4 research outputs found
PKCĪ± Regulates Phosphorylation and Enzymatic Activity of cPLA2 In Vitro and in Activated Human Monocytes
Phospholipases A (PLA ) are potent regulators of the inflammatory response. We have observed that Group IV cPLA activity is required for the production of superoxide anion (O ) in human monocytes [Li Q., Cathcart M.K. J. Biol. Chem. 272 (4) (1997) 2404-2411.]. We have previously identified PKCĪ± as a kinase pathway required for monocyte O production [Li Q., Cathcart M.K. J. Biol. Chem. 269 (26) (1994) 17508-17515.]. We therefore investigated the potential interaction between PKCĪ± and cPLA by evaluating the requirement for specific PKC isoenzymes in the process of activating cPLA enzymatic activity and protein phosphorylation upon monocyte activation. We first showed that general PKC inhibitors and antisense oligodeoxyribonucleotides (ODN) to the cPKC group of PKC enzymes inhibited cPLA activity. To distinguish between PKCĪ± and PKCĪ² isoenzymes in regulating cPLA protein phosphorylation and enzymatic activity, we employed our previously characterized PKCĪ± or PKCĪ² isoenzyme-specific antisense ODN [Li Q., Subbulakshmi V., Fields A.P., Murray, N.R., Cathcart M.K., J. Biol. Chem. 274 (6) (1999) 3764-3771]. Suppression of PKCĪ± expression, but not PKCĪ² expression, inhibited cPLA protein phosphorylation and enzymatic activity. Additional studies ruled out a contribution by Erk1/2 to cPLA phosphorylation and activation. We also found that cPLA co-immunoprecipitated with PKCĪ± and vice versa. In vitro studies demonstrated that PKCĪ± could directly phosphorylate cPLA .and enhance enzymatic activity. Finally, we showed that addition of arachidonic acid restored the production of O in monocytes defective in either PKCĪ± or cPLA expression. Taken together, our data suggest that PKCĪ±, but not PKCĪ², is the predominant cPKC isoenzyme required for cPLA protein phosphorylation and maximal induction of cPLA enzymatic activity upon activation of human monocytes. Our data also support the concept that the requirements for PKCĪ± and cPLA in O generation are solely due to their seminal role in generating arachidonic acid. Ā© 2006 Elsevier Inc. All rights reserved. 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 2 - - -
Discovery of benzothiazoles as antimycobacterial agents: Synthesis, structure-activity relationships and binding studies with Mycobacterium tuberculosis decaprenylphosphoryl-beta-D-ribose 2 '-oxidase
We report the discovery of benzothiazoles, a novel anti-mycobacterial series, identified from a whole cell based screening campaign. Benzothiazoles exert their bactericidal activity against Mycobacterium tuberculosis (Mtb) through potent inhibition of decaprenylphosphoryl-beta-D-ribose 2'-oxidase (DprE1), the key enzyme involved in arabinogalactan synthesis. Specific target linkage and mode of binding were established using co-crystallization and protein mass spectrometry studies. Most importantly, the current study provides insights on the utilization of systematic medicinal chemistry approaches to mitigate safety liabilities while improving potency during progression from an initial genotoxic hit, the benzothiazole N-oxides (BTOs) to the lead-like AMES negative, crowded benzothiazoles (cBTs). These findings offer opportunities for development of safe clinical candidates against tuberculosis. The design strategy adopted could find potential application in discovery of safe drugs in other therapy areas too. (c) 2015 Elsevier Ltd. All rights reserved