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

被引:0
作者
Matthew P. Harrigan
Keri A. McKiernan
Veerabahu Shanmugasundaram
Rajiah Aldrin Denny
Vijay S. Pande
机构
[1] Stanford University,Department of Chemistry
[2] Pfizer Inc.,Medicinal Sciences
[3] Pfizer Inc.,Medicinal Sciences
[4] Stanford University,Department of Computer Science
[5] Stanford University,Department of Structural Biology
[6] Stanford University,Program in Biophysics
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Scientific Reports | / 7卷
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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 μs 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.
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  • [1] Enyedi P(2010)Molecular background of leak k+ currents: Two-pore domain potassium channels Physiological Reviews 90 559-605
  • [2] Czirjak G(2000)Human trek2, a 2p domain mechano-sensitive k+ channel with multiple regulations by polyunsaturated fatty acids, lysophospholipids, and gs, gi, and gq protein-coupled receptors Journal of Biological Chemistry 275 28398-28405
  • [3] Lesage F(2011)Molecular regulations governing trek and traak channel functions Channels 5 402-409
  • [4] Terrenoire C(2016)Polymodal activation of the trek-2 k2p channel produces structurally distinct open states The Journal of general physiology 147 497-505
  • [5] Romey G(2001)Potassium leak channels and the kcnk family of two-p-domain subunits Nature Reviews Neuroscience 2 175-184
  • [6] Lazdunski M(2011)The pore structure and gating mechanism of k2p channels The EMBO journal 30 3607-3619
  • [7] Noël J(2012)State-independent intracellular access of quaternary ammonium blockers to the pore of trek-1 Channels 6 473-478
  • [8] Sandoz G(2015)K2p channel gating mechanisms revealed by structures of TREK-2 and a complex with prozac Science 347 1256-1259
  • [9] Lesage F(2009)Accelerating molecular dynamic simulation on graphics processing units J. Comput. Chem. 30 864-872
  • [10] McClenaghan C(2000)Screen savers of the world unite! Science 290 1903-1904