A state-mutating genetic algorithm to design ion-channel models

被引:36
|
作者
Menon, Vilas [1 ]
Spruston, Nelson [2 ]
Kath, William L. [1 ,2 ,3 ]
机构
[1] Northwestern Univ, McCormick Sch Engn, Evanston, IL 60208 USA
[2] Northwestern Univ, Weinberg Coll Arts & Sci, Evanston, IL 60208 USA
[3] Northwestern Univ, Northwestern Inst Complex Syst, Evanston, IL 60208 USA
基金
美国国家卫生研究院;
关键词
ACTION-POTENTIALS; SINGLE-CHANNEL; SLOW INACTIVATION; NA+ CHANNELS; SODIUM; ATTENUATION; CURRENTS; NEURONS; DENDRITES; KINETICS;
D O I
10.1073/pnas.0903766106
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Realistic computational models of single neurons require component ion channels that reproduce experimental findings. Here, a topology-mutating genetic algorithm that searches for the best state diagram and transition-rate parameters to model macroscopic ion-channel behavior is described. Important features of the algorithm include a topology-altering strategy, automatic satisfaction of equilibrium constraints (microscopic reversibility), and multiple-protocol fitting using sequential goal programming rather than explicit weighting. Application of this genetic algorithm to design a sodium-channel model exhibiting both fast and prolonged inactivation yields a six-state model that produces realistic activity-dependent attenuation of action-potential backpropagation in current-clamp simulations of a CA1 pyramidal neuron.
引用
收藏
页码:16829 / 16834
页数:6
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