A transistor model for the cystic fibrosis transmembrane conductance regulator

被引:0
作者
Hunt, William D. [1 ]
Mccarty, Nael A. [2 ]
Marin, Eduardo Martinez [1 ]
Westafer, Ryan S. [3 ]
Yamin, Phillip R. [1 ]
Cui, Guiying [2 ]
Eckford, Andrew W. [4 ]
Denison, Douglas R. [3 ]
机构
[1] Georgia Inst Technol, Atlanta, GA 30332 USA
[2] Emory Univ, Sch Med, Atlanta, GA USA
[3] GTRI, Atlanta, GA USA
[4] York Univ, Toronto, ON, Canada
来源
BIOPHYSICAL REPORTS | 2023年 / 3卷 / 02期
关键词
NUCLEOTIDE-BINDING DOMAIN; ATP-BINDING; BIOLOGICAL-MEMBRANES; IONIC CHANNELS; DELTA-F508; EQUATIONS; KINETICS; MURINE; CELLS; GENE;
D O I
10.1016/j.bpr.2023.100108
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this paper we present a transistor circuit model for cystic fibrosis transmembrane conductance regulator (CFTR) that seeks to map the functional form of CFTR both in wild type and mutants. The circuit architecture is configured so that the function, and as much as possible the form, faithfully represents what is known about CFTR from cryo-electron microscopy and molecular dynamics. The model is a mixed analog-digital topology with an AND gate receiving the input from two separate ATP-nucleotide-binding domain binding events. The analog portion of the circuit takes the output from the AND gate as its input. The input to the circuit model and its noise characteristics are extracted from single-channel patch-clamp experiments. The chloride current predicted by the model is then compared with single-channel patch-clamp re-cordings for wild-type CFTR. We also consider the patch-clamp recordings from CFTR with a G551D point mutation, a clinically relevant mutant that is responsive to therapeutic management. Our circuit model approach enables bioengineering ap-proaches to CFTR and allows biophysicists to use efficient circuit simulation tools to analyze its behavior.
引用
收藏
页数:13
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