David Eliezer
· Professor of Biochemistry and BiophysicsCornell University · Biochemistry and Molecular Biology
Active 1989–2025
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About
David Eliezer, Ph.D., is a Professor of Biochemistry and Biophysics at Weill Cornell Medicine. His research primarily involves the application of NMR spectroscopy to problems in non-native structural biology, with a focus on characterizing the location, extent of structure, and intermolecular interactions of aggregation-competent partially unfolded states of proteins involved in neurodegenerative diseases. His specific targets include proteins related to Alzheimer's Disease and Parkinson's Disease. The Eliezer laboratory aims to better understand α-synuclein, a neuronal protein associated with Parkinson’s disease, in both healthy and diseased brains by studying its membrane-bound and aggregated states. His work contributes to the understanding of protein misfolding and aggregation processes relevant to neurodegenerative conditions.
Research topics
- Internal medicine
- Anatomy
- Medicine
- Neuroscience
- Biology
Selected publications
Nature Neuroscience · 2020 · 124 citations
Science Advances · 2024-08-21 · 29 citations
articleOpen accessAlthough certain drivers of familial Parkinson's disease (PD) compromise mitochondrial integrity, whether metabolic deficits underly other idiopathic or genetic origins of PD is unclear. Here, we demonstrate that phosphoglycerate kinase 1 (PGK1), a gene in the PARK12 susceptibility locus, is rate limiting in neuronal glycolysis and that modestly increasing PGK1 expression boosts neuronal adenosine 5'-triphosphate production kinetics that is sufficient to suppress PARK20-driven synaptic dysfuncti…
npj Parkinson s Disease · 2023-09-23 · 26 citations
articleOpen accessCorrespondingAbstract Alpha synuclein (a-syn) is an intrinsically disordered protein prevalent in neurons, and aggregated forms are associated with synucleinopathies including Parkinson’s disease (PD). Despite the biomedical importance and extensive studies, the physiological role of a-syn and its participation in etiology of PD remain uncertain. We showed previously in model RBL cells that a-syn colocalizes with mitochondrial membranes, depending on formation of N-terminal helices and increasing with mitoch…
Acta Biomaterialia · 2024-06-05 · 23 citations
articleOpen accessProceedings of the National Academy of Sciences · 2024-07-10 · 11 citations
articleOpen accessSenior authorCorrespondingG protein-coupled receptors (GPCRs) control intracellular signaling cascades via agonist-dependent coupling to intracellular transducers including heterotrimeric G proteins, GPCR kinases (GRKs), and arrestins. In addition to their critical interactions with the transmembrane core of active GPCRs, all three classes of transducers have also been reported to interact with receptor C-terminal domains (CTDs). An underexplored aspect of GPCR CTDs is their possible role as lipid sensors given their pro…
Recent grants
NIH · $75k
NIH · $2.6M · 2010
NIH · $1.2M · 2010
Frequent coauthors
- 40 shared
Vladimir N. Uversky
- 40 shared
Sebastian Doniach
Stanford University
- 39 shared
Keith O. Hodgson
Stanford Synchrotron Radiation Lightsource
- 36 shared
Anthony L. Fink
- 36 shared
Daniel J. Segel
Stanford University
- 35 shared
Tapojyoti Das
St. Jude Children's Research Hospital
- 34 shared
Trudy F. Ramlall
Regeneron (United States)
- 32 shared
Diana Acosta
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