# Changes in synaptic vesicle-binding of alpha-synuclein in the central and enteric nervous system > **NIH NIH R01** · WEILL MEDICAL COLL OF CORNELL UNIV · 2022 · $64,410 ## Abstract PROJECT SUMMARY/ABSTRACT Alpha-synuclein (αSyn) pathology is linked to synucleinopathies including Parkinson's disease and Lewy body dementia, but the underlying disease mechanisms remain poorly understood. The prevalent viewpoint has emerged that aggregation of αSyn triggers neuropathology through a gain-of-toxic-function mechanism, and approaches to eliminate αSyn represent an active area of research for treatment. Yet, αSyn aggregation may also endanger neurons by removing αSyn from synaptic vesicles (its physiologically relevant intracellular location) and thereby causing loss-of-function. Through its synaptic vesicle-bound state, αSyn regulates synaptic vesicle trafficking, and chaperones SNARE-complex assembly to maintain neurotransmitter release. Thus, removing αSyn from neurons may not be protective, but detrimental. The objective in this application is to determine the impact of synaptic vesicle-binding of αSyn on αSyn function and neuron survival, using rationally designed variants of αSyn that stabilize synaptic vesicle-binding. The central hypothesis is that stabilizing binding of αSyn on synaptic vesicles reduces αSyn toxicity and pathology. Guided by strong preliminary data, this hypothesis will be tested in three specific aims: 1) Determine the effect of increased synaptic vesicle-binding of αSyn on SNARE-complex assembly; 2) Assess the effect of increased synaptic vesicle-binding of αSyn on synaptic vesicle cycling; and 3) Test if increased synaptic vesicle-binding of αSyn rescues neurotoxicity and pathology in vivo. Under the first aim, SNARE-complex assembly will be quantified in vivo and in vitro, using cell biological and biochemical techniques. Under the second aim, αSyn multimerization, synaptic vesicle pools and clustering, and synaptic vesicle cycling will be quantified, using cell biological, biochemical and biophysical techniques. Under the third aim, mouse models will be generated by stereotactic injections of lentiviral vectors into the substantia nigra of αSyn knockout mice to assess effects of mutant αSyn variants on αSyn-induced toxicity and pathology, using behavioral assays on mice and biochemical, histological and ultrastructural analyses on injected brains. The study is expected to show improved αSyn function and delayed pathology upon stabilization of synaptic vesicle-binding of αSyn. This research is innovative because it 1) tests the novel hypothesis that stabilizing synaptic vesicle-bound αSyn reduces αSyn pathology, 2) creates new tools to study function and dysfunction of αSyn, and 3) uses a multidisciplinary approach to test our hypothesis from single molecules and cellular systems to live mice. This work is significant, because it will 1) clarify the importance of synaptic vesicle-binding of αSyn for neuron function, 2) provide new insights into the molecular mechanism of synaptic vesicle-binding of αSyn, 3) uncover the contribution of loss-of-function of αSyn to disease pathogenesis, and 4) have transla... ## Key facts - **NIH application ID:** 10527040 - **Project number:** 3R01NS113960-02S1 - **Recipient organization:** WEILL MEDICAL COLL OF CORNELL UNIV - **Principal Investigator:** Jacqueline Burre - **Activity code:** R01 (R01, R21, SBIR, etc.) - **Funding institute:** NIH - **Fiscal year:** 2022 - **Award amount:** $64,410 - **Award type:** 3 - **Project period:** 2022-06-01 → 2023-05-31 ## Primary source NIH RePORTER: https://reporter.nih.gov/project-details/10527040 ## Citation > US National Institutes of Health, RePORTER application 10527040, Changes in synaptic vesicle-binding of alpha-synuclein in the central and enteric nervous system (3R01NS113960-02S1). Retrieved via AI Analytics 2026-05-25 from https://api.ai-analytics.org/grant/nih/10527040. Licensed CC0. --- *[NIH grants dataset](/datasets/nih-grants) · CC0 1.0*