Modulation of Higher‐order Behaviour in Model Protocell Communities by Artificial Phagocytosis

Collective behaviour in mixed populations of synthetic protocells is an unexplored area of bottom‐up synthetic biology. The dynamics of a model protocell community is exploited to modulate the function and higher‐order behaviour of mixed populations of bioinorganic protocells in response to a proces...

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Published inAngewandte Chemie International Edition Vol. 58; no. 19; pp. 6333 - 6337
Main Authors Rodríguez‐Arco, Laura, Kumar, B. V. V. S. Pavan, Li, Mei, Patil, Avinash J., Mann, Stephen
Format Journal Article
LanguageEnglish
Published Germany Wiley Subscription Services, Inc 06.05.2019
John Wiley and Sons Inc
EditionInternational ed. in English
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Summary:Collective behaviour in mixed populations of synthetic protocells is an unexplored area of bottom‐up synthetic biology. The dynamics of a model protocell community is exploited to modulate the function and higher‐order behaviour of mixed populations of bioinorganic protocells in response to a process of artificial phagocytosis. Enzyme‐loaded silica colloidosomes are spontaneously engulfed by magnetic Pickering emulsion (MPE) droplets containing complementary enzyme substrates to initiate a range of processes within the host/guest protocells. Specifically, catalase, lipase, or alkaline phosphatase‐filled colloidosomes are used to trigger phagocytosis‐induced buoyancy, membrane reconstruction, or hydrogelation, respectively, within the MPE droplets. The results highlight the potential for exploiting surface‐contact interactions between different membrane‐bounded droplets to transfer and co‐locate discrete chemical packages (artificial organelles) in communities of synthetic protocells. The modulation of higher‐order behaviour in model protocell communities was investigated. Enzyme‐loaded silica colloidosomes are spontaneously engulfed by magnetic Pickering emulsion (MPE) droplets containing complementary enzyme substrates to initiate a range of processes within the host–guest protocells.
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ISSN:1433-7851
1521-3773
1521-3773
DOI:10.1002/anie.201901469