| Literature DB >> 17400507 |
Justus C Dächsel1, Julie P Taylor, Su San Mok, Owen A Ross, Kelly M Hinkle, Rachel M Bailey, Jacob H Hines, Jennifer Szutu, Benjamin Madden, Leonard Petrucelli, Matthew J Farrer.
Abstract
Pathogenic substitutions in the Lrrk2 protein have been shown to be an important cause of both familial and sporadic parkinsonism. The molecular pathway involved in Lrrk2 dopaminergic neuron degeneration remains elusive. Employing a combination of Lrrk2-mediated protein precipitation and tandem mass spectrometry, we identified 14 potential Lrrk2 binding partners. The majority of these interactions may be subgrouped into three functional cellular pathways: (i) chaperone-mediated response, (ii) proteins associated with the cytoskeleton and trafficking and (iii) phosphorylation and kinase activity. Future investigation of these candidates is now warranted and may help resolve the pathomechanism behind Lrrk2 neurodegeneration.Entities:
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Year: 2007 PMID: 17400507 PMCID: PMC2970619 DOI: 10.1016/j.parkreldis.2007.01.008
Source DB: PubMed Journal: Parkinsonism Relat Disord ISSN: 1353-8020 Impact factor: 4.891