ArticleMetabolomic Identification of the Target of the Filopodia Protrusion Inhibitor Glucopiericidin A
-
Add time:08/22/2019 Source:sciencedirect.com
SummaryIdentifying the targets of bioactive compounds is a major challenge in chemical biological research. Here, we identified the functional target of the natural bioactive compound glucopiericidin A (GPA) through metabolomic analysis. We isolated GPA while screening microbial samples for a filopodia protrusion inhibitor. Interestingly, GPA alone did not inhibit filopodia protrusion, but synergistically inhibit protrusion with the mitochondrial respiration inhibitor, piericidin A (PA). These results suggested that GPA might inhibit glycolysis. Capillary electrophoresis time-of-flight mass spectrometry (CE-TOFMS) provided strong evidence that GPA suppresses glycolysis by functionally targeting the glucose transporter. GPA may therefore serve as a glucose transporter chemical probe. Simultaneous inhibition of both glycolysis and mitochondrial respiration dramatically decreased intracellular ATP levels, indicating that GPA inhibits ATP-dependent filopodia protrusion with PA. Our results represent a challenge of molecular target identification using metabolomic analysis.
We also recommend Trading Suppliers and Manufacturers of glucopiericidin B (cas 108073-61-6). Pls Click Website Link as below: cas 108073-61-6 suppliers
Prev:Efficacies of quorum sensing inhibitors, piericidin A and glucopiericidin A, produced by Streptomyces xanthocidicus KPP01532 for the control of potato soft rot caused by Erwinia carotovora subsp. atroseptica
Next:Data ArticleStructural data of lanthanide complex constructed by 4-iodo-3-methyl benzoic acid and 4,7-dimethyl-1,10-phenanthroline) - 【Back】【Close 】【Print】【Add to favorite 】


