• DocumentCode
    3288269
  • Title

    Monotonicity and bistability of calcium/calmodulin-dependent protein kinase-phosphatase activation

  • Author

    Ming Wu ; Lawrence, D.A.

  • Author_Institution
    Sch. of Electr. Eng. & Comput. Sci., Ohio Univ., Athens, OH, USA
  • fYear
    2010
  • fDate
    June 30 2010-July 2 2010
  • Firstpage
    5923
  • Lastpage
    5928
  • Abstract
    Calcium/calmodulin-dependent protein kinase II (CaMKII) is thought to be a key contributor to the induction of long-term potentiation (LTP). Researchers have developed a variety of mathematical models of CaMKII activation intended to produce simulation output that agrees with empirical observations. This paper focuses on one such model to which recent theoretical results for input-output monotone systems are applied. Several key findings in the literature are reproduced using simple algebraic computations as opposed to exhaustive, simulation-based analysis. In particular, it is confirmed that bistability exists over a range of calcium concentrations that nominally includes the intracellular resting level and switching between high activation and low activation states is described by a hysteresis curve.
  • Keywords
    calcium; enzymes; mathematical analysis; molecular biophysics; bistability; calcium-calmodulin-dependent protein; hysteresis curve; input-output monotone systems; intracellular resting level; kinase-phosphatase activation; long-term potentiation; monotonicity; simulation-based analysis; switching; Analytical models; Biological control systems; Biological system modeling; Calcium; Computational modeling; Computer science; Hysteresis; Mathematical model; Nonlinear equations; Proteins;
  • fLanguage
    English
  • Publisher
    ieee
  • Conference_Titel
    American Control Conference (ACC), 2010
  • Conference_Location
    Baltimore, MD
  • ISSN
    0743-1619
  • Print_ISBN
    978-1-4244-7426-4
  • Type

    conf

  • DOI
    10.1109/ACC.2010.5531229
  • Filename
    5531229