The structural impact of a polyglutamine tract is location-dependent.
Ontology highlight
ABSTRACT: Polyglutamine (polyQ) expansion leads to protein aggregation and neurodegeneration in Huntington's disease and eight other inherited neurological conditions. Expansion of the polyQ tract beyond a threshold of 37 glutamines leads to the formation of toxic nuclear aggregates. This suggests that polyQ expansion causes a conformational change within the protein, the nature of which is unclear. There is a trend in the disease proteins that the polyQ tract is located external to but not within a structured domain. We have created a model polyQ protein in which the repeat location mimics the flexible environment of the polyQ tract in the disease proteins. Our model protein recapitulates the aggregation features observed with the clinical proteins and allows structural characterization. With the u
SUBMITTER: Robertson AL
PROVIDER: S-EPMC2599835 | biostudies-literature | 2008 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA