Although continuing technical advances in analytical chemistry allow us to measure complex data with relative ease, analyzing such data is a field of science on its own. Fully exploiting the valuable information you were (or were not) looking for from measured data is exactly the expertise we have at the department for chemometrics. We focus on the development of new or improved data analysis methods, but also on the application of established methods on new types of measurements. Chemometrics finds many practical applications, including but not limited to food safety, healthcare, industrial processing and sustainability. If you would like to contribute to such work, check our website and/or contact us for more information on current projects and internship subjects!

The principal focus of Aquatic Ecology and Environmental Biology is to unravel biogeochemical and ecological key processes explaining the functioning and services of wetland ecosystems - covering freshwater, brackish and marine systems - including the interactions between organisms, surface waters, sediments, groundwaters and the atmosphere. Particular attention is payed to environmental pressures such as enhanced nitrogen deposition, eutrophication and  global warming and their effects on the carbon, nitrogen, phosphorus and sulfur cycling. We apply our biogeochemical and ecological insights in the conservation and restoration of wetland ecosystems including lakes and rivers (conservation biology) and in sustainable solutions for water treatment and agriculture. For our research, the analysis of relevant processes in the field situation is combined with experiments in the field, and in the greenhouse, in mesocosms and microcosms both outdoors and in the lab. Several internship possibilities are announced on the website. Tailor made internships related to ongoing projects are often possible. Please contact Bjorn Robroek to discuss whether your interests match with our possibilities.

The transition towards a circular society requires us to design new materials and chemistries. This grand challenges requires radically new ways of doing chemical research.
To address this challenge, the Big Chemistry Robotlab uses robots and artificial intelligence to accelerate the discovery of complex molecular systems and formulations for biomedicine and materials science.
We focus strongly on finding new ways to study, quantify and understand how molecules interact with each other. Depending on the project, there is a more academic focus, or close collaboration with industrial partners.

Currently, the Robotlab is focusing on 3 key questions:

• How can we predict the solubility and volatility of organic molecules to ultimately make better food and cosmetics?
• How can we design green alternatives to environmentally harmful surfactants, such as PFAS, with identical performance?
• How can we design biobased and biodegradable materials for biotechnological and medical applications?

These questions can only be answered by a diverse team of researchers at the interface of chemistry, engineering, biotechnology and AI. We therefore welcome BSc. and MSc. students from all of these backgrounds, either individually or as teams. For more info, reach out to william.robinson@ru.nl and/or mathijs.mabesoone@ru.nl.

Peptides display many different characteristics, both structural and functional, based on their amino acid sequence and secondary conformation. In the bio-organic chemistry group we synthesize peptides and try to manipulate their structure and function. These peptides form the building blocks to create new materials for tissue engineering and synthetic vaccines. Moreover, peptides are employed in our group for the design of molecules to diagnose and treat cancer by specifically delivering drugs to diseased cells.

What is your blood group? A, B, or O? Did you know that this is determined by complex sugar molecules called glycans? Glycans cover the suface of every cell in the body. They are composed of different carbohydrates that assemble into a dazzling amount of structurally diverse sugar chains. Next to constituting the blood groups, glycans regulate immune recognition and instruct the intestinal microbiome. Moreover, glycan alterations are involved in every major disease.

Our lab uses gene editing (CRISPR) to control the glycan structures that cells produce to build so called cell-based glycan arrays, with each cell presenting only a specific glycan structure. This enables the production of defined glycans that are applied to modulate the immune system and the gut microbiome. Furthermore, the cell-based glycan array allows us to engineer “diseased” glycans and to recapitulate their role in pathological processes such as inflammation and autoimmunity. Ultimately, our aim is to develop novel glycan-based therapies that reduce inflammation and foster a healthy gut microbiome.

Why do two identical cells look different? Cell-to-cell variability (i.e. noise) in gene expression leads to large differences in mRNA and protein levels in cells. This variability can hamper the treatment of diseases such as HIV and cancer. Due to the architectural complexity of a cell a multitude of factors can be identified that heavily influence reaction dynamics, causing gene expression to deviate from predictable behavior. We combine single-molecule and time lapse imaging with cell-free biochemistry approaches to discern key physical, kinetic, and gene circuit-based factors that determine the outcome of cellular reactions at a single-cell level.

Carbohydrates are the most abundant biomolecules on earth. They play an essential role in biology as a source of energy and regulate many biological processes. We develop new chemistry to synthesize carbohydrate molecules with a variety of applications. The main topics and projects in the group are listed below. Depending on the project we are able to host chemistry, biology or molecular life science internships. Some of the projects are in collaboration with partners from industry. 

Stereoselective glycosylation reactions: We develop new chemical methodology to prepare complex carbohydrates via stereoselective glycosylation reactions. To this end, we also study the reaction mechanism of these reactions.  

Carbohydrates as drugs: We design and synthesize carbohydrate based drugs toward the treatment of cancer, pathogenic infections and immune deficiencies. Furthermore, we perform cellular tests to evaluate the biological activity of the molecules that we prepare. 

Carbohydrate food ingredients and allergies: We synthesize carbohydrate food ingredients and study their health benefits and allergy profiles.   

Carbohydrate based personal care products: We design, synthesize and test carbohydrate molecules for the personal care application (cosmetics etc). 

If you are interested in one or more of these projects, feel free to contact us for more information

DNA packaging into the nucleus of a cell is a topological organization problem that needs to be precisely regulated, as the genome needs to control the accessibility of the information it encodes. DNA organization occurs on several levels, all involving physical processes. The basic folding of the genome is dictated by principles of polymer physics, active systems driven by molecular motors result in DNA loops, and division into nuclear compartments is regulated by the equilibrium thermodynamics of phase separation. Our lab aims to examine the functional relevance of nuclear architecture and the biophysical mechanisms that drive it. We use a multifaceted and interdisciplinary approach, ranging from cellular- and single-molecule biophysics to engineering.

Our group focuses on comprehensively determining epigenetic/chromatin/nuclear architectural changes and which of those may be driving cellular ageing. We have successfully generated high-quality single-cell datasets in-house which are currently being analysed using a variety of bioinformatic approaches.

Our group is dedicated to investigating the mechanisms underlying human skin stem cells renewal & differentiation. We focus on studying the epigenetic machinery, which involves chemical modifications of DNA and the role of non-coding RNA molecules. By exploring how different genes and cellular processes work together, we aim to uncover the secrets behind the robustness and precision of biological systems.

In many neurodevelopmental disorders, including Intellectual Disability (ID) or Schizophrenia, (risk) gene mutations have been identified that directly or indirectly alter neuronal maturation, signaling and neuronal network organization.

In our group for "Cellular Neurophysiology" at the CNS dept, Radboudumc, we are focussing on mutations of epigenetic modifiers that have been found to be causative for ID or Schizophrenia in patients. We aim to reveal the molecular and cellular mechanisms leading to neuronal network dysfunction and to identify new potential targets for therapy.

To this end we make use of neuronal cultures derived from human induced pluripotent stem cells (hIPSCs) obtained from healthy subjects as well as from patients. For our research we combine molecular, neuroanatomical, electrophysiological in vitro techniques (from single cell patch clamp over paired recordings to multielectrode array recordings) in order to reveal the link between gene and neuronal network phenotypes. Internships will be fully integrated in this interdisciplinary research.

Our group does research on chromatin and the relation between chromatin structure and transcription, DNA replication, recombination and repair. Research focuses on transcription factors, histone modifications and on SNF2-type ATPase bearing chromatin motors. With the aim to uncover how the chromatin structure affects the accessibility of the DNA and how it influences the proper functioning of our cells.

How did the first cell form? In the Soft Interfaces group, we aim to understand how a complex system like a living cell could have emerged from simple organic molecules. By self-assembly of peptides, nucleotides and sugars into liquid coacervate droplets, we make synthetic organelles that grow, fuse, split, and act as microreactors for chemical reactions. Many living cells still bear marks of these coacervate droplets in the form of membraneless organelles. In this case, we use a biophysical chemistry approach to investigate what their function is in cell organization.

In Martijn Huynen's group at the CMBI we exploit molecular 'omics data to predict the function of proteins, their interaction in complexes and pathways and their evolution. We focus on biomedically relevant systems like Plasmodium, the mitochondrion and the immune system. We develop methods for 'omics data analysis and collaborate with experimental groups to analyze their data.
We offer internships in the analysis of molecular 'omics data for students with a MLS, Bio, or Medical Biology background. Doing of the course MOL074, Comparative Genomics is highly recommended to an in internship, but can also be done as part of the internship.

Our group focuses on developing tools and mathematical models to understand the connections between gene expression, metabolism, and how cells function in both healthy and diseased states. We take a "vertical" approach, which means we aim to build a comprehensive model of cell behaviour at the molecular level. This model would allow us to simulate different cellular states and predict new strategies for treating diseases that may not have been obvious before. These predictions can then be tested in experiments.

The Computational Cell Fate group employs theoretical and computational tools to understand how cell fate (i.e., decisions about the future state of a cell) is regulated in development and disease through cell-to-cell and cell-environment interactions. In the contemporary scientific landscape, novel computational tools are key to extract deeper insight from increasingly complex experimental datasets. Our research group addresses this challenge by integrating physics/mathematics with deep learning to extract interpretable causal mechanisms from high dimensional single cell data. We use these models to investigate fundamental questions about cell behavior including 1) How do cells convert noisy signals from their surrounding environment into robust decisions? and 2) How is information relayed across spatial scales from genes to cells and to tissues through multilayered regulatory networks? We collaborate with other group at RIMLS and internationally to validate and apply these predictions to multiple biological contexts including developmental trajectories and cancer progression. 

We have opportunities for both bioinformatics/data analysis projects and model development projects.

Our group develops and utilizes different detection techniques based on laser spectroscopy and (real-time) mass spectrometry for monitoring volatile compounds. We perform research in a broad range of applications, from environmental to analysis of biomarkers in human breath. Some of the projects are in collaboration with colleagues from other departments and/or the academic hospital. We can host physics, science, chemistry, biomedical or molecular life science internships.
Non-invasive detection of biomarkers in human breath: we develop new methodologies to detect and monitor biochemical processes in the human body via untargeted and targeted biomarkers in exhaled breath. We combine multivariate analysis tools to relate them to health (diet, exercise, exposure) and diseased status (cancer, infections, etc.).
Sniffing the chemical language of pathogens:We analyze volatile metabolites produced by pathogens as infection-specific biomarkers.
Plasma diagnostics using spectroscopy: We design, develop and utilize a broadband absorption spectrometer for analyzing discharge plasmas. It is an applied research in the lab, well balanced between physics and chemistry combined with computational modeling and simulation.
Please check our website and fell free to contact us for more information on current projects and internships.

Our team pioneered and explored a 2D cell model to study genome regulation during early mouse embryogenesis, uncovering epigenetic mechanisms that drive Inner Cell Mass (ICM) cells to further develop. To refine our model and gain insight into implantation, we characterised new mouse pluripotent stem cells representing peri-implantation stages. We are currently building on these findings, including studying X inactivation in female PSCs. In addition, we established a network of material scientists and synthetic- and computational biologists to initiate single-cell -omics studies on cellular interplay within complex post-implantation 3D models (gastruloids). Recently we initiated a new research line on pre-implantation human embryogenesis. Within this research line, we focus on the effect of the embryo sex on embryogenesis, as well an on how human embryos cope with aneuploidies that regularly occur. Among others, such insights underlie further improvement of in vitro fertilization, in which the pre-implantation human embryos obtained often contain aneuploidies.

Our group uses a combination of single-cell genomics and microscopy methods to study the role of chromatin and epigenetics in gene-regulation control, with a focus on early mouse embryonic development and tumorigenesis. The aim of the lab is to understand the principles governing cellular decision-making. We are interested in how cells acquire new identities and traits in lineage specification events in mice and in cancer. To this end we employ and continuously develop novel single-cell technologies to delineate these processes with high sensitivity and accuracy.

At the Donders institute there are 4 main research themes. Within those themes there are several research departments active and some also have an overlap between the themes. You can find an overview of all departments through the website link. Please take your time to see what possibilities the departments offer and what their research is focusing on. 

At the Donders Institute there is also a section on talent development, which provide more information for future graduate students. On the webpage you can also find a list of contact persons, who you can address for additional information and questions.

• Start 6-9 months in advance.

• How will the internship fit in your personal planning. 

• What is your motivation to do the internship at that department. 

• What are your relevant qualifications (techniques and knowledge base)

• What would you like to learn.

The Donders Centre for Neuroscience is part of the Donders institute and the Faculty of Science. More information on education and internships can be found here.

https://www.ru.nl/en/donders-centre-for-neuroscience

Our group studies molecular mechanisms underlying stem cell differentiation and heart development, focusing on the dynamic changes in heart cells across the different time spans of embryonic development, adult life (disease), and evolution. The group examines heart development in different species and human stem cell-based models to understand fundamental principles of developmental competence and self-organisation, and the relationship between evolution and development. Deep conservation and differences among species are equally instructive to understand the heart better. With clinical partners, we also study tissue remodelling in human heart disease. By studying chromatin, gene regulation, and single cell trajectories, we aim to uncover fundamental biological principles and discover new avenues for treating disease and advancing regenerative medicine.

Our research group studies how metabolism influences epigenetic regulation and chromatin structure. Our work focuses on how metabolic pathways generate molecules that modify histones and affect gene expression. Using biochemical, proteomic, and genomic approaches, the lab investigates how these metabolic signals regulate chromatin during development and disease. A major goal is to understand how metabolic states reshape the epigenetic landscape of cells. This research helps reveal links between metabolism, chromatin regulation, and human health.

Our group is exploring the biology of malaria parasites and their delicate interaction with the human host. We integrate (single-cell) multi-omic, bioinformatic, biochemical and genetic engineering approaches to identify key gene regulatory mechanisms that enable the parasite to develop and adapt to its host environment. These studies provide molecular insights into regulatory processes essential for the parasite survival and hence critical knowledge for the development of improved intervention strategies.

The Life Science Trace Detection Laboratory (TDLab) focuses on reliable detection and quantification of volatile compounds in complex gas mixtures. We develop and apply techniques and analytical methodologies using state-of-the-art mid-infrared laser-based spectroscopy (e.g. with broadband supercontinuum sources and custom-made Fourier transform spectrometers) and high-resolution mass spectrometry (e.g. PTR-ToF-MS) for a wide range of gas concentrations (from sub ppb level to ppm and percentages).

We aim to develop gas sensing systems that can be deployed in the field for various applications, such as biomarkers detection for precision medicine, fruit quality monitoring, dairy farming, air quality monitoring, process control, plasma diagnostics, etc. Our lab is also open to external parties for analysis using our state-of-the-art instrumentation.

The group is part of the Department of Spectroscopy and Catalysis within the Institute for Molecules and Materials (IMM), bridging chemistry and instrumental physics. We participate in the IMM research themes Structure and Dynamics of Molecules and Chemistry of Complex Systems

Turning supramolecular chemistry into life-like materials. 

We build chemical systems that combine molecular self-assembly and chemical reactions in fascinating life-like behaviour such as growth, shape transformation, chemotaxis and signal transfer.

 
Currently, we are developing self-assemblies that organize themselves into wire-like structures – in a (primitive) analogy to the growth of slime mold wires. We aim to use these wires to grow a “chemical computer”, where the self-assembled wires “guide” either molecular or electric signals. Ultimately, we envision to use these wires in self-organizing device interfaces that “determine” the path of samples in lab-on-a-chip applications, or neuromorphic electronics that adapt upon growing new connections in the circuit (in analogy to neurons in the brain).

Our research involves a wide diversity of techniques and approaches, such as supramolecular chemistry, systems chemistry, synthesis, electrochemistry, microscopy, spectroscopy, building devices via 3D printing, automated image analysis, etc.

 
Currently, we have internship projects available on:
- Combining enzymatic reactions and self-assembly for chemical signal transfer along wires.
- Building and programming robotic devices to control the self-organization of our dynamic wire networks.
- Using electrochemistry for controlled assembly of dynamic, conductive connections in neuromorphic circuits.
- Design and synthesis of molecular building blocks for new concepts in out-of-equilibrium self-assembly to control the growth of the networks.

Depending on your preferences, we will design a project that suits your interest and background. For more info on our research and contact details, please check out our new website: www.korevaarlab.com.

“The Max Planck Institute has been at the forefront of interdisciplinary research into the foundations of language and communication. Our approach to the science of language and communication is unique because we address these fundamental issues at multiple levels, from molecules and cells, to circuits and brains, all the way through to the behaviour of individuals and populations.” 

The MPI offers internship possibilities which can be found via their website or directly use the link below. These vacancies include information for contact and application. Please check the vacancy page regularly.

You can also browse the research departments and try to contact the corresponding PI. However, it is encouraged that you seek a way for personal contact. Perhaps you know lecturers, from the MPI, from a course or lecturers who collaborate with MPI who you can address face to face.

https://www.mpi.nl/page/research-groups

https://www.mpi.nl/career-education/vacancies

Our group is studying abnormal proteins called oncoproteins and their role in blood cancer development using various next generation sequencing and proteomics approaches. Understanding the binding regions of these proteins, the effects on gene activity, and the associated epigenetic features can provide valuable information about the underlying mechanisms of leukemia and potentially lead to the development of targeted therapies or diagnostic tools.

Life is supported by fibrous hydrogels: they are present inside our cells (cytoskeleton) and between them (extracellular matrix). Synthetic gels, typically have very different properties than gels of biological materials, such as actin, fibrin and collagen, and, therefore are often unsuited for biomedical applications.

In the Molecular Materials group, we develop synthetic materials that do behave like biological hydrogels. The research in our group follows two lines: gel design, e.g. a gel that becomes 10-fold stiffer by heating 1 °C and biological application of the gel, for instance as an advanced cell culture medium or even for medical applications.

For internships, we host students from Chemistry and Science (most often in gel design, analysis and modelling) as well as students from Molecular Life Sciences and Medical Biology (for biomedical studies and cell biology).

CURRENTLY, WE ARE LOOKING FOR STUDENTS FOR CELL CULTURE APPLICATIONS. Interested, shoot us an email: p.kouwer@science.ru.nl

Molecular machines and motors in metal-based catalysis

Inspired by the complex working mechanisms of natural enzymes and biological motors and machines, our group develops supramolecular systems that can act as catalysts to convert (polymeric) substrates into desired products with a high level of control.

In particular, we aim at developing a new technology to write, store, and read information onto molecules, i.e. on single polymer chains, with the help of molecular machines that are inspired by the Turing machine, hypothetical device proposed by the British mathematician Alan Turing in 1936 as the general basis for the operation of a computer. Data storage on polymer chains is highly relevant nowadays as it may help solve the problem of handling the exponential growth of information that is currently trafficking the internet. Moreover, molecular data storage is expected to cost orders of magnitude less energy than conventional data storage in large data centers, making it a sustainable research target.

The group is working on the encoding of digital information into single polymer molecules in the form of chemical groups, such as (R,R)- and (S,S)-epoxides or (R)- and (S)-sulfoxides, which represent the digits 0 and 1. These are imprinted with the help of light-switchable catalytic machines that threads onto a polymer chain containing alkene double bonds or aryl sulfides. While moving along the chain the catalytic machines (ep)oxidize these functional groups (Figure). The enantioselectivity of the oxidation reactions is controlled by metal-containing catalysts of which the chirality can be switched by an attached Feringa-type molecular motor.

The research involves the synthesis of chiral cage compounds, light-switchable metal-containing catalysts and polymers, and the study of their properties with various techniques (NMR, IR, circular dichroism, UV-vis, fluorescence), threading experiments, and catalysis experiments, all focused on the writing of information.

Antibiotic resistance is a major problem in medicine and poses a threat to global human health. To better understand the molecular processes underlying resistance and ultimately find a solution to this problem we synthesize and apply small molecule tools. We use multistep organic synthesis to develop fluorogenic substrates for key enzymes involved in the emergence of resistance and apply them to live cells to unravel the molecular mechanisms that lead up to resistance. Furthermore, we have a special interest in the roles of nucleic acids (RNA and DNA) in the development of antibiotic resistance. We synthesize potential antibiotic molecules that target these nucleic acids in bacteria. Ultimately, we use our findings to device new molecular strategies to combat the antibiotic crisis.

The ultimate aim of our research is to understand how life works and where it comes from. Research in our group is multidisciplinary and exploits microfluidic tools to create synthetic cells or to study complex reaction networkss. We have a strong interest in complex molecular systems and study how networks of chemical reactions create functional behavior like oscillations, switches or amplifiers. In effect, we try and construct molecular computers. In your internship you will have the opportunity to combine robotics, AI and high throughput experiments.

Our laboratory focuses on epigenetics and chromatin regulation during cell differentiation. Our group develops advanced proteomics and genomics technologies to study how proteins interact with chromatin and RNA. Our work identifies chromatin-binding factors and histone modifications that control gene expression programs. We also investigate how these regulatory networks change during development and disease. Our research provides insight into how epigenetic mechanisms control cellular identity, as well as how this regulation is disrupted in cancer cells.

At the Radboudumc there are over 40 science or medically driven research departments. You can find an overview of all departments through the website link.

Please take your time to see what possibilities the departments offer and what their research is focusing on. Most departments have a paragraph dedicated on the application for an internship. At the Radboudumc most internships have a duration of at least 10 weeks.

It is encouraged that you seek a way for personal contact (face-to-face). The best way is to contact lecturers from course directly after a lecture. Alternatively, you can ask lecturers who collaborate with the departments at the Radboudumc. 

To smoother the application process, prepare yourself: 

• Start 6-9 months in advance.
• How will the internship fit in your personal planning. 
• What is your motivation to do the internship at that department. 
• What are your relevant qualifications (techniques and knowledge base)
• What would you like to learn.

Are you excited about research at the interface of materials, chemistry, biology and medicine? We are a multidisciplinary and international group with diverse scientific and clinical backgrounds. We strive to:

1. understand and control fundamental materials properties that can be translated into more effective regenerative therapies.
2. design molecular and particulate building blocks and control their assembly into tunable biomaterial platforms.
3. exploit biofabrication principles for engineering of complex tissues.

Interested to learn more about current projects? Shoot us an email at mani.diba@radboudumc.nl

Regulation of transcription (copying of a gene’s DNA) is essential for the normal growth and function of cells. In a single cell, transcription can show large fluctuations in activity over time, resulting in variability between cells in a population. Such variability can result in different cellular responses of individual cells, for example to drug treatment. Our lab uses and develops single-molecule imaging techniques to visualize individual protein and RNA molecules in living cells. Our goal is to understand the regulatory mechanisms and dynamics of transcription in single cells.

The Roithová group is studying and designing metal complexes to mediate efficient chemical transformations. We seek inspiration from enzymes that can make reactions selective and can use abundant reactants such as oxygen or CO2. By researching working principles of enzyme-inspired catalysts and by coupling these catalysts with photochemistry and electrochemistry we aim to develop more efficient chemical transformations and thereby to contribute to reducing the environmental impact of chemistry in the future.

Our group focuses on elucidating the fundamental mechanisms underlying stem cell fate determination, proliferation and differentiation, which are pivotal to human development and diseases pathology. Leveraging systems biology methodologies, including (single-cell) multi-omics and computational integrative analyses, we investigate gene regulation in human stem cells and derived organotypic models, in both healthy and diseased states. Through these studies, we uncover fundamental insights into the regulatory circuitry and mechanisms in stem cells, and offer powerful and effective tools for tissue regeneration and therapeutic intervention. We currently focus on investigating cell fate control mechanisms of human epithelial stem cells, their derived in vitro model models and their translational potential including drug discovery and tissue regeneration. We apply (single-cell) multi-omics and computational integrative analyses on human pluripotent stem cells and adult stem cells, to identify key transcription factors that drive cell fates and their regulatory mechanisms in the epigenetic and the chromatin landscape.  These studies provide molecular insights into cell differentiation, normal development and disease mechanisms. With these insights, we manipulate the cell fates for cell therapy and tissue regeneration, and identify therapeutic strategies.

Our structural bioinformatics group at the CMBI is led by Li Xue and Hanka Venselaar. Our research interests focus on bridging artificial intelligence (AI) and structural biology to better understand the molecular basis of diseases and to rationalize drug design. We use information obtained from available structures, homology models, and other data-sources in order to, for example, interpret variations, improve experimental design, drug docking, etc.
One of our main projects focusses on developing AI methods for better cancer vaccine design. A combination of Deep Learning and Integrative Modelling is used to predict MHC-peptide-T cell receptor complexes. We welcome talented students to join our endeavor.
We offer internships for Chem/MLS/Biol students (both Ma and Ba) either with a clear interest and understanding of protein folding or with an enthusiasm of AI.
An internship without programming experience is possible in the field of 3D modelling and mutant analysis. The AI project requires at least a decent basic level of programming skills. Internships, also in collaboration with other departments, are possible in many different fields.

The Rutjes group focuses on the development of new synthetic methodology, mainly focused on the synthesis of small organic molecules with specific biological activity. This includes projects on chemical reactions in continuous (photochemical) microreactors, medicinal chemistry projects to prepare lead compounds for specific drug targets, and asymmetric synthesis methods to prepare enantiopure products.

In nature, countless complex structures are known, and mimicking these structures can be a challenging task. How do you design a nano- or micro-system from the bottom up? Our goal is to design functional supramolecular structures and apply them to advance the field of nanomedicine.

Our group finds their inspiration in natural materials and processes. It is our aim to develop functional polymers, peptide and protein-based hybrid materials with biological activity. By using a variety of synthetic techniques, such as controlled polymerization, peptide synthesis and protein engineering methods. We furthermore mimic natural biological processes by compartmentalization and assembly of biocatalysts in polymeric capsules (polymersomes) for the design of synthetic mobile systems.