The Dengue virus protease NS2B3 cleaves cyclic GMP-AMP synthase to suppress cGAS activation.
Ontology highlight
ABSTRACT: Dengue virus (DENV) is one of the most prevalent mosquito-transmitted human viruses that causes significant morbidity and mortality worldwide. To persist in the cell and consequently cause disease, DENV is evolved with mechanisms to suppress the induction of type I interferons by antagonizing cGAS-STING signaling. Using recombinant proteins and in vitro cleavage assays, we have shown that the DENV protease NS2B3 is capable of cleaving cGAS in the N-terminal region without disrupting the C-terminal catalytic center. This generates two major cleavage products: cleavage product N-terminal (CP-N) and cleavage product C-terminal (CP-C). We observed reduction in DNA-binding affinity of CP-C as compared to full-length cGAS. Reduction in DNA-binding affinity is also correlated with the decrease in
SUBMITTER: Bhattacharya M
PROVIDER: S-EPMC10011430 | biostudies-literature | 2023 Feb
REPOSITORIES: biostudies-literature
ACCESS DATA