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
[11]   Structural basis for the coupling between activation and inactivation gates in K+ channels [J].
Cuello, Luis G. ;
Jogini, Vishwanath ;
Cortes, D. Marien ;
Pan, Albert C. ;
Gagnon, Dominique G. ;
Dalmas, Olivier ;
Cordero-Morales, Julio F. ;
Chakrapani, Sudha ;
Roux, Benoit ;
Perozo, Eduardo .
NATURE, 2010, 466 (7303) :272-U154
[12]   Structural mechanism of C-type inactivation in K+ channels [J].
Cuello, Luis G. ;
Jogini, Vishwanath ;
Cortes, D. Marien ;
Perozo, Eduardo .
NATURE, 2010, 466 (7303) :203-U73
[13]   Permeation and Dynamics of an Open-Activated TRPV1 Channel [J].
Darre, Leonardo ;
Furini, Simone ;
Domene, Carmen .
JOURNAL OF MOLECULAR BIOLOGY, 2015, 427 (02) :537-549
[14]   NMRPIPE - A MULTIDIMENSIONAL SPECTRAL PROCESSING SYSTEM BASED ON UNIX PIPES [J].
DELAGLIO, F ;
GRZESIEK, S ;
VUISTER, GW ;
ZHU, G ;
PFEIFER, J ;
BAX, A .
JOURNAL OF BIOMOLECULAR NMR, 1995, 6 (03) :277-293
[15]   Tuning the ion selectivity of tetrameric cation channels by changing the number of ion binding sites [J].
Derebe, Mehabaw G. ;
Sauer, David B. ;
Zeng, Weizhong ;
Alam, Amer ;
Shi, Ning ;
Jiang, Youxing .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2011, 108 (02) :598-602
[16]   The structure of the potassium channel:: Molecular basis of K+ conduction and selectivity [J].
Doyle, DA ;
Cabral, JM ;
Pfuetzner, RA ;
Kuo, AL ;
Gulbis, JM ;
Cohen, SL ;
Chait, BT ;
MacKinnon, R .
SCIENCE, 1998, 280 (5360) :69-77
[17]   Gating at the Selectivity Filter of Ion Channels that Conduct Na+ and K+ Ions [J].
Furini, Simone ;
Domene, Carmen .
BIOPHYSICAL JOURNAL, 2011, 101 (07) :1623-1631
[18]   Mechanism of activation at the selectivity filter of the KcsA K+ channel [J].
Heer, Florian T. ;
Posson, David J. ;
Wojtas-Niziurski, Wojciech ;
Nimigean, Crina M. ;
Berneche, Simon .
ELIFE, 2017, 6
[19]   Sodium Ions Do Not Stabilize the Selectivity Filter of a Potassium Channel [J].
Hendriks, Kitty ;
Oester, Carl ;
Shi, Chaowei ;
Sun, Han ;
Lange, Adam .
JOURNAL OF MOLECULAR BIOLOGY, 2021, 433 (15)
[20]   Structural insights into the mechanisms of CNBD channel function [J].
James, Zachary M. ;
Zagotta, William N. .
JOURNAL OF GENERAL PHYSIOLOGY, 2018, 150 (02) :225-244