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PhD position

PhD in Using microfluidics to observe and manipulate coacervate droplets

University of Groningen · Groningen, Netherlands

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At a glance

Project focus
We are looking for a 4-year PhD candidate to join our nationally funded, multi-partner research consortium, Towards De-Novo Life.

PhD position at University of Groningen: key facts

Opportunity type
PhD position
Organization
University of Groningen
Location
Groningen, Netherlands
Field / discipline
Not specified
Application deadline
12 Oct 2026
Funding / compensation
Paid
Duration
See source description
Last source check
No source check recorded

About this phd position at University of Groningen

Original title: PhD position Using microfluidics to observe and manipulate coacervate droplets

We are looking for a 4-year PhD candidate to join our nationally funded, multi-partner research consortium, Towards De-Novo Life. The main aim of this interdisciplinary project is to achieve minimal life based on chemical rather than biological components such as DNA, proteins or other macromolecules. Our PhD candidate will contribute by developing new microfluidic tools to work with micrometer-sized coacervate droplets, the compartments in which chemical replication, growth and evolution will take place.

What are you going to do?

The de-novo synthesis of life requires integrating the essential features of life, which include replication (the ability to copy oneself), metabolism (promoting the formation of one’s own components from material in the environment) and compartmentalization (keeping the internal components together and separate from the environment) into a system that is maintained out of equilibrium. Key to the creation of a minimal form of life is Darwinian evolution of the resulting synthetic cell-like systems. Serving as the compartments in our work are coacervate microdroplets, consisting of a very dense aqueous phase containing a high concentration of macromolecules. Because coacervates can exist in dilute aqueous phases without loss of droplet structure, they can act as cell-like spheres without the need of a membrane to contain their content.

In this project, you will use microfluidics to create a first-generation platform to achieve growth and division of micrometer-sized coacervate droplets. You will then consider populations of coacervate droplets confined in a second, more complex microfluidic platform, monitoring their growth and mutation rates. “Mother” droplets will be followed alongside their “daughters” using fluorescence microscopy, with addition of precursor materials (“nutrients”) and random removal of individuals (“death”).

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