Ion-dependent structure, dynamics, and allosteric coupling in a non-selective cation channel

被引:9
作者
Lewis, Adam [1 ]
Kurauskas, Vilius [1 ]
Tonelli, Marco [2 ]
Henzler-Wildman, Katherine [1 ,2 ]
机构
[1] Univ Wisconsin, Dept Biochem, Madison, WI 53706 USA
[2] Univ Wisconsin, Natl Magnet Resonance Facil Madison NMRFAM, Madison, WI 53706 USA
基金
美国国家卫生研究院;
关键词
SELECTIVITY FILTER; NMR-SPECTROSCOPY; POTASSIUM-CHANNEL; MEMBRANE-PROTEINS; N-15; RELAXATION; K+; INACTIVATION; KCSA; PERMEATION; MECHANISMS;
D O I
10.1038/s41467-021-26538-8
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
NaK is a bacterial non-selective cation channel. Here, the authors use solution NMR to show that selectivity filter (SF) in NaK is dynamic, with structural differences between the Na+ and K + -bound states. The conformation of the SF is communicated to the pore-lining helices similarly as in the K + -selective channels. The selectivity filter (SF) determines which ions are efficiently conducted through ion channel pores. NaK is a non-selective cation channel that conducts Na+ and K+ with equal efficiency. Crystal structures of NaK suggested a rigid SF structure, but later solid-state NMR and MD simulations questioned this interpretation. Here, we use solution NMR to characterize how bound Na+ vs. K+ affects NaK SF structure and dynamics. We find that the extracellular end of the SF is flexible on the ps-ns timescale regardless of bound ion. On a slower timescale, we observe a structural change between the Na+ and K+-bound states, accompanied by increased structural heterogeneity in Na+. We also show direct evidence that the SF structure is communicated to the pore via I88 on the M2 helix. These results support a dynamic SF with multiple conformations involved in non-selective conduction. Our data also demonstrate allosteric coupling between the SF and pore-lining helices in a non-selective cation channel that is analogous to the allosteric coupling previously demonstrated for K+-selective channels, supporting the generality of this model.
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页数:11
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共 56 条
[21]   Fast time scale dynamics of protein backbones: NMR relaxation methods, applications, and functional consequences [J].
Jarymowycz, Virginia A. ;
Stone, Martin J. .
CHEMICAL REVIEWS, 2006, 106 (05) :1624-1671
[22]   Energetics of Ion Permeation in an Open-Activated TRPV1 Channel [J].
Jorgensen, Christian ;
Furini, Simone ;
Domene, Carmen .
BIOPHYSICAL JOURNAL, 2016, 111 (06) :1214-1222
[23]   Voltage-Gated Potassium Channels: A Structural Examination of Selectivity and Gating [J].
Kim, Dorothy M. ;
Nimigean, Crina M. .
COLD SPRING HARBOR PERSPECTIVES IN BIOLOGY, 2016, 8 (05)
[24]   Ion permeation in K+ channels occurs by direct Coulomb knock-on [J].
Koepfer, David A. ;
Song, Chen ;
Gruene, Tim ;
Sheldrick, George M. ;
Zachariae, Ulrich ;
de Groot, Bert L. .
SCIENCE, 2014, 346 (6207) :352-355
[25]   Molecular mechanism of a potassium channel gating through activation gate-selectivity filter coupling [J].
Kopec, Wojciech ;
Rothberg, Brad S. ;
de Groot, Bert L. .
NATURE COMMUNICATIONS, 2019, 10 (1)
[26]   Direct knock-on of desolvated ions governs strict ion selectivity in K+ channels [J].
Kopec, Wojciech ;
Koepfer, David A. ;
Vickery, Owen N. ;
Bondarenko, Anna S. ;
Jansen, Thomas L. C. ;
de Groot, Bert L. ;
Zachariae, Ulrich .
NATURE CHEMISTRY, 2018, 10 (08) :813-820
[27]   Probing slow dynamics in high molecular weight proteins by methyl-TROSY NMR spectroscopy: Application to a 723-residue enzyme [J].
Korzhnev, DM ;
Kloiber, K ;
Kanelis, V ;
Tugarinov, V ;
Kay, LE .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2004, 126 (12) :3964-3973
[28]   Instantaneous ion configurations in the K+ ion channel selectivity filter revealed by 2D IR spectroscopy [J].
Kratochvil, Huong T. ;
Carr, Joshua K. ;
Matulef, Kimberly ;
Annen, Alvin W. ;
Li, Hui ;
Maj, Michal ;
Ostmeyer, Jared ;
Serrano, Arnaldo L. ;
Raghuraman, H. ;
Moran, Sean D. ;
Skinner, J. L. ;
Perozo, Eduardo ;
Roux, Benoit ;
Valiyaveetil, Francis I. ;
Zanni, Martin T. .
SCIENCE, 2016, 353 (6303) :1040-1044
[29]   Structure of potassium channels [J].
Kuang, Qie ;
Purhonen, Pasi ;
Hebert, Hans .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2015, 72 (19) :3677-3693
[30]   Measurement of 15N relaxation rates in perdeuterated proteins by TROSY-based methods [J].
Lakomek, Nils-Alexander ;
Ying, Jinfa ;
Bax, Ad .
JOURNAL OF BIOMOLECULAR NMR, 2012, 53 (03) :209-221