RUB researchers analyze proteome of cells
How abnormal protein deposits in the brains of Alzheimer's patients
disrupt the signalling between nerve cells has now been reported by
researchers in Bochum and Munich, led by Dr. Thorsten Müller from the
Medizinisches Proteom-Center of the Ruhr-Universität, in the journal
Molecular and Cellular Proteomics. They varied the amount of APP protein
and related proteins associated with Alzheimer's disease
in cell cultures, and then analysed how this manipulation affected
other proteins in the cell. The result: the amount of APP present was
related to the amount of an enzyme that is essential for the production
of neurotransmitters and therefore for communication amongst nerve
cells.
Proteomics: analysing all the proteins of the cells at once
Amyloid plaques are a characteristic feature of Alzheimer's disease.
They consist largely of cleavage products of the so-called amyloid
precursor protein APP, which occur in excess in the brains of
Alzheimer's patients. What role APP plays in healthy people and why the
abnormal accumulation of amyloid disrupts the regular functioning of the
brain is still largely unclear. To understand the function of APP, the
RUB researchers established a new cell model. The new cells produced
only a very small amount of APP. What impact this had on all the other
proteins of these cells was examined by the researchers through the use
of mass spectrometry, among other things. With this method they
identified over 2000 proteins and determined their concentrations. They
were looking specifically for molecules whose concentrations in the
newly established low-APP cells were different than in the reference
cells that contained normal amounts of APP.
Abnormal protein able to curb neurotransmitter production
"One candidate has particularly caught our attention, this being the
enzyme methionine adenosyltransferase II, alpha, MAT2A for short",
Thorsten Müller said. Among other things, the enzyme is crucially
involved in the production of neurotransmitters. Low-APP cells contained
less MAT2A than the reference cells. To confirm the connection between
the "Alzheimer's protein" APP and the neurotransmitter-producing MAT2A,
the team studied tissue samples from the brains of deceased Alzheimer's
patients and from healthy individuals. In the tissue of the Alzheimer's
patients there was less MAT2A than in the healthy samples. These results
suggest that APP and MAT2A concentrations are related and are linked to
the synthesis of neurotransmitters. "Our results point to a new
mechanism by which the defective cleavage of the APP protein in
Alzheimer's disease could be directly related to altered
neurotransmitter production", Müller said. "As a result, the signal
transduction of nerve cells could be disrupted, which, over an extended
period, could possibly also cause the death of cells."
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