Proteomics & Mammalian Cell Biology Section
The Proteomics & Mammalian Cell Biology Section functions as a core facility for cancer proteomics at The Norwegian Radium Hospital. Furnished with a nano-LC interfaced ESI ion trap mass spectrometer with ETD capabilities as well as a MALDI-TOF mass spectrometer the section explores the possibility of using large-scale proteomic analysis as a cancer diagnostic tool. Additional expertise includes instrumentation devoted to multi-dimensional protein separation based on gel- and non-gel applications. In conjunction with Core Facility for Proteomics at OUS/Gaustad, the section provides proteomic service and project collaboration with medical researchers and other scientists at Oslo University Hospital.
In the section's own research projects, proteomics is used to study autophagic protein degradation in normal and malignant liver cells, and the role of phosphorylation-based signalling pathways (in particular the stress-activated AMPK pathway) in the regulation of autophagy, apoptosis (programmed cell death), and cytoskeletal organization.
In the section's own research projects, proteomics is used to study autophagic protein degradation in normal and malignant liver cells, and the role of phosphorylation-based signalling pathways (in particular the stress-activated AMPK pathway) in the regulation of autophagy, apoptosis (programmed cell death), and cytoskeletal organization.
Contact information:
Department of Cell Biology, Institute for Cancer Research,
The Norwegian Radium Hospital, Montebello, N-0310 Oslo, Norway
Email Per.O.Seglen@rr-research.no, Phone:+47 22 78 19 80, Fax: +47 22 78 19 95
Department of Cell Biology, Institute for Cancer Research,
The Norwegian Radium Hospital, Montebello, N-0310 Oslo, Norway
Email Per.O.Seglen@rr-research.no, Phone:+47 22 78 19 80, Fax: +47 22 78 19 95
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Latest articles
Per O. Seglen
Guidelines for the use and interpretation of assays for monitoring autophagy
Autophagy, 8 (4), 445-544
PubMed 22966490
Autophagic activity measured in whole rat hepatocytes as the accumulation of a novel BHMT fragment (p10), generated in amphisomes by the asparaginyl proteinase, legumain
Autophagy, 7 (9), 1011-27
PubMed 21610319
Seeing is believing: the impact of electron microscopy on autophagy research
Autophagy, 7 (9), 935-56
PubMed 21566462





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