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• W2893756021 abstract "15-deoxy-delta 12,14-prostaglandin J2 (15d-PGJ2) is anti-inflammatory/anti-neoplastic prostaglandin which functions through covalent binding to cysteine residues of various target proteins. We previously showed that 15d-PGJ2 mediated anti-inflammatory responses are dependent on the translational inhibition through its interaction with eIF4A. Binding of 15d-PGJ2 to eIF4A specifically blocks the interaction between eIF4G and eIF4A leads to the formation of stress granules (SGs), which cluster mRNAs with inhibited translation. Here we show that the binding between 15d-PGJ2 and eIF4A specifically blocks the interaction between the MIF4G domain of eIF4G and eIF4A. To reveal the mechanism of this interaction, we used computational simulation-based docking studies and identified that the carboxyl tail of 15d-PGJ2 could stabilize the binding of 15d-PGJ2 to eIF4A through arginine 295 of eIF4A, which is the first suggestion that the 15d-PGJ2 tail play a physiological role. Interestingly, the putative 15d-PGJ2 binding site on eiF4A is conserved across many species, suggesting a biological role. Our data propose that studying 15d-PGJ2 and its targets will may uncover new therapeutic approaches in anti-inflammatory drug discovery." @default.
• W2893756021 created "2018-10-05" @default.
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• W2893756021 date "2018-01-01" @default.
• W2893756021 modified "2023-10-05" @default.
• W2893756021 title "The mechanistic insight of a specific interaction between 15d-Prostaglandin-J2 and eIF4A suggests an evolutionary conserved role across species" @default.
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• W2893756021 doi "https://doi.org/10.1242/bio.035402" @default.
• W2893756021 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/6262856" @default.
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