JASON HAUGH

Summary

Affiliation: North Carolina State University
Country: USA

Publications

  1. ncbi A unified model for signal transduction reactions in cellular membranes
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695 7905 USA
    Biophys J 82:591-604. 2002
  2. ncbi Analysis of reaction-diffusion systems with anomalous subdiffusion
    Jason M Haugh
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA
    Biophys J 97:435-42. 2009
  3. ncbi Deterministic model of dermal wound invasion incorporating receptor-mediated signal transduction and spatial gradient sensing
    Jason M Haugh
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 90:2297-308. 2006
  4. ncbi Mathematical model of human growth hormone (hGH)-stimulated cell proliferation explains the efficacy of hGH variants as receptor agonists or antagonists
    Jason M Haugh
    Department of Chemical Engineering North Carolina State University, Raleigh, North Carolina 27695 7905, USA
    Biotechnol Prog 20:1337-44. 2004
  5. ncbi Localization of receptor-mediated signal transduction pathways: the inside story
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, NC 27695 7905, USA
    Mol Interv 2:292-307. 2002
  6. ncbi Spatial analysis of 3' phosphoinositide signaling in living fibroblasts: I. Uniform stimulation model and bounds on dimensionless groups
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 86:589-98. 2004
  7. ncbi Active EGF receptors have limited access to PtdIns(4,5)P(2) in endosomes: implications for phospholipase C and PI 3-kinase signaling
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, NC 27695 7905, USA
    J Cell Sci 115:303-10. 2002
  8. ncbi Spatial analysis of 3' phosphoinositide signaling in living fibroblasts: II. Parameter estimates for individual cells from experiments
    Ian C Schneider
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 86:599-608. 2004
  9. ncbi Structure-based kinetic models of modular signaling protein function: focus on Shp2
    Dipak Barua
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 92:2290-300. 2007
  10. ncbi Reactions on cell membranes: comparison of continuum theory and Brownian dynamics simulations
    Michael I Monine
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Box 7905, 911 Partners Way, Raleigh, North Carolina 27695-7905, USA
    J Chem Phys 123:074908. 2005

Collaborators

  • Ian C Schneider
  • Dipak Barua
  • Michael C Weiger
  • Michael I Monine
  • Murat Cirit
  • Chun Chao Wang
  • James R Faeder
  • Chang Shin Park
  • Erik S Welf
  • Matej Krajcovic
  • Harjeet Kaur
  • Shoeb Ahmed
  • Alan F Horwitz
  • Colin K Choi
  • John J Rhoden
  • Adam T Melvin
  • Jodee M Lewis
  • Elizabeth M Parrish

Detail Information

Publications25

  1. ncbi A unified model for signal transduction reactions in cellular membranes
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695 7905 USA
    Biophys J 82:591-604. 2002
    ..Under these conditions, however, enhanced substrate delivery can result in a decrease in the average substrate concentration...
  2. ncbi Analysis of reaction-diffusion systems with anomalous subdiffusion
    Jason M Haugh
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA
    Biophys J 97:435-42. 2009
    ..In each case, there are only subtle differences between the two subdiffusion models, suggesting how measurements of mean-squared displacement versus time might generally inform models of reactive systems with partial diffusion control...
  3. ncbi Deterministic model of dermal wound invasion incorporating receptor-mediated signal transduction and spatial gradient sensing
    Jason M Haugh
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 90:2297-308. 2006
    ..A somewhat surprising finding was that extremely sharp PDGF gradients do not necessarily stimulate faster progression through the clot, because maintaining such a gradient through PDGF consumption is a potentially rate-limiting process...
  4. ncbi Mathematical model of human growth hormone (hGH)-stimulated cell proliferation explains the efficacy of hGH variants as receptor agonists or antagonists
    Jason M Haugh
    Department of Chemical Engineering North Carolina State University, Raleigh, North Carolina 27695 7905, USA
    Biotechnol Prog 20:1337-44. 2004
    ....
  5. ncbi Localization of receptor-mediated signal transduction pathways: the inside story
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, NC 27695 7905, USA
    Mol Interv 2:292-307. 2002
    ..Still, only when the effects of decreased receptor populations and signaling compartmentalization are integrated can we hope to understand and manipulate receptor function at the molecular level...
  6. ncbi Spatial analysis of 3' phosphoinositide signaling in living fibroblasts: I. Uniform stimulation model and bounds on dimensionless groups
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 86:589-98. 2004
    ..Based on our analysis, we expect that the key dimensionless group, the ratio of 3' PI turnover and diffusion rates, can be estimated within approximately 20% or less...
  7. ncbi Active EGF receptors have limited access to PtdIns(4,5)P(2) in endosomes: implications for phospholipase C and PI 3-kinase signaling
    Jason M Haugh
    Department of Chemical Engineering, North Carolina State University, Raleigh, NC 27695 7905, USA
    J Cell Sci 115:303-10. 2002
    ....
  8. ncbi Spatial analysis of 3' phosphoinositide signaling in living fibroblasts: II. Parameter estimates for individual cells from experiments
    Ian C Schneider
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 86:599-608. 2004
    ..18 +/- 0.54 min(-1). In addition, we report that 3' PI turnover is not affected by PDGF receptor signaling in our cells, allowing us to focus our attention on the regulation of 3' PI production as this system is studied further...
  9. ncbi Structure-based kinetic models of modular signaling protein function: focus on Shp2
    Dipak Barua
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 92:2290-300. 2007
    ....
  10. ncbi Reactions on cell membranes: comparison of continuum theory and Brownian dynamics simulations
    Michael I Monine
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Box 7905, 911 Partners Way, Raleigh, North Carolina 27695-7905, USA
    J Chem Phys 123:074908. 2005
    ..In all cases, we find the theory and simulations to be in quantitative agreement. This algorithm may be readily adapted for the stochastic simulation of more complex cell signaling systems...
  11. ncbi Kinetic analysis of platelet-derived growth factor receptor/phosphoinositide 3-kinase/Akt signaling in fibroblasts
    Chang Shin Park
    Department of Chemical Engineering, North Carolina State University, Raleigh, North Carolina 27695-7905, USA
    J Biol Chem 278:37064-72. 2003
    ..Thus, at high concentrations of PDGF the kinetics of 3'-PI production are limited by the turnover rate of these lipids, while the Akt response is additionally influenced by the rate of Akt deactivation...
  12. ncbi Spontaneous phosphoinositide 3-kinase signaling dynamics drive spreading and random migration of fibroblasts
    Michael C Weiger
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695, USA
    J Cell Sci 122:313-23. 2009
    ..These results underscore the importance of localized PI3K signaling not only in chemotaxis but also in basal motility/migration of fibroblasts...
  13. ncbi A bipolar clamp mechanism for activation of Jak-family protein tyrosine kinases
    Dipak Barua
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA
    PLoS Comput Biol 5:e1000364. 2009
    ..Analysis of the results revealed a unique mechanism whereby SH2-B and receptor dimers constitute a bipolar 'clamp' that stabilizes the active configuration of two Jak2 molecules in the same macro-complex...
  14. ncbi Quantitative elucidation of a distinct spatial gradient-sensing mechanism in fibroblasts
    Ian C Schneider
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695, USA
    J Cell Biol 171:883-92. 2005
    ....
  15. ncbi On the cross-regulation of protein tyrosine phosphatases and receptor tyrosine kinases in intracellular signaling
    Jason M Haugh
    Department of Chemical Engineering, 113 Riddick Lab, Box 7905, North Carolina State University, Raleigh, NC 27695 7905, USA
    J Theor Biol 230:119-32. 2004
    ....
  16. ncbi Signal transduction at point-blank range: analysis of a spatial coupling mechanism for pathway crosstalk
    Michael I Monine
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Biophys J 95:2172-82. 2008
    ..We contend that this mechanism is a means by which signaling pathways are propagated and spatially coordinated for efficient crosstalk between them...
  17. ncbi Directional persistence of cell migration coincides with stability of asymmetric intracellular signaling
    Michael C Weiger
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, USA
    Biophys J 98:67-75. 2010
    ..These results are indicative of a mechanism by which changes in a cell's direction of migration are determined by a fragile balance of relatively rapid intracellular signaling processes...
  18. ncbi PI3K-dependent cross-talk interactions converge with Ras as quantifiable inputs integrated by Erk
    Chun Chao Wang
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695 7905, USA
    Mol Syst Biol 5:246. 2009
    ..Motivated by those dynamics, a kinetic model of the network was formulated and used to precisely quantify the relative contributions of PI3K-dependent and -independent modes of Ras/Erk activation...
  19. ncbi Stochastic model of integrin-mediated signaling and adhesion dynamics at the leading edges of migrating cells
    Murat Cirit
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina, United States of America
    PLoS Comput Biol 6:e1000688. 2010
    ....
  20. ncbi Mechanisms of gradient sensing and chemotaxis: conserved pathways, diverse regulation
    Ian C Schneider
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    Cell Cycle 5:1130-4. 2006
    ..The marked differences between this system and the others have led us to speculate on the diversity of gradient sensing mechanisms and their biological implications...
  21. ncbi Spatial analysis of 3' phosphoinositide signaling in living fibroblasts, III: influence of cell morphology and morphological Polarity
    Ian C Schneider
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, 27695, USA
    Biophys J 89:1420-30. 2005
    ..The morphological polarity of the cell may thus bias 3' PI signaling to promote persistent migration in fibroblasts...
  22. ncbi Computational models of tandem SRC homology 2 domain interactions and application to phosphoinositide 3-kinase
    Dipak Barua
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, North Carolina 27695, USA
    J Biol Chem 283:7338-45. 2008
    ..Homodimerization of full-length p85 was found to be an alternative mechanism for high avidity binding to phosphorylated platelet-derived growth factor receptors, which would render the N-SH2 domain dispensable for receptor binding...
  23. ncbi Quantitative model of Ras-phosphoinositide 3-kinase signalling cross-talk based on co-operative molecular assembly
    Harjeet Kaur
    Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC 27695-7905, USA
    Biochem J 393:235-43. 2006
    ....
  24. ncbi Biophysics: cells get in shape for a crawl
    Jason M Haugh
    Nature 453:461-2. 2008
  25. ncbi Membrane-binding/modification model of signaling protein activation and analysis of its control by cell morphology
    Jason M Haugh
    Biophys J 92:L93-5. 2007
    ..Moreover, this model allows for amplification of the activated protein bound at the membrane, which is considered more relevant for certain, spatially driven signaling processes in cell migration...

Research Grants6

  1. Molecular Crosstalk in Intracellular Signaling Netoworks
    JASON HAUGH; Fiscal Year: 2006
    ..Finally, for conditions found to perturb the signaling network, the corresponding effects on cell proliferation and survival will be assessed. ..
  2. Signal Transduction in Models of Fibroblast Invasion
    JASON HAUGH; Fiscal Year: 2007
    ..These efforts will serve as a foundation for more in-depth studies of molecular mechanisms governing physiological processes. ..
  3. Dynamic Regulation of Growth Factor Signaling Networks
    Jason M Haugh; Fiscal Year: 2010
    ..By analyzing these mechanisms quantitatively and using mathematical models, we hope to be able to predict the outcomes of interventions targeting the molecular players in these pathways. ..