Accumulation of manganese in the cells disrupts protein transport leading to the hereditary parkinsonian syndrome. Scientists studied the genetic mutation that causes the disease, using X-ray fluorescence at synchrotrons DESY and ESRF.
Parkinsonian syndrome is a set of diseases with symptoms similar to Parkinson's disease. Some are caused by high quantities of manganese, a metal essential to the body at trace levels. This is especially so for a hereditary form of the disease caused by a genetic mutation responsible for a toxic accumulation of manganese in cells.
The team of researchers has shown a key mechanism for the disease caused by this mutation. At the DESY synchrotron (Hamburg, Germany), they have been able to locate manganese inside individual cells, (1) using the fluorescent signature it produces under an X-ray beam. Manganese concentrates essentially in the Golgi apparatus, a cellular compartment which acts as a dispatch center for proteins. The proteins receive a label and are accordingly packaged within vesicles to other compartments, or to the outside of the cell. It is in these vesicles--barely 50 nm in diameter--that manganese accumulates, as the researchers have demonstrated by repeating their experiments in the ESRF synchrotron (The European synchrotron, Grenoble), with even higher sensitivity and spatial resolution. This is the only place in the world where the equipment's spatial resolution and sensitivity were sufficient to detect the minute amounts of manganese in the vesicles.