Using Spatially Distributed Multicellular Consortia," PLOS Computational Biology, Public Library of Science, vol. 12(2), pages 1-24, February.
    5. Yongcheng Jin & Ellina Mikhailova & Ming Lei & Sally A. Cowley & Tianyi Sun & Xingyun Yang & Yujia Zhang & Kaili Liu & Daniel Catarino da Silva & Luana Campos Soares & Sara Bandiera & Francis G. Szele, 2023. "Integration of 3D-printed cerebral cortical tissue into an ex vivo lesioned brain slice," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
    6. Richard Booth & Ignacio Insua & Sahnawaz Ahmed & Alicia Rioboo & Javier Montenegro, 2021. "Supramolecular fibrillation of peptide amphiphiles induces environmental responses in aqueous droplets," Nature Communications, Nature, vol. 12(1), pages 1-8, December.
    7. Nishkantha Arulkumaran & Mervyn Singer & Stefan Howorka & Jonathan R. Burns, 2023. "Creating complex protocells and prototissues using simple DNA building blocks," Nature Communications, Nature, vol. 14(1), pages 1-13, December.
    8. Shubin Li & Yingming Zhao & Shuqi Wu & Xiangxiang Zhang & Boyu Yang & Liangfei Tian & Xiaojun Han, 2023. "Regulation of species metabolism in synthetic community systems by environmental pH oscillations," Nature Communications, Nature, vol. 14(1), pages 1-10, December.
    9. Bob Sluijs & Roel J. M. Maas & Ardjan J. Linden & Tom F. A. Greef & Wilhelm T. S. Huck, 2022. "A microfluidic optimal experimental design platform for forward design of cell-free genetic networks," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    10. Hui Sun & Shuai Chen & Xiao Li & Ying Leng & Xiaoyan Zhou & Jianzhong Du, 2022. "Lateral growth of cylinders," Nature Communications, Nature, vol. 13(1), pages 1-9, December.
    11. Jonathan Mount & Grigory Maksaev & Brock T. Summers & James A. J. Fitzpatrick & Peng Yuan, 2022. "Structural basis for mechanotransduction in a potassium-dependent mechanosensitive ion channel," Nature Communications, Nature, vol. 13(1), pages 1-11, December.
    12. Tristan Ursell & Kerwyn Casey Huang & Eric Peterson & Rob Phillips, 2007. "Cooperative Gating and Spatial Organization of Membrane Proteins through Elastic Interactions," PLOS Computational Biology, Public Library of Science, vol. 3(5), pages 1-10, May.
    13. Kenjiro Yoshimura & Kazuko Iida & Hidetoshi Iida, 2021. "MCAs in Arabidopsis are Ca2+-permeable mechanosensitive channels inherently sensitive to membrane tension," Nature Communications, Nature, vol. 12(1), pages 1-9, December.
    14. Jorik Waeterschoot & Willemien Gosselé & Špela Lemež & Xavier Casadevall i Solvas, 2024. "Artificial cells for in vivo biomedical applications through red blood cell biomimicry," Nature Communications, Nature, vol. 15(1), pages 1-17, December.
    15. Nylund, Petra A. & Ferràs-Hernández, Xavier & Pareras, Luis & Brem, Alexander, 2022. "The emergence of entrepreneurial ecosystems based on enabling technologies: Evidence from synthetic biology," Journal of Business Research, Elsevier, vol. 149(C), pages 728-735.
    16. Lorenzo Pasotti & Nicolò Politi & Susanna Zucca & Maria Gabriella Cusella De Angelis & Paolo Magni, 2012. "Bottom-Up Engineering of Biological Systems through Standard Bricks: A Modularity Study on Basic Parts and Devices," PLOS ONE, Public Library of Science, vol. 7(7), pages 1-10, July.

    More about this item

    Statistics

    Access and download statistics

    Corrections

    All material on this site has been provided by the respective publishers and authors. You can help correct errors and omissions. When requesting a correction, please mention this item's handle: RePEc:nat:natcom:v:13:y:2022:i:1:d:10.1038_s41467-022-31898-w. See general information about how to correct material in RePEc.

    If you have authored this item and are not yet registered with RePEc, we encourage you to do it here. This allows to link your profile to this item. It also allows you to accept potential citations to this item that we are uncertain about.

    If CitEc recognized a bibliographic reference but did not link an item in RePEc to it, you can help with this form .

    If you know of missing items citing this one, you can help us creating those links by adding the relevant references in the same way as above, for each refering item. If you are a registered author of this item, you may also want to check the "citations" tab in your RePEc Author Service profile, as there may be some citations waiting for confirmation.

    For technical questions regarding this item, or to correct its authors, title, abstract, bibliographic or download information, contact: Sonal Shukla or Springer Nature Abstracting and Indexing (email available below). General contact details of provider: http://www.nature.com .

    Please note that corrections may take a couple of weeks to filter through the various RePEc services.

    IDEAS is a RePEc service. RePEc uses bibliographic data supplied by the respective publishers.