Erica Dhuey

ORCID: 0000-0002-5961-0722
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About
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Research Areas
  • Immune Cell Function and Interaction
  • Cancer Immunotherapy and Biomarkers
  • RNA and protein synthesis mechanisms
  • Bacteriophages and microbial interactions
  • CAR-T cell therapy research
  • Immune cells in cancer
  • HIV Research and Treatment
  • Immune responses and vaccinations

Stanford University
2024

University of Pennsylvania
2022

UPMC Hillman Cancer Center
2022

Cancer Research Institute
2022

New York University
2014

APOBEC3A (A3A), one of the seven-member APOBEC3 family cytidine deaminases, lacks strong antiviral activity against lentiviruses but is a potent inhibitor adeno-associated virus and endogenous retroelements. In this report, we characterize biochemical properties mammalian cell-produced catalytically active E. coli-produced A3A. The enzyme binds to single-stranded DNA with Kd 150 nM forms dimeric monomeric fractions. A3A, unlike APOBEC3G (A3G), deaminates substrates nonprocessively. Using...

10.1371/journal.pone.0097062 article EN cc-by PLoS ONE 2014-05-14

SUMMARY Availability of effective anti-tumor T cells is limited by cancer immunoediting, which depletes neoantigens, and central tolerance, eliminates developing with high-affinity cell receptors (TCRs) against tumor self-antigens. Remaining tumor-reactive are often exhausted after immune checkpoint blockade (ICB). Whether endogenous high- affinity TCRs self-antigens can be generated to circumvent exhaustion reject neoantigen-poor tumors unclear. We show that transiently interrupting...

10.1101/2022.01.19.476935 preprint EN cc-by-nc-nd bioRxiv (Cold Spring Harbor Laboratory) 2022-01-21
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