S K Joseph

Summary

Affiliation: Thomas Jefferson University
Country: USA

Publications

  1. ncbi Biosynthesis of inositol trisphosphate receptors: selective association with the molecular chaperone calnexin
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, PA 19107, USA
    Biochem J 342:153-61. 1999
  2. ncbi The inositol triphosphate receptor family
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, PA 19107, USA
    Cell Signal 8:1-7. 1996
  3. ncbi The interaction of calmodulin with alternatively spliced isoforms of the type-I inositol trisphosphate receptor
    C Lin
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 275:2305-11. 2000
  4. ncbi Factors determining the composition of inositol trisphosphate receptor hetero-oligomers expressed in COS cells
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 275:16084-90. 2000
  5. ncbi Molecular determinants of ion permeation and selectivity in inositol 1,4,5-trisphosphate receptor Ca2+ channels
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19103, USA
    J Biol Chem 276:13509-12. 2001
  6. ncbi Functional properties of recombinant type I and type III inositol 1, 4,5-trisphosphate receptor isoforms expressed in COS-7 cells
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 275:21492-9. 2000
  7. ncbi Direct association of ligand-binding and pore domains in homo- and heterotetrameric inositol 1,4,5-trisphosphate receptors
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, PA 19107, USA
    EMBO J 19:5450-9. 2000
  8. ncbi Angiotensin II-induced down-regulation of inositol trisphosphate receptors in WB rat liver epithelial cells. Evidence for involvement of the proteasome pathway
    S Bokkala
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 272:12454-61. 1997
  9. ncbi Membrane insertion, glycosylation, and oligomerization of inositol trisphosphate receptors in a cell-free translation system
    S K Joseph
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 272:1579-88. 1997
  10. ncbi Single-channel recordings of recombinant inositol trisphosphate receptors in mammalian nuclear envelope
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19103, USA
    Biophys J 81:117-24. 2001

Collaborators

Detail Information

Publications18

  1. ncbi Biosynthesis of inositol trisphosphate receptors: selective association with the molecular chaperone calnexin
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, PA 19107, USA
    Biochem J 342:153-61. 1999
    ..We propose that calnexin is a key chaperone involved in the folding, assembly and oligomerization of newly synthesized IP(3) receptors in the ER...
  2. ncbi The inositol triphosphate receptor family
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, PA 19107, USA
    Cell Signal 8:1-7. 1996
    ..Most cell types appear to contain multiple receptor isoforms. The review summarizes recent progress on IP3 receptor biology with a particular emphasis on distinctive structural and regulatory features of the individual isoforms...
  3. ncbi The interaction of calmodulin with alternatively spliced isoforms of the type-I inositol trisphosphate receptor
    C Lin
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 275:2305-11. 2000
    ..We conclude that the deletion of the SII splice site in the type-I IP(3)R results in the differential regulation of the alternatively spliced isoforms by Ca(2+), CaM, and protein kinase A...
  4. ncbi Factors determining the composition of inositol trisphosphate receptor hetero-oligomers expressed in COS cells
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 275:16084-90. 2000
    ..However, hetero-oligomers were synthesized with a longer lag period, suggesting that there may be kinetic constraints that favor homo-oligomers over hetero-oligomers...
  5. ncbi Molecular determinants of ion permeation and selectivity in inositol 1,4,5-trisphosphate receptor Ca2+ channels
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19103, USA
    J Biol Chem 276:13509-12. 2001
    ..We propose that the pore of IP(3)R channels has two distinct sites that control monovalent cation permeation (Val(2548)) and Ca(2+) selectivity (Asp(2550))...
  6. ncbi Functional properties of recombinant type I and type III inositol 1, 4,5-trisphosphate receptor isoforms expressed in COS-7 cells
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 275:21492-9. 2000
    ..This assay therefore provides a useful tool for studying the regulatory properties of individual IP(3)R isoforms as well as for screening pore mutations prior to more detailed electrophysiological analyses...
  7. ncbi Direct association of ligand-binding and pore domains in homo- and heterotetrameric inositol 1,4,5-trisphosphate receptors
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, PA 19107, USA
    EMBO J 19:5450-9. 2000
    ....
  8. ncbi Angiotensin II-induced down-regulation of inositol trisphosphate receptors in WB rat liver epithelial cells. Evidence for involvement of the proteasome pathway
    S Bokkala
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 272:12454-61. 1997
    ..We conclude that Ang II-stimulated IP3R degradation involves enhanced ubiquitination of the protein and degradation by the proteasome pathway...
  9. ncbi Membrane insertion, glycosylation, and oligomerization of inositol trisphosphate receptors in a cell-free translation system
    S K Joseph
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 272:1579-88. 1997
    ..A second oligomerization domain involved in stabilization of heteroligomers is present within the first four transmembrane domains...
  10. ncbi Single-channel recordings of recombinant inositol trisphosphate receptors in mammalian nuclear envelope
    D Boehning
    Department of Pathology and Cell Biology, Thomas Jefferson University, Philadelphia, Pennsylvania 19103, USA
    Biophys J 81:117-24. 2001
    ..This approach provides a powerful new methodology to study the permeation and gating properties of recombinant mammalian InsP(3)Rs in a native mammalian membrane environment at the single-channel level...
  11. ncbi Transforming growth factor-beta1 inhibits type I inositol 1,4,5-trisphosphate receptor expression and enhances its phosphorylation in mesangial cells
    K Sharma
    Department of Medicine, Nephrology Division, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 272:14617-23. 1997
    ..It is proposed that TGF-beta-mediated effects on the IP3R may be an important characteristic of its ability to modulate the response of cells to factors that employ IP3R-mediated calcium release...
  12. ncbi Effect of mutation of a calmodulin binding site on Ca2+ regulation of inositol trisphosphate receptors
    X Zhang
    Department of Pathology, Thomas Jefferson University, Philadelphia, PA 19107, USA
    Biochem J 360:395-400. 2001
    ....
  13. ncbi Renal type I inositol 1,4,5-trisphosphate receptor is reduced in streptozotocin-induced diabetic rats and mice
    K Sharma
    Nephrology Division, Pathology, and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    Am J Physiol 276:F54-61. 1999
    ..These findings demonstrate that there is reduced type I IP3R in glomerular and vascular smooth muscle cells in the diabetic kidney, which may contribute to the altered renal vasoregulation and renal hypertrophy of diabetes...
  14. ncbi Characterization of membrane-associated proteasomes in WB rat liver epithelial cells
    M T Khan
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    Arch Biochem Biophys 385:99-107. 2001
    ..Thus, the principal difference between cytosolic and membrane activity was that the latter fractions contained a novel membrane-associated LC-insensitive protease(s) catalyzing three of the major peptidase activities of the proteasome...
  15. ncbi The effect of mersalyl on inositol trisphosphate receptor binding and ion channel function
    S K Joseph
    Department of Pathology and Cell Biology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107
    J Biol Chem 270:3588-93. 1995
    ..This contrasts with the high affinity receptor/active Ca2+ channel induced by thimerosal, suggesting that even closely related thiol agents may interact at different thiol groups...
  16. ncbi Single-channel properties in endoplasmic reticulum membrane of recombinant type 3 inositol trisphosphate receptor
    D O Mak
    Department of Physiology, University of Pennsylvania, Philadelphia, Pennsylvania 19104, USA
    J Gen Physiol 115:241-56. 2000
    ....
  17. ncbi Heteroligomers of type-I and type-III inositol trisphosphate receptors in WB rat liver epithelial cells
    S K Joseph
    Department of Pathology, Thomas Jefferson University School of Medicine, Philadelphia, Pennsylvania 19107, USA
    J Biol Chem 270:23310-6. 1995
    ..We conclude that the WB cell contains both type-I and type-III IP3R isoforms and that a proportion of these receptors exist as heterotetramers...
  18. ncbi Effect of angiotensin II and ethanol on the expression of connexin 43 in WB rat liver epithelial cells
    S Bokkala
    Department of Pathology, Anatomy and Cell Biology, Thomas Jefferson University, 1020 Locust Street, Philadelphia, PA 19107, USA
    Biochem J 357:769-77. 2001
    ..We conclude that Cx43 biosynthesis is regulated by Ca(2+)-mobilizing agonists and ethanol in WB cells. The changes in Cx43 expression might have a role in modifying the conduction of metabolites and second messengers between cells...