| Literature DB >> 28406616 |
Tobias Vöpel1, Kenny Bravo-Rodriguez2, Sumit Mittal2, Shivang Vachharajani1, David Gnutt1, Abhishek Sharma1, Anne Steinhof3, Oluwaseun Fatoba4, Gisa Ellrichmann4, Michael Nshanian5, Christian Heid6, Joseph A Loo5,7, Frank-Gerrit Klärner6, Thomas Schrader6, Gal Bitan8, Erich E Wanker3, Simon Ebbinghaus1, Elsa Sanchez-Garcia2.
Abstract
Huntington's disease is a neurodegenerative disorder associated with the expansion of the polyglutamine tract in the exon-1 domain of the huntingtin protein (htte1). Above a threshold of 37 glutamine residues, htte1 starts to aggregate in a nucleation-dependent manner. A 17-residue N-terminal fragment of htte1 (N17) has been suggested to play a crucial role in modulating the aggregation propensity and toxicity of htte1. Here we identify N17 as a potential target for novel therapeutic intervention using the molecular tweezer CLR01. A combination of biochemical experiments and computer simulations shows that binding of CLR01 induces structural rearrangements within the htte1 monomer and inhibits htte1 aggregation, underpinning the key role of N17 in modulating htte1 toxicity.Entities:
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Year: 2017 PMID: 28406616 PMCID: PMC5506490 DOI: 10.1021/jacs.6b11039
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419