Construction and interrogation of neural circuits with single cell resolution on high-density MEA chips.
What you will do
Neurodegenerative diseases such as Parkinson’s Disease cannot be studied in situ in a living patient, and the much-studied transgenic animal models have not demonstrated to deliver on their promise of bringing a cure. For many of these diseases, there is no or only symptomatic treatment available. Radically novel approaches are needed to shed new light on mechanisms and pathways behind these complex disorders.
We are building neural microcircuits on high-density CMOS microelectrode array chips that represent the affected brain circuit, by using the patient’s own cells. By single-cell electroporation using the chip’s electrodes, we introduce molecules to drive differentiation of stem or primary cells towards neuronal sub-types. The same electrodes are used to record electrophysiological (e-Phys) data from the neural circuit, thereby mapping novel phenotypes of disease. Additional assays are being developed with complementing cell types, such as astrocytes and microglia. The microcircuit model will be further developed and improved by moving from 2D to 3D cell assemblies. Finally, the e-Phys data will be complemented with transcriptome data and linked to the clinical background of the patient to improve the phenotype and stratify the patient population.
In this postdoc, your main activities will be:
– be actively involved in the creation and readout of the microcircuits
– handle stem cell cultures
– perform electroporation experiments, electrophysiology recording and data analysis
You will be working in a multidisciplinary and dynamic team. The project is part of Mission Lucidity2, a unique constellation of engineers, neuroscientists, and clinicians, with the aim to decode brain disease.
Vacancy and details: here.