
Cornelius Y Taabazuing
VerifiedUniversity of Pennsylvania · Rehabilitation Medicine
Active 2011–2024
Research topics
- Biology
- Sociology
- Social Science
- Gender studies
- Genetics
- Environmental ethics
- Cell biology
- Engineering ethics
Selected publications
Juneteenth in STEMM and the barriers to equitable science
Cell · 2023 · 28 citations
- Sociology
- Social Science
- Biology
The NLRP1 and CARD8 inflammasomes
Immunological Reviews · 2020 · 179 citations
1st authorCorresponding- Biology
- Cell biology
- Genetics
Inflammasomes are multiprotein complexes that activate inflammatory cytokines and induce pyroptosis in response to intracellular danger-associated signals. NLRP1 and CARD8 are related germline-encoded pattern recognition receptors that form inflammasomes, but their activation mechanisms and biological purposes have not yet been fully established. Both NLRP1 and CARD8 undergo post-translational autoproteolysis to generate two non-covalently associated polypeptide chains. NLRP1 and CARD8 activators induce the proteasome-mediated destruction of the N-terminal fragment, liberating the C-terminal fragment to form an inflammasome. Here, we review the danger-associated stimuli that have been reported to activate NLRP1 and/or CARD8, including anthrax lethal toxin, Toxoplasma gondii, Shigella flexneri and the small molecule DPP8/9 inhibitor Val-boroPro, focusing on recent mechanistic insights and highlighting unresolved questions. In addition, we discuss the recently identified disease-associated mutations in NLRP1 and CARD8, the potential role that DPP9's protein structure plays in inflammasome regulation, and the emerging link between NLRP1 and metabolism. Finally, we summarize all of this latest research and consider the possible biological purposes of these enigmatic inflammasomes.
Frequent coauthors
- 29 shared
Daniel A. Bachovchin
Tri-Institutional PhD Program in Chemical Biology
- 21 shared
Andrew R. Griswold
Tri-Institutional PhD Program in Chemical Biology
- 16 shared
Ashley J. Chui
Tri-Institutional PhD Program in Chemical Biology
- 14 shared
Elizabeth L. Orth-He
Tri-Institutional PhD Program in Chemical Biology
- 14 shared
Sahana D. Rao
Tri-Institutional PhD Program in Chemical Biology
- 11 shared
Michael J. Knapp
University of Massachusetts Amherst
- 10 shared
Darren C. Johnson
Pfizer (United States)
- 7 shared
John A. Hangasky
ProLynx (United States)
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