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 in | Angewandte Chemie International Edition Vol. 58; no. 19; pp. 6333 - 6337 |
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Main Authors | , , , , |
Format | Journal Article |
Language | English |
Published |
Germany
Wiley Subscription Services, Inc
06.05.2019
John Wiley and Sons Inc |
Edition | International ed. in English |
Subjects | |
Online Access | Get full text |
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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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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1433-7851 1521-3773 1521-3773 |
DOI: | 10.1002/anie.201901469 |