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Your search keyword '"Shears, Stephen B."' showing total 17 results
Start Over Author "Shears, Stephen B." Publisher portland press ltd.
17 results on '"Shears, Stephen B."'

8. Intracellular localization of human Ins(1,3,4,5,6)P5 2-kinase

Author

Brehm, Maria A., primary, Schenk, Tobias M. H., additional, Zhou, Xuefei, additional, Fanick, Werner, additional, Lin, Hongying, additional, Windhorst, Sabine, additional, Nalaskowski, Marcus M., additional, Kobras, Mario, additional, Shears, Stephen B., additional, and Mayr, Georg W., additional

Published
2007
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13. PPIP5K1 modulates ligand competition between diphosphoinositol polyphosphates and PtdIns(3,4,5)P3 for polyphosphoinositide-binding domains.

Author

GOKHALE, Nikhil A., ZAREMBA, Angelika, JANOSHAZI, Agnes K., WEAVER, Jeremy D., and SHEARS, Stephen B.

Subjects
KINASES, PHOSPHORYLATION, CELLS, PLATELET-derived growth factor, CYTOPLASM, CELL membranes, MUTAGENESIS, PLASMONS (Physics)
Abstract

We describe new signalling consequences for PPIP5K1 (diphosphoinositol pentakisphosphate kinase type 1)-mediated phosphorylation of InsP6 and 5-InsP7 to 1-InsP7 and InsP8. In NIH 3T3 cells, either hyperosmotic stress or receptor activation by PDGF (platelet-derived growth factor) promoted translocation of PPIP5K1 from the cytoplasm to the plasma membrane. The PBD1 (polyphosphoinositide-binding domain) in PPIP5K1 recapitulated that translocation. Mutagenesis of PBD1 to reduce affinity for PtdIns(3,4,5)P3 prevented translocation. Using surface plasmon resonance, we found that PBD1 association with vesicular PtdIns(3,4,5)P3 was inhibited by InsP6 and diphosphoinositol polyphosphates. However, the inhibition by PPIP5K1 substrates (IC50: 5-InsP7 =5 μM and InsP6 =7 μM) was substantially more potent than that of the PPIP5K1 products (IC50: InsP8 =32 ìM and 1-InsP7 =43 μM). This rank order of ligand competition with PtdIns(3,4,5)P3 was also exhibited by the PH (pleckstrin homology) domains of Akt (also known as protein kinase B), GRP1 (general receptor for phosphoinositides 1) and SIN1 (stress-activated protein kinase-interaction protein 1). We propose that, in vivo, PH domain binding of InsP6 and 5-InsP7 suppresses inappropriate signalling ('noise') from stochastic increases in PtdIns(3,4,5)P3. That restraint may be relieved by localized depletion of InsP6 and 5-InsP7 at the plasma membrane following PPIP5K1 recruitment. We tested this hypothesis in insulin-stimulated L6 myoblasts, using mTOR (mechanistic/mammalian target of rapamycin)-mediated phosphorylation of Akt on Ser473 as a readout for SIN1-mediated translocation of mTORC (mTOR complex) 2 to the plasma membrane [Zoncu, Efeyan and Sabatini (2011) Nat. Rev. Mol. Cell Biol. 12, 21-35]. Knockdown of PPIP5K1 expression was associated with a 40% reduction in Ser473 phosphorylation. A common feature of PtdIns(3,4,5)P3-based signalling cascades may be their regulation by PPIP5K1. [ABSTRACT FROM AUTHOR]

Published
2013
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14. Localization of a high-affinity inositol 1,4,5-trisphosphate/inositol 1,4,5,6-tetrakisphosphate binding domain to the pleckstrin homology module of a new 130 kDa protein: characterization of the determinants of structural specificity

Author

TAKEUCHI, Hiroshi, primary, KANEMATSU, Takashi, additional, MISUMI, Yoshio, additional, YAAKOB, Hassan Bin, additional, YAGISAWA, Hitoshi, additional, IKEHARA, Yukio, additional, WATANABE, Yutaka, additional, TAN, Zheng, additional, SHEARS, Stephen B., additional, and HIRATA, Masato, additional

Published
1996
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