Projects per year
Abstract
Two different artificial predation strategies are spatially and temporally coupled to generate a simple tit-for-tat mechanism in a ternary protocell network capable of antagonistic enzyme-mediated interactions. The consortium initially consists of protease-sensitive glucose-oxidase-containing proteinosomes (1), non-interacting pH-sensitive polypeptide/mononucleotide coacervate droplets containing proteinase K (2), and proteinosome-adhered pH-resistant polymer/polysaccharide coacervate droplets (3). On receiving a glucose signal, secretion of protons from 1 triggers the disassembly of 2 and the released protease is transferred to 3 to initiate a delayed contact-dependent killing of the proteinosomes and cessation of glucose oxidase activity. Our results provide a step towards complex mesoscale dynamics based on programmable response-retaliation behavior in artificial protocell consortia.
Original language | English |
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Pages (from-to) | 17758-17763 |
Number of pages | 6 |
Journal | Angewandte Chemie - International Edition |
Volume | 58 |
Issue number | 49 |
Early online date | 22 Oct 2019 |
DOIs | |
Publication status | Published - 25 Nov 2020 |
Research Groups and Themes
- BrisSynBio
- Bristol BioDesign Institute
Keywords
- coacervate
- enzyme
- proteinosome
- response-retaliation behavior
- synthetic protocell
- Synthetic biology
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Dive into the research topics of 'Response-Retaliation Behavior in Synthetic Protocell Communities'. Together they form a unique fingerprint.Projects
- 1 Finished
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BrisSynBio: Bristol Centre for Synthetic Biology
Woolfson, D. N. (Principal Investigator)
31/07/14 → 31/03/22
Project: Research