Perturbation with Intrabodies Reveals That Calpain Cleavage Is Required for Degradation of Huntingtin Exon 1
Published 2011 View Full Article
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Title
Perturbation with Intrabodies Reveals That Calpain Cleavage Is Required for Degradation of Huntingtin Exon 1
Authors
Keywords
Lysosomes, Huntington disease, Proteases, Toxicity, Immunoprecipitation, Neurons, Calpain inhibitors, Phosphorylation
Journal
PLoS One
Volume 6, Issue 1, Pages e16676
Publisher
Public Library of Science (PLoS)
Online
2011-02-01
DOI
10.1371/journal.pone.0016676
References
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Related references
Note: Only part of the references are listed.- Antibody Therapy in Neurodegenerative Disease
- (2011) Amber L Southwell et al. REVIEWS IN THE NEUROSCIENCES
- Proteolysis of Mutant Huntingtin Produces an Exon 1 Fragment That Accumulates as an Aggregated Protein in Neuronal Nuclei in Huntington Disease
- (2010) Christian Landles et al. JOURNAL OF BIOLOGICAL CHEMISTRY
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- Mutant Huntingtin N-terminal Fragments of Specific Size Mediate Aggregation and Toxicity in Neuronal Cells
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- Phosphorylation of Threonine 3
- (2009) Charity T. Aiken et al. JOURNAL OF BIOLOGICAL CHEMISTRY
- IKK phosphorylates Huntingtin and targets it for degradation by the proteasome and lysosome
- (2009) Leslie Michels Thompson et al. JOURNAL OF CELL BIOLOGY
- Intrabody Gene Therapy Ameliorates Motor, Cognitive, and Neuropathological Symptoms in Multiple Mouse Models of Huntington's Disease
- (2009) A. L. Southwell et al. JOURNAL OF NEUROSCIENCE
- Polyglutamine disruption of the huntingtin exon 1 N terminus triggers a complex aggregation mechanism
- (2009) Ashwani K Thakur et al. NATURE STRUCTURAL & MOLECULAR BIOLOGY
- Secondary Structure of Huntingtin Amino-Terminal Region
- (2009) Mee Whi Kim et al. STRUCTURE
- SitePredicting the cleavage of proteinase substrates
- (2009) Jelle Verspurten et al. TRENDS IN BIOCHEMICAL SCIENCES
- Huntington's disease: from pathology and genetics to potential therapies
- (2008) Sara Imarisio et al. BIOCHEMICAL JOURNAL
- Autophagy: Principles and significance in health and disease
- (2008) Virginia Todde et al. BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE
- Mechanisms of neurodegeneration in Huntington’s disease
- (2008) Joana M. Gil et al. EUROPEAN JOURNAL OF NEUROSCIENCE
- Intrabodies Binding the Proline-Rich Domains of Mutant Huntingtin Increase Its Turnover and Reduce Neurotoxicity
- (2008) A. L. Southwell et al. JOURNAL OF NEUROSCIENCE
- Phosphorylation of huntingtin reduces the accumulation of its nuclear fragments
- (2008) Simon C. Warby et al. MOLECULAR AND CELLULAR NEUROSCIENCE
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