Self-selection of dissipative assemblies driven by primitive chemical reaction networks

Marta Tena-Solsona, Caren Wanzke, Benedikt Riess, Andreas R. Bausch, Job Boekhoven

Research output: Contribution to journalArticlepeer-review

136 Scopus citations

Abstract

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.

Original languageEnglish
Article number2044
JournalNature Communications
Volume9
Issue number1
DOIs
StatePublished - 1 Dec 2018

Fingerprint

Dive into the research topics of 'Self-selection of dissipative assemblies driven by primitive chemical reaction networks'. Together they form a unique fingerprint.

Cite this