Article

Sequential screening nominates the Parkinson’s disease associated kinase LRRK2 as a regulator of Clathrin-mediated endocytosis

2020-04-30

Abstract excerpt

Mutations in leucine-rich repeat kinase 2 ( LRRK2 ) are an established cause of inherited Parkinson’s disease (PD). LRRK2 is expressed in both neurons and glia in the central nervous system, but its physiological function(s) in each of these cell types is uncertain. Through sequential screens, we report a functional interaction between LRRK2 and Clathrin adaptor protein complex 2 (AP2). Analysis of LRRK2 KO tissu...

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Literature Corpus work: c77a5382-3e46-5e0f-b301-7f62649223cd
DOI: 10.1101/2020.04.28.053660

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