Autophosphorylation of serine 608 in the p85 regulatory subunit of wild type or cancer-associated mutants of phosphoinositide 3-kinase does not affect its lipid kinase activity |
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Authors: | Meredith J Layton Mirette Saad Nicole L Church Richard B Pearson Christina A Mitchell Wayne A Phillips |
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Institution: | 1. Department of Biochemistry and Molecular Biology, The University of Oklahoma Health Sciences Center, (940 S. L. Young Blvd), Oklahoma City, OK, 73104, USA 2. The Peggy and Charles Stephenson Oklahoma Cancer Center, The University of Oklahoma Health Sciences Center, (940 S. L. Young Blvd), Oklahoma City, OK, 73104, USA 3. The Oklahoma Center for Medical Glycobiology, The University of Oklahoma Health Sciences Center, (940 S. L. Young Blvd), Oklahoma City, OK, 73104, USA
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Abstract: | Background Hyaluronan (HA) is made at the plasma membrane and secreted into the extracellular medium or matrix by phospolipid-dependent hyaluronan synthase (HAS), which is active as a monomer. Since the mechanism by which HA is translocated across membranes is still unresolved, we assessed the presence of an intraprotein pore within HAS by adding purified Streptococcus equisimilis HAS (SeHAS) to liposomes preloaded with the fluorophore Cascade Blue (CB). Results CB translocation (efflux) was not observed with mock-purified material from empty vector control E. coli membranes, but was induced by SeHAS, purified from membranes, in a time- and dose-dependent manner. CB efflux was eliminated or greatly reduced when purified SeHAS was first treated under conditions that inhibit enzyme activity: heating, oxidization or cysteine modification with N-ethylmaleimide. Reduced CB efflux also occurred with SeHAS K48E or K48F mutants, in which alteration of K48 within membrane domain 2 causes decreased activity and HA product size. The above results used liposomes containing bovine cardiolipin (BCL). An earlier study testing many synthetic lipids found that the best activating lipid for SeHAS is tetraoleoyl cardiolipin (TO-CL) and that, in contrast, tetramyristoyl cardiolipin (TM-CL) is an inactivating lipid (Weigel et al, J. Biol. Chem. 281, 36542, 2006). Consistent with the effects of these CL species on SeHAS activity, CB efflux was more than 2-fold greater in liposomes made with TO-CL compared to TM-CL. Conclusions The results indicate the presence of an intraprotein pore in HAS and support a model in which HA is translocated to the exterior by HAS itself. |
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