2 Doctoral Candidate Positions in Cell Biology
Horizon Europe-funded Marie Skłodowska-Curie Action (MSCA) doctoral network
Horizon Europe-funded Marie Skłodowska-Curie Action (MSCA) doctoral network
Systasy Bioscience GmbH, a Munich-based biotech company, uses advanced barcoding technologies and next-generation disease modeling to facilitate drug discovery in complex diseases. Systasy’s innovative and proprietary technologies provide a fast and cost-effective approach to mapping disease pathways from the cellular level to the patient cohort level to enable next-generation medicine. Systasy’s barcoding technology uses molecular barcodes to track different entities within one experiment. These entities include activities of targets and cellular pathways, cell types and patient material, as well as technical features such as biological replicates, wells, and plates. When applied to next-generation stem cell-derived disease models, Systasy’s barcoded and cell-based profiling assays enable multiplexed and scalable drug screening in early-stage drug discovery.
Systasy Bioscience GmbH is pleased to announce that two PhD positions will be available from 1 January 2024 or as soon as possible thereafter. The application deadline is 1st November 2023.
Applications are invited for the three-year fellowship from applicants who hold or expect to hold a master´s degree in a field relevant to the following PhD projects. Successful applicants will be enrolled in the Munich Medical Research School of the LMU Munich, Germany.
Employer: Systasy Bioscience GmbH | Location: Munich, Germany
Research Field: Biological sciences » Biology »Neuroscience » Neurobiology
Application Deadline: 1st November 2023 | Education Level: Master Degree or equivalent
We are looking for two driven and ambitious persons, with an ability to work independently and in collaboration with other research groups. The candidates should have a strong interest in pursuing a PhD degree in the field of cell biology with a focus on intrinsically disordered proteins (IDPs).
The positions are part of the Horizon Europe-funded Marie Skłodowska-Curie Action (MSCA) doctoral network called IDPro, which focuses on Intrinsically Disordered Proteins in Health and Disease: Mechanisms, Molecular Context and Opportunities for Drug Discovery. IDPro is an exceptional network of nine beneficiaries (eight academic and one industrial) and five partner organizations (four industrial and three academic) from seven different countries, with excellent track records in protein research and supervision. Together, we will train eleven doctoral candidates, with distinct competencies of relevance for the field of intrinsically disordered proteins, to secure future scientific breakthroughs in a rapidly developing field. In particular, we will investigate how disordered proteins interact, how interaction is affected by disease-related mutations, and assess how disordered proteins cause aberrant cellular signaling in relevant human disease models. Furthermore, we will design ligands that can be further developed into molecular probes, which could represent lead structures for the development of drugs. The goal of IDPro is to strengthen an emerging field in biology and medicine with implications for both academia and industry in the European union.
In Project 1, the PhD candidate will establish an array of cell-based assays for IDPs in human cell lines. Assays will use Systasy’s splitSENSOR (in the literature also known as split TEV) and EXTassay barcoding technologies to enable a multiplexed readout to assess both the association to key interaction partners and the effect on physiological signaling pathways. splitSENSOR and EXTassay barcoding technologies are established at our site and were combined in a so-called targetProfiler approach before (see Galinski et al., 2018, Sci Reports as reference). Examples of IDPs to be selected are, but not limited to, amyloid precursor protein (APP), γ-secretase/presenilin, a-synuclein, and calmodulin kinase II. Furthermore, the candidate will profile interactions for selectivity and specificity, and will assess IDP-directed antagonists in these assays.
In Project 2, the PhD candidate will establish an array of validated CRISPR mediated genetic perturbation tools to assess a gain- and loss-of-function analysis of IDP interactions that are relevant to the regulation of neuronal signaling and cell fate. To do this, the PhD candidate will e.g., apply CRISPR inhibition (or knockout) directed on IDP candidates in a human disease model and combine this technique with a multi-pathway profiling assay (using company-owned barcoded pathwayProfiler assay, see Herholt et al., 2018, Sci Reports as reference) to identify affected targets and pathways (e.g., including cell fate, cell stress, immune signaling, metabolism, pluripotency, neuronal signaling). Data obtained from the pathway profiling will be complemented by (single cell) RNA-seq analyses.
The position is available for a three-year period for applicants holding a relevant master´s degree.
To be eligible, the candidate must
Preferred Qualifications
We are looking for highly motivated individuals with a background in cell biology and molecular biology, ideally with some experience in R language, pharmacology and/or molecular cloning.
General job Description
Your main responsabilities as a PhD fellow at Systasy Bioscience GmbH will be to:
For further information, applicants may contact the supervisor PD Dr. Michael Wehr (wehr@systasy.de), co-founder and chief technical officer (CTO) of Systasy Bioscience GmbH, Munich, Germany, and Head of Research Group Cell Signalling, Department of Psychiatry and Psychotherapy, LMU Munich, Germany.
Applicants are requested to submit their application electronically via E-Mail to jobs@systasy.de (combined in one pdf file) including:
Deadline for applications:
1st November 2023. Please note that only online applications will be accepted.
Systasy Bioscience GmbH would like to encourage everyone interested in this position to apply, regardless of their personal background.
Download this page: Job opportunities @Systasy
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