Lectures and seminars Opponent seminar - Professor Harm H. Kampinga
The role of the Hsp70-regulator DNAJB6 in cellular protein homeostasis: relevance to neuro and muscular degenerative disease.
Welcome to a seminar with Professor Harm H. Kampinga from University of Groningen
Title: "The role of the Hsp70-regulator DNAJB6 in cellular protein homeostasis: relevance to neuro and muscular degenerative disease.".
Time: Thursday October 27th at 3pm.
Place: Room D1012, Level 10, Biomedicum, Karolinska Institutet, Solna
Speaker: Professor Harm H. Kampinga from Department of Biomedical Sciences of Cells & Systems, University of Groningen, The Netherlands. The opponent in Shanshan Xu's dissertation.
Harm Kampinga graduated in Biology at the University of Groningen in 1984 and received his PhD in 1989 in Groningen. After being assistant – and associated professor in Radiation Oncology, he became full professor in the Department of Cell Biology in 2001 and became head of this Department in 2015.The central theme of his research has always been related to the consequences of protein un- or misfolding on cellular functions. Initially, his work was centered around the biological effects of heat shock on cells in relation to the use of hyperthermia in combination with radiation or/and chemotherapy in cancer treatments. During these studies, Kampinga became interested in Heat Shock Proteins (HSP) that could protect cells from the cell biological effects of heat shock and focused his research on the functional regulation and diversity HSPs.
Kampinga’ s lab was the first to clone a majority of all human and Drosophila HSPs and subsequently screened them for activity in several (age-related) cell and drosophila models for neurodegenerative diseases (in particular CAG repeat expansion diseases) and cardiac diseases. Major discoveries from his lab include the asymmetric segregation of protein damage in stem cells, the functional diversity of HSPs and their role in dealing with different disease-associated protein aggregation diseases, and the discovery of set of specific DNAJ family protein members (DNAJB6 and DNAJB8) with an exquisitely high potency to delay amyloidogenesis.