A governance of ion selectivity based on the occupancy of the "beacon" in one- and four-domain calcium and sodium channels

被引:0
作者
Spafford, J. David [1 ]
机构
[1] Univ Waterloo, Dept Biol, Waterloo, ON, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
Calcium channels; sodium channels; ion selectivity; AlphaFold2 molecular modeling; patch clamp; VOLTAGE-GATED SODIUM; UNION-OF-PHARMACOLOGY; T-TYPE CHANNELS; MOLECULAR-BASIS; PHARYNGEAL MUSCLE; CRYSTAL-STRUCTURE; SKELETAL-MUSCLE; INWARD CURRENTS; FROG-MUSCLE; BINDING;
D O I
10.1080/19336950.2023.2191773
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
One of nature's exceptions was discovered when a Cav3 T-type channel was observed to switch phenotype from a calcium channel into a sodium channel by neutralizing an aspartate residue in the high field strength (HFS) +1 position within the ion selectivity filter. The HFS+1 site is dubbed a "beacon" for its location at the entryway just above the constricted, minimum radius of the HFS site's electronegative ring. A classification is proposed based on the occupancy of the HFS+1 "beacon" which correlates with the calcium- or sodium-selectivity phenotype. If the beacon is a glycine, or neutral, non-glycine residue, then the cation channel is calcium-selective or sodium-permeable, respectively (Class I). Occupancy of a beacon aspartate are calcium-selective channels (Class II) or possessing a strong calcium block (Class III). A residue lacking in position of the sequence alignment for the beacon are sodium channels (Class IV). The extent to which animal channels are sodium-selective is dictated in the occupancy of the HFS site with a lysine residue (Class III/IV). Governance involving the beacon solves the quandary the HFS site as a basis for ion selectivity, where an electronegative ring of glutamates at the HFS site generates a sodium-selective channel in one-domain channels but generates a calcium-selective channel in four-domain channels. Discovery of a splice variant in an exceptional channel revealed nature's exploits, highlighting the "beacon" as a principal determinant for calcium and sodium selectivity, encompassing known ion channels composed of one and four domains, from bacteria to animals.
引用
收藏
页数:26
相关论文
共 100 条
[11]  
Bouza AA, 2018, HANDB EXP PHARMACOL, V246, P423, DOI 10.1007/164_2017_48
[12]   Evolutionary Genomics Reveals Lineage-Specific Gene Loss and Rapid Evolution of a Sperm-Specific Ion Channel Complex: CatSpers and CatSperβ [J].
Cai, Xinjiang ;
Clapham, David E. .
PLOS ONE, 2008, 3 (10)
[13]   International Union of Pharmacology. XLVII. Nomenclature and structure-function relationships of voltage-gated sodium channels [J].
Catterall, WA ;
Goldin, AL ;
Waxman, SG .
PHARMACOLOGICAL REVIEWS, 2005, 57 (04) :397-409
[14]  
Catterall WA, 2005, PHARMACOL REV, V57, P411, DOI 10.1124/pr.57.4.5
[15]   Ion Channel Voltage Sensors: Structure, Function, and Pathophysiology [J].
Catterall, William A. .
NEURON, 2010, 67 (06) :915-928
[16]   Multigene eukaryote phylogeny reveals the likely protozoan ancestors of opisthokonts (animals, fungi, choanozoans) and Amoebozoa [J].
Cavalier-Smith, Thomas ;
Chao, Ema E. ;
Snell, Elizabeth A. ;
Berney, Cedric ;
Fiore-Donno, Anna Maria ;
Lewis, Rhodri .
MOLECULAR PHYLOGENETICS AND EVOLUTION, 2014, 81 :71-85
[17]   Catalysis of Na+ permeation in the bacterial sodium channel NaVAb [J].
Chakrabarti, Nilmadhab ;
Ing, Christopher ;
Payandeh, Jian ;
Zheng, Ning ;
Catterall, William A. ;
Pomes, Regis .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2013, 110 (28) :11331-11336
[18]   NaChBac: The Long Lost Sodium Channel Ancestor [J].
Charalambous, Kalypso ;
Wallace, B. A. .
BIOCHEMISTRY, 2011, 50 (32) :6742-6752
[19]   Calmodulin regulates Cav3 T-type channels at their gating brake [J].
Chemin, Jean ;
Taiakina, Valentina ;
Monteil, Arnaud ;
Piazza, Michael ;
Guan, Wendy ;
Stephens, Robert F. ;
Kitmitto, Ashraf ;
Pang, Zhiping P. ;
Dolphin, Annette C. ;
Perez-Reyes, Edward ;
Dieckmann, Thorsten ;
Guillemette, Joseph Guy ;
Spafford, J. David .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2017, 292 (49) :20010-20031
[20]   CAVER 3.0: A Tool for the Analysis of Transport Pathways in Dynamic Protein Structures [J].
Chovancova, Eva ;
Pavelka, Antonin ;
Benes, Petr ;
Strnad, Ondrej ;
Brezovsky, Jan ;
Kozlikova, Barbora ;
Gora, Artur ;
Sustr, Vilem ;
Klvana, Martin ;
Medek, Petr ;
Biedermannova, Lada ;
Sochor, Jiri ;
Damborsky, Jiri .
PLOS COMPUTATIONAL BIOLOGY, 2012, 8 (10)