
Do you want to find out why dopamine neurons die in Parkinson's disease – and how to stop it?

Do you want to find out why dopamine neurons die in Parkinson's disease – and how to stop it?
We are looking for an enthusiastic PhD candidate for a project on the ubiquitin-dependent control of neuronal survival in Parkinson's disease (PD). Neurons in the substantia nigra pars compacta are selectively lost as PD progresses. Our work on the BCL2 protein family has identified MCL1 as a weak link in the survival of these neurons: it is a short-lived protein whose level is set by ubiquitin-dependent degradation and by its antagonist NOXA. Do you want to find out which enzymes set that balance, and whether they can be used to keep dopamine neurons alive? Then this project is for you.
We welcome applications from candidates with diverse backgrounds, experiences and perspectives. If you recognise yourself in the role but do not meet every listed preference, we encourage you to apply.

We are looking for an enthusiastic PhD candidate for a project on the ubiquitin-dependent control of neuronal survival in Parkinson's disease (PD). Neurons in the substantia nigra pars compacta are selectively lost as PD progresses. Our work on the BCL2 protein family has identified MCL1 as a weak link in the survival of these neurons: it is a short-lived protein whose level is set by ubiquitin-dependent degradation and by its antagonist NOXA. Do you want to find out which enzymes set that balance, and whether they can be used to keep dopamine neurons alive? Then this project is for you.
We welcome applications from candidates with diverse backgrounds, experiences and perspectives. If you recognise yourself in the role but do not meet every listed preference, we encourage you to apply.
You will identify the E3 ubiquitin ligases and deubiquitinating enzymes (DUBs) that control MCL1 and NOXA turnover in dopaminergic neurons, and determine what happens to neuronal survival when you manipulate them.
The backbone of the project is interaction proteomics: you will perform (co-) immunoprecipitations from neuronal cell models and brain tissue followed by quantitative LC-MS/MS, and you will run that workflow from end to end – from sample preparation to data analysis and interpretation. Candidate regulators are then validated biochemically, in cellular and in vivo models of PD, and finally in human post-mortem midbrain tissue, so that you can connect a molecular mechanism to the disease itself.
You will work in a group that combines molecular neuroscience with proteomics and neuropathology, and you will have the room to shape the direction of your own project.
Tasks and responsibilities:
You enjoy hands-on experimental work, and you keep going when an experiment fails: you look for the reason rather than repeating it unchanged. You plan, so that long workflows such as a proteomics experiment are prepared well before the instrument time starts. You are precise in documenting what you do. You discuss your data critically in lab meetings, you ask for help when you need it, and you are a nice colleague in an interdisciplinary team of scientists.
Your experience and profile:
A temporary contract for 38 hours per week for the duration of 4 years (the initial contract will be for a period of 18 months and after satisfactory evaluation it will be extended for a total duration of 4 years). The preferred starting date is as soon as possible. This should lead to a dissertation (PhD thesis). We will draft an educational plan that includes attendance of courses and (international) meetings. We also expect you to assist in teaching undergraduates and master students.
The gross monthly salary, based on 38 hours per week, ranges from € 3,204 in the first year to € 4,051 in the fourth year of employment (scale P). This does not include 8% holiday allowance and 8.3% year-end allowance. The UFO profile Promovendus is applicable. A favourable tax agreement, the 30% ruling, may apply to non-Dutch applicants. The Collective Labour Agreement of Universities of the Netherlands is applicable.
Curious about our extensive secondary benefits package? You can read more about it here.
You will identify the E3 ubiquitin ligases and deubiquitinating enzymes (DUBs) that control MCL1 and NOXA turnover in dopaminergic neurons, and determine what happens to neuronal survival when you manipulate them.
The backbone of the project is interaction proteomics: you will perform (co-) immunoprecipitations from neuronal cell models and brain tissue followed by quantitative LC-MS/MS, and you will run that workflow from end to end – from sample preparation to data analysis and interpretation. Candidate regulators are then validated biochemically, in cellular and in vivo models of PD, and finally in human post-mortem midbrain tissue, so that you can connect a molecular mechanism to the disease itself.
You will work in a group that combines molecular neuroscience with proteomics and neuropathology, and you will have the room to shape the direction of your own project.
Tasks and responsibilities:
You enjoy hands-on experimental work, and you keep going when an experiment fails: you look for the reason rather than repeating it unchanged. You plan, so that long workflows such as a proteomics experiment are prepared well before the instrument time starts. You are precise in documenting what you do. You discuss your data critically in lab meetings, you ask for help when you need it, and you are a nice colleague in an interdisciplinary team of scientists.
Your experience and profile:
A temporary contract for 38 hours per week for the duration of 4 years (the initial contract will be for a period of 18 months and after satisfactory evaluation it will be extended for a total duration of 4 years). The preferred starting date is as soon as possible. This should lead to a dissertation (PhD thesis). We will draft an educational plan that includes attendance of courses and (international) meetings. We also expect you to assist in teaching undergraduates and master students.
The gross monthly salary, based on 38 hours per week, ranges from € 3,204 in the first year to € 4,051 in the fourth year of employment (scale P). This does not include 8% holiday allowance and 8.3% year-end allowance. The UFO profile Promovendus is applicable. A favourable tax agreement, the 30% ruling, may apply to non-Dutch applicants. The Collective Labour Agreement of Universities of the Netherlands is applicable.
Curious about our extensive secondary benefits package? You can read more about it here.
The Swammerdam Institute for Life Sciences is located at the vibrant Amsterdam Science Park. SILS is one of eight institutes of the University of Amsterdam's Faculty of Science (FNWI). With around 240 employees, SILS carries out internationally high-quality life science research and provides education within various university programmes. Research revolves around four main themes: Cell & Systems Biology, Neurosciences, Microbiology and Green Life Sciences.
You will be embedded in the Molecular Neuroscience group. The mission of the group is to understand the fundamental molecular processes that underlie neurodevelopment and neuronal function in health and disease, with a focus on the midbrain and, more recently, on the cell survival machinery of dopamine neurons in relation to PD. Dr. Lars van der Heide will act as your daily supervisor and Prof. dr. Marten Smidt as your promotor. For the validation in human post-mortem tissue, we collaborate with Dr. Anke Dijkstra and the Netherlands Brain Bank; the mass spectrometry work is carried out in collaboration with Dr. Gertjan Kramer.
The Swammerdam Institute for Life Sciences is located at the vibrant Amsterdam Science Park. SILS is one of eight institutes of the University of Amsterdam's Faculty of Science (FNWI). With around 240 employees, SILS carries out internationally high-quality life science research and provides education within various university programmes. Research revolves around four main themes: Cell & Systems Biology, Neurosciences, Microbiology and Green Life Sciences.
You will be embedded in the Molecular Neuroscience group. The mission of the group is to understand the fundamental molecular processes that underlie neurodevelopment and neuronal function in health and disease, with a focus on the midbrain and, more recently, on the cell survival machinery of dopamine neurons in relation to PD. Dr. Lars van der Heide will act as your daily supervisor and Prof. dr. Marten Smidt as your promotor. For the validation in human post-mortem tissue, we collaborate with Dr. Anke Dijkstra and the Netherlands Brain Bank; the mass spectrometry work is carried out in collaboration with Dr. Gertjan Kramer.
If you feel the profile fits you, and you are interested in the job, we look forward to receiving your application. You can apply online via the red button. We accept applications until and including 13 October 2026.
If you have any questions or do you require additional information? Please contact:
Applications should include the following information (all files besides your cv should be submitted in one single pdf file):
A knowledge security check can be part of the selection procedure.
(for details: national knowledge security guidelines)
If you feel the profile fits you, and you are interested in the job, we look forward to receiving your application. You can apply online via the red button. We accept applications until and including 13 October 2026.
If you have any questions or do you require additional information? Please contact:
Applications should include the following information (all files besides your cv should be submitted in one single pdf file):
A knowledge security check can be part of the selection procedure.
(for details: national knowledge security guidelines)

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