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Self-selection of dissipative assemblies driven by primitive chemical reaction networks
Open accessAbstract
Life is a dissipative nonequilibrium structure that requires constant consumption of energy to sustain itself. How such an unstable state could have selected from an abiotic pool of molecules remains a mystery. Here we show that liquid phase-separation offers a mechanism for the selection of dissipative products from a library of reacting molecules. We bring a set of primitive carboxylic acids out-of-equilibrium by addition of high-energy condensing agents. The resulting anhydrides are transiently present before deactivation via hydrolysis. We find the anhydrides that phase-separate into droplets to protect themselves from hydrolysis and to be more persistent than non-assembling ones. Thus, after several starvation-refueling cycles, the library self-selects the phase-separating anhydrides. We observe that the self-selection mechanism is more effective when the library is brought out-of-equilibrium by periodic addition of batches as opposed to feeding it continuously. Our results suggest that phase-separation offers a selection mechanism for energy dissipating assemblies.
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Cited by
Stimuli responsive dynamic transformations in supramolecular gels
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A short peptide synthon for liquid–liquid phase separation
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Metadata
- Authors
- Tena-Solsona, M., Wanzke, C., Riess, B., Bausch, A. R., & Boekhoven, J.
- Venue
- Nature Communications
- Published
- 2018-05-23
- Volume
- 9
- Issue
- 1
- Pages
- 2044-2044
- ISSN
- 2041-1723 (ISSN-L)
- OpenAlex
- W2803795590
- Cited by
- 196
- References
- 6
- FWCI
- 13.80
- Type
- journal article
- Language
- en
- Open access
- gold
- Licence
- creativecommons.org/licenses/by/4.0 (tdm)
- creativecommons.org/licenses/by/4.0 (vor)
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