作者: Samantha J Orenstein , Sheng-Han Kuo , Inmaculada Tasset , Esperanza Arias , Hiroshi Koga
DOI: 10.1038/NN.3350
关键词: Mutant 、 Autophagy 、 LRRK2 、 Transgene 、 Genetically modified mouse 、 Kinase 、 Chaperone-mediated autophagy 、 HEK 293 cells 、 Biology 、 Molecular biology
摘要: Mutations in leucine-rich repeat kinase 2 (LRRK2) are the most common cause of familial Parkinson's disease. We found LRRK2 to be degraded in lysosomes by chaperone-mediated …