Markov modeling reveals novel intracellular modulation of the human TREK-2 selectivity filter

被引:14
|
作者
Harrigan, Matthew P. [1 ]
McKiernan, Keri A. [1 ]
Shanmugasundaram, Veerabahu [2 ]
Denny, Rajiah Aldrin [3 ]
Pande, Vijay S. [1 ,4 ,5 ,6 ]
机构
[1] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
[2] Pfizer Inc, Med Sci, Eastern Point Rd, Groton, CT 06340 USA
[3] Pfizer Inc, Med Sci, 610 Main St, Cambridge, MA 02139 USA
[4] Stanford Univ, Dept Comp Sci, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Biol Struct, Stanford, CA 94305 USA
[6] Stanford Univ, Program Biophys, Stanford, CA 94305 USA
来源
SCIENTIFIC REPORTS | 2017年 / 7卷
基金
美国国家科学基金会;
关键词
K+ CHANNELS; REGULATIONS; LIBRARY; OPENMM; AMBER;
D O I
10.1038/s41598-017-00256-y
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
Two-pore domain potassium (K2P) channel ion conductance is regulated by diverse stimuli that directly or indirectly gate the channel selectivity filter (SF). Recent crystal structures for the TREK-2 member of the K2P family reveal distinct "up" and "down" states assumed during activation via mechanical stretch. We performed 195 mu s of all-atom, unbiased molecular dynamics simulations of the TREK-2 channel to probe how membrane stretch regulates the SF gate. Markov modeling reveals a novel "pinched" SF configuration that stretch activation rapidly destabilizes. Free-energy barrier heights calculated for critical steps in the conduction pathway indicate that this pinched state impairs ion conduction. Our simulations predict that this low-conductance state is accessed exclusively in the compressed, "down" conformation in which the intracellular helix arrangement allosterically pinches the SF. By explicitly relating structure to function, we contribute a critical piece of understanding to the evolving K2P puzzle.
引用
收藏
页数:8
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