Overview
I am a tenured Professor with a primary appointment in Pharmacology and Cancer Biology, secondary appointments in Neurology and Neurobiology, and I serve as the director of the Duke Center for Neurodegeneration and Neurotherapeutics. Our main research efforts in the laboratory have focused on LRRK2 and alpha-synuclein in critical mechanisms and biomarkers in neurodegeneration and as possible therapeutic targets for disease modification strategies. I am a founding member of the NINDS Parkinson Disease Biomarker Program (PDBP) steering committee, a past member of the Executive Scientific Advisory Board at the Michael J. Fox Foundation (MJFF), current member of the NSD-B study section for the NINDS Office of Translational Research, and I am a board-reviewing editor for neurodegeneration research for eLife.
In training, i performed undergraduate research in the laboratory of Todd Golde focused on mechanisms of Ab toxicity, thesis work in the laboratories of John Hardy and Matthew Farrer (Mayo Clinic Parkinson’s Udall Center) focused on the genetics and genomics of parkin-linked PD, and post-doctoral work with Nigel Maidment (UCLA Udall Center) and Ted and Valina Dawson (Johns Hopkins Parkinson Udall Center) focused on LRRK2-linked Parkinson disease. I was previously an F31 and F32 individual NRSA recipient and was selected in the first wave of NIH’s K99 pipeline in 2006. Funding from both NINDS and MJFF has been continuous since the West laboratory opened in Birmingham in 2008 and continued with the move to Duke University in late 2018.
I have authored more than 100 publications characterizing biochemical mechanisms underlying neurodegeneration and neurodevelopmental disorders. The West laboratory serves as a hub for LRRK2 and a-synuclein research through freely sharing novel antibodies, recombinant proteins, DNA plasmids, viral constructs, animals, and protocols with dozens of laboratories and pharmaceutical
Current Appointments & Affiliations
In the News
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Recent Publications
Accumulation of LRRK2-associated phospho-Rab12 degenerative lysosomes in tauopathies
Preprint · June 9, 2025 Full text CiteLRRK2 interactions with microtubules are independent of LRRK2-mediated Rab phosphorylation.
Journal Article EMBO Rep · May 27, 2025 Deregulated microtubules are common defects associated with neurodegenerative diseases. Recent cryo-electron microscopy studies in cell lines overexpressing Parkinson's disease-associated LRRK2 suggest microtubule surfaces may regulate kinase activity by s ... Full text Link to item CiteDiscovery of a Chiral 2,4-Substituted Pyrrolo[2,3-d]pyrimidine as a Potent, Selective, and Orally Bioavailable LRRK2 Inhibitor.
Journal Article J Med Chem · May 22, 2025 Inhibition of leucine-rich repeat kinase (LRRK2) activity with small molecules has emerged as a potential novel therapeutic target for Parkinson's disease (PD). We have previously reported the identification of SRI-29132 as a potent LRRK2 inhibitor, but th ... Full text Link to item CiteRecent Grants
Neurobiology Training Program
Inst. Training Prgm or CMEMentor · Awarded by National Institutes of Health · 2024 - 2029Characterization of LRRK2 KO rats
ResearchPrincipal Investigator · Awarded by Michael J. Fox Foundation for Parkinson's Research · 2025 - 2026Role of enteroendocrine cells in the origin of Parkinson's pathology
ResearchCo Investigator · Awarded by Michael J. Fox Foundation for Parkinson's Research · 2021 - 2026View All Grants