Bistability in the Ca2+/calmodulin-dependent protein kinase-phosphatase system

被引:125
作者
Zhabotinsky, AM
机构
[1] Brandeis Univ, Dept Chem, Waltham, MA 02454 USA
[2] Brandeis Univ, Volen Ctr Complex Syst, Waltham, MA 02454 USA
基金
美国国家科学基金会;
关键词
D O I
10.1016/S0006-3495(00)76469-1
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A mathematical model is presented of autophosphorylation of Ca2+/calmodulin-dependent protein kinase (CaMKII) and its dephosphorylation by a phosphatase. If the total concentration of CaMKII subunits is significantly higher than the phosphatase Michaelis constant, two stable steady states of the CaMKII autophosphorylation can exist in a Ca2+ concentration range from below the resting value of the intracellular [Ca2+] to the threshold concentration for induction of long-term potentiation (LTP). Bistability is a robust phenomenon, it occurs over a wide range of parameters of the model. Ca2+ transients that switch CaMKII from the low-phosphorylated state to the high-phosphorylated one are in the same range of amplitudes and frequencies as the Ca2+ transients that induce LTP. These results show that the CaMKII-phosphatase bistability may play an important role in long-term synaptic modifications. They also suggest a plausible explanation for the very high concentrations of CaMKII found in postsynaptic densities of cerebral neurons.
引用
收藏
页码:2211 / 2221
页数:11
相关论文
共 65 条
[61]   Protein phosphatase 1 is involved in the dissociation of Ca2+ calmodulin-dependent protein kinase II from postsynaptic densities [J].
Yoshimura, Y ;
Sogawa, Y ;
Yamauchi, T .
FEBS LETTERS, 1999, 446 (2-3) :239-242
[62]  
Yuste R, 1999, J NEUROSCI, V19, P1976
[63]  
Zhao WQ, 1999, J NEUROSCI RES, V55, P557, DOI 10.1002/(SICI)1097-4547(19990301)55:5<557::AID-JNR3>3.3.CO
[64]  
2-G
[65]   Enlightening the postsynaptic density [J].
Ziff, EB .
NEURON, 1997, 19 (06) :1163-1174