| Literature DB >> 19491400 |
Justin Legleiter1, Gregor P Lotz, Jason Miller, Jan Ko, Cheping Ng, Geneva L Williams, Steve Finkbeiner, Paul H Patterson, Paul J Muchowski.
Abstract
Huntington disease (HD) is a neurodegenerative disorder caused by an expansion of a polyglutamine (polyQ) domain in the N-terminal region of huntingtin (htt). PolyQ expansion above 35-40 results in disease associated with htt aggregation into inclusion bodies. It has been hypothesized that expanded polyQ domains adopt multiple potentially toxic conformations that belong to different aggregation pathways. Here, we used atomic force microscopy to analyze the effect of a panel of anti-htt antibodies (MW1-MW5, MW7, MW8, and 3B5H10) on aggregate formation and the stability of a mutant htt-exon1 fragment. Two antibodies, MW7 (polyproline-specific) and 3B5H10 (polyQ-specific), completely inhibited fibril formation and disaggregated preformed fibrils, whereas other polyQ-specific antibodies had widely varying effects on aggregation. These results suggest that expanded polyQ domains adopt multiple conformations in solution that can be readily distinguished by monoclonal antibodies, which has important implications for understanding the structural basis for polyQ toxicity and the development of intrabody-based therapeutics for HD.Entities:
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Year: 2009 PMID: 19491400 PMCID: PMC2755888 DOI: 10.1074/jbc.M109.016923
Source DB: PubMed Journal: J Biol Chem ISSN: 0021-9258 Impact factor: 5.157