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Exploring LRRK2 Substrate(s) for Parkinson Disease by Protein Arrays

Objective/Rationale: 
Mutations in the leucine-rich repeat kinase 2 (LRRK2) are the most common known cause of PD. A major gap in our understanding of how LRRK2 causes PD is the lack of knowledge of LRRK2 physiological substrate(s). Thus, we propose to identify LRRK2 substrate(s) using a newly developed Protein Microarray technology with human proteins.
Project Description: 
Increasing evidence suggests that LRRK2 is an upstream kinase in the signaling cascade that phosphorylates the downstream effectors (substrates). Thus, we will indentify LRRK2 substrate(s) by using a home-made high-throughput proteome chip with 4200 human proteins purified from a yeast expression system. We will then confirm the positive hits by various cell biology and biochemistry approaches. 
Relevance to Diagnosis/Treatment of Parkinson’s Disease: 
Identification of LRRK2 substrates will facilitate understanding of the molecular pathogenesis of LRRK2-related PD, provide potential innovative therapeutic targets, and help to develop the specific LRRK2 kinase assay and to screen for LRRK2 inhibitors to treat PD in future.
Anticipated Outcome: 
We anticipate that we will indentify LRRK2 substrate(s) from protein arrays and post confirmation experiments. If we identify a real substrate, it will lead to a series interesting projects for future studies: exploring the role of this substrate in PD pathogenesis and developing rational therape

Final Outcome

Dr. Smith identified five possible candidate hits for LRRK2 substrates using a protein array. One protein in particular, a kinase, was shown to interact with G2019S-LRRK2 and to be primarily expressed within the cytoplasm. Dr. Smith is working to further validate this candidate protein.


Researchers

  • Wanli W. Smith, PhD

    Baltimore, MD United States


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