Join us
We are always looking for talented postdoctoral researchers and PhD candidates who are interested in origins of life, synthetic cells, coacervates, physical biology and multi-omics analysis methods in general, who like to work in an interdisciplinary cutting-edge environment. If you are interested in joining, please contact us directly to explore fellowship opportunities (please include a CV, and two academic references).
Internships
The Huck group is the ideal environment for students looking for interdisciplinary science. The group is a diverse, multinational team, and you will not only get in depth training in the topic of your internship, but will also develop a broad view on cutting edge science. Interested: contact the supervisors listed in the project descriptions for more information, or contact Wilhelm directly.
Open positions
Specific positions will be advertised here when available.
Research projects/Internships
| Title | Keywords | Project description | Supervisor | Image |
|---|---|---|---|---|
| Development of high- throughput platforms for cancer diagnosis | Microfluidics, Cell culture, Flow cytometry, Sequencing, -omics, Patients’ material | The goal of this project is to develop a high-throughput fluidic platform for single-cell detection of cells contributing to the metastatic process. You will work on a platform that will provide a breakthrough technology for future downstream single-cell multi-omics analysis and for monitoring of treatment efficacy in cancer patients. | Kinga Matuła, Francesca Rivello |  |
| Construction of a noise-cancelling enzymatic reaction network | Microfluidics, synthesis (SPPS, Schlenk techniques), Flow chemistry, Kinetics | The goal of this project is to realize the construction of a noise-cancelling enzymatic reaction network under out-of-equilibrium conditions. Throughout the project, you will work at the interface of organic synthesis, flow-chemistry, enzymology and photocatalysis. | Michael Teders |  |
| Studying dynamics of cell response using single-cell omic tools | Microfluidics, Cell culture, data analysis, -omics, Biochemistry, Molecular biology, Flow cytometry, Immunoassays, Sequencing, Patients’ material | The aim of this project is to further our understanding of how biochemical information flows through cells upon external, dynamic stimulation (e.g. drugs) and during disease progression. You will work on the development and application of a platform for single-cell (phospho)proteome and transcriptome analysis to study cell response. | Kinga Matuła, Jessie van Buggenum, Francesca Rivello, Erik van Buijtenen, Melde Witmond |  |
| Building a synthetic cell: reconstituting E. coli’s proteome in a cell-free system | Cell-free expression, 2D gel Electrophoresis, Click chemistry, Bacterial cell culture, Lysate Fabrication, Genome isolation | To build a synthetic cell it is important to know if cell-free protein expression can be performed on a genome wide scale. Therefore, the aim of the project is to visualize and compare, using non-natural amino acid incorporation and 2D gel electrophoresis, the proteome expressed from E. coli genomes both in cells (in vivo) as well as cell-free (in vitro). | Andrei Sakai, Roel Maas |  |
| Analysis of single-cell sequencing results and implementation of new tools | Bioinformatics, Single-cell omics | The aim of this project is to develop, combine and use state-of-the art bioinformatics tools for single-cell multi-omics analysis. In particular, we are interested in understanding how biochemical information flows through cells upon external stimulation (e.g. drugs) and during disease progression. To study cell response, sequencing results will be generated using a platform for single-cell (phospho)proteome and transcriptome analysis. | Francesca Rivello, Jessie van Buggenum, Melde Witmond |  |
| Constructing a glucose dependent neuron | Molecular computing, Carbohydrate synthesis, Enzymes, Neuron | In this project you will be working on building an artificial neuron, the smallest unit of a neural network, making use of enzymes and photoprotected glucose. It will be your job to synthesize a photoprotected glucose, to measure the rate constants and to make a model of the neuron itself. | Jeroen van de Wiel |   |
| Studying bacterial protein coacervation in vitro, in droplets, and in liposomes | Biochemistry, Enzyme purification, NusA, DPS, FtsZ, Microfluidics, IVTT | In this project, we aim to explore several (confirmed) candidate proteins involved in bacterial liquid-liquid phase separation (LLPS) in an in vitro setting. Proteins will be purified, and their phase behaviour will be investigated in vitro, in droplets, and in liposomes. This project is part of a larger collaborative effort to investigate bacterial LLPS. | Ludo Schoenmakers |  |
| Synthetic cell construction in Giant Unilamellar Vesicles (GUVs) | Synthetic biology, GUV formation, Microfluidics, Membrane protein insertion, IVTT | In this project, we aim at constructing synthetic cell-like structures in Giant Unilamellar Vesicles (GUVs) using a number of different approaches. The key aim is to realize robust communication between the inside and outside environment of synthetic cells by way of the membrane protein inserting membrane protein: the Sec translocon. | Ludo Schoenmakers |  |
| Exploring chemotypic diversity in prebiotic reaction networks. | Prebiotic chemistry, Reaction networks, Kinetics, Data analysis, Air sensitive handling, HPLC, GC-MS, Machine learning methods | The self-organisation of reaction pathways from abiotic precursors was a vital component in the transition from inanimate to animate matter. In this project, we wish to understand the principles for how abiotic environments shaped the development of modern biochemical pathways. You will explore the incorporation of redox reactions and alpha-ketoacids into the formose reaction. | Will Robinson, Peer van Duppen, Elena Daines |  |
| Uniting Metabolism and Information Replication at the Origins of Life | Prebiotic Chemistry, (Oligo)Ribonucleotides, Chemical Reaction Networks, PAGE gels, Mass Spectrometry | In the biochemistry of extant Life there is an intimate link between metabolism and information replication+transfer found in ribonucleotides and their reactions. In this project we aim to trace this link all the way back to the origins of Life by constructing oligonucleotide-based chemical reaction networks that can demonstrate both metabolic and information replication functions. | Oliver Maguire |  |
| Environmental dynamics as a driving force for the organization of chemical reaction networks | Origin of life, Chemical reaction networks, Flow chemistry, Python modelling, HPLC, GC-MS, Python, Machine learning | The network of metabolic reactions in Life is postulated to find its origin in prebiotic waters, in the absence of sophisticated enzymes or genetic inheritance. We hypothesize environmental dynamics were a fundamental driving force for the organization of chemical reaction networks. In this project, you will simulate a changing environment by imposing temporal patterns on the network via modulation of the inflow profile of catalyst or feedstock molecules. | Peer van Duppen |  |