Łukasiewicz PORT - Polish Center for Technology Development is a modern and dynamically developing Research Institute within the Łukasiewicz Research Network. It focuses on development of new technologies, resulting from basic and applied research which, in turn, serve as a basis for innovative solutions for the industry. The scientific branch of Łukasiewicz-PORT encompasses four Centers: Life Sciences and Biotechnology, Material Sciences, Population Diagnostics and the Independent Department P4Health, backed by specialized core facilities and excellent infrastructure that supports high quality research.
We are looking for an ambitious and passionate Postdoctoral fellow to join the research group of Dr Agnieszka Krzyżosiak in a project funded by the National Science Centre (NCN) OPUS 29 grant 2025/57/B/NZ5/04944 “Identification of age-related traces of Amyotrophic Lateral Sclerosis as a basis for the search for novel disease modifiers”. The position offers an exciting opportunity to contribute to a dedicated research team investigating key questions in neurodegeneration. A post-doc position is a full-time position planned by the project manager for a person who has obtained a doctoral degree in the year of employment in the project or in the 12 years prior to January 1st of the year of employment in the project.
Neurodegenerative diseases (NDDs) are devastating, age-related disorders that, despite substantial research efforts, remain largely incurable. Our work employs cutting-edge approaches to advance understanding of the molecular mechanisms of neurodegeneration, with the ultimate aim of proposing novel therapeutic strategies.
The deposition of misfolding-prone proteins is a hallmark of NDDs and consistent evidence points to the dysregulation of protein quality control (PQC) in neurodegenerative pathogenesis. We have previously demonstrated that boosting the PQC can be beneficial in preventing protein misfolding as well as ameliorating neurodegenerative phenotypes (Das, Krzyzosiak et al. 2015, Science; Krzyzosiak, Sigurdardottir et al. 2018, Cell). Building on these findings, our aim is to systematically investigate the molecular components of PQC pathways and to exploit their potential to modify NDD-associated cellular pathology. In parallel, we examine the contribution of glial cells to neurodegenerative disease progression.
In your role, you will use cell reprogramming methods and implement the state-of-the-art human model systems to investigate the origin and progression of the Amyotrophic Lateral Sclerosis pathology.