Molecular mechanism sheds light on neurodegenerative diseases

Alzheimer's, Parkinson's, Lou Gehrig's - Huntington's. These neurodegenerative diseases exhibit loss of nerve function in
different ways, from memory lapses to uncontrollable muscular movements, but it is now believed that these diseases share
many common molecular mechanisms.


A team of Northwestern University scientists, led by Richard I. Morimoto, John Evans Professor of Biology, has made a key
discovery toward understanding one of these mechanisms. In studying toxic proteins involved in Huntington's disease, they
discovered that the disease-causing protein severely interferes with the working of the proteasome, the cellular machine
responsible for eliminating damaged proteins within the cell.


The findings, which could lead to an understanding of how to prevent neurodegenerative diseases and to the development of
effective drugs, will be published Oct. 27 in The EMBO Journal, a publication of the European Molecular Biology Organization.



The proteasome is responsible for cell homeostasis. In healthy cells, proteins perform their function and then, with the help
of the proteasome, disappear. If idle and damaged proteins remain, their presence can affect cell behavior.



Misfolded and damaged proteins are common to all human neurodegenerative diseases. They clump together to form toxic
aggregates that destroy cell function and cause disease. Morimoto's team is the first to demonstrate in living human cells
and in real time that the toxic protein aggregates, in this case caused by mutant Huntingtin, bind to the proteasome machine
irreversibly and prevent the complete degradation of the proteins. This evidence could help explain the disease process.



"We believe this suggests why Huntington's disease is so destructive," said Morimoto. "Once bound, the toxic proteins do not
release the proteasome. This interference with the normal clearance of proteins has a cumulative and amplifying negative
effect. The proteins that are normally degraded build up."



The researchers' data also show that the toxic proteins and proteasome are bound together in a close and stable fashion,
indicating that the proteins are trapped within the proteasome. This could explain the negative consequences on the health of
the cell in which disease builds over decades before symptoms result.



In addition to Morimoto, other authors on the EMBO paper are Carina I. Holmberg, a post-doctoral fellow and the paper's lead
author; Kwame N. Mensah, a graduate student; and Andreas Matouschek, associate professor of biochemistry, molecular biology
and cell biology, from Northwestern University; and Kristine E. Staniszweski, a former graduate student at Northwestern.



The research was supported by the National Institutes of Health, the Huntington Disease Society of America Coalition for the
Cure and the Daniel F. and Ada L. Rice Foundation.


Contact: Megan Fellman

fellmannorthwestern

847-491-3115

Northwestern University