A PROTEOMICS APPROACH
TOWARD THE UNDERSTANDING OF SCHIZOPHRENIA AND BIPOLAR DISORDER
J.E.
Swatton1, P. Sudhakaran1, N.A. Karp2, S. Hester2,
N.D. and S. Bahn1,3
1Department of
Neurobiology, Babraham Institute, Cambridge CB2 4AT, UK; 2Department
of Biochemistry, Cambridge Centre for Proteomics, University of Cambridge,
Cambridge, CB2 1QW, UK; 3Department of Psychiatry, University of
Cambridge, Addenbrooke’s Hospital, Cambridge CB2 2QQ, UK
Schizophrenia and bipolar disorder each affect ~1% of the population worldwide,
but despite such high incidences, the aetiology of both disorders remains
elusive. We have employed the latest advance in 2-D PAGE technology to
investigate protein expression changes for schizophrenia and bipolar disorder
compared with matched controls. Fresh-frozen pre-frontal cortex from white and
grey matter of 10 control and schizophrenia or bipolar disorder individuals was
subjected to a 2D-florescence differential gel electrophoresis (2-D DIGE) and
protein expression was quantified using Biological Variation Analysis software
(Amersham). Proteins of interest were excised from a Coomassie-stained gel, and
identified by Nanospray/LC-MS/MS. We identified abnormalities in the expression
of proteins involved in protein trafficking, the cytoskeleton, myelination and
energy metabolism in schizophrenia individuals. Preliminary results from an
analogous study on bipolar disorder have already highlighted some interesting
differences in protein expression for bipolar disorder compared with
schizophrenia.
This work was supported
through a centre grant by the Stanley Medical Research Institute