| Autor: |
Gao X; The C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26505, United States., Campbell WA 4th; Department of Chemistry, Gettysburg College, Gettysburg, Pennsylvania 17325, United States., Chaibva M; The C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26505, United States., Jain P; The C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26505, United States., Leslie AE; The C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26505, United States., Frey SL; Department of Chemistry, Gettysburg College, Gettysburg, Pennsylvania 17325, United States., Legleiter J; The C. Eugene Bennett Department of Chemistry, West Virginia University, Morgantown, West Virginia 26505, United States.; NanoSAFE, P.O. Box 6223, West Virginia University, Morgantown, West Virginia 26506, United States.; The Center for Neurosciences, West Virginia University, Morgantown, West Virginia 26505, United States. |
| Abstrakt: |
Huntington's disease (HD) is an inherited neurodegenerative disease caused by abnormally long CAG-repeats in the huntingtin gene that encode an expanded polyglutamine (polyQ) domain near the N-terminus of the huntingtin (htt) protein. Expanded polyQ domains are directly correlated to disease-related htt aggregation. Htt is found highly associated with a variety of cellular and subcellular membranes that are predominantly comprised of lipids. Since cholesterol homeostasis is altered in HD, we investigated how varying cholesterol content modifies the interactions between htt and lipid membranes. A combination of Langmuir trough monolayer techniques, vesicle permeability and binding assays, and in situ atomic force microscopy were used to directly monitor the interaction of a model, synthetic htt peptide and a full-length htt-exon1 recombinant protein with model membranes comprised of total brain lipid extract (TBLE) and varying amounts of exogenously added cholesterol. As the cholesterol content of the membrane increased, the extent of htt insertion decreased. Vesicles containing extra cholesterol were resistant to htt-induced permeabilization. Morphological and mechanical changes in the bilayer associated with exposure to htt were also drastically altered by the presence of cholesterol. Disrupted regions of pure TBLE bilayers were grainy in appearance and associated with a large number of globular aggregates. In contrast, morphological changes induced by htt in bilayers enriched in cholesterol were plateau-like with a smooth appearance. Collectively, these observations suggest that the presence and amount of cholesterol in lipid membranes play a critical role in htt binding and aggregation on lipid membranes. |
