XB-ART-59186
Nat Commun
2022 Jun 29;131:3760. doi: 10.1038/s41467-022-31526-7.
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Structural and electrophysiological basis for the modulation of KCNQ1 channel currents by ML277.
Willegems K
,
Eldstrom J
,
Kyriakis E
,
Ataei F
,
Sahakyan H
,
Dou Y
,
Russo S
,
Van Petegem F
,
Fedida D
.
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The KCNQ1 ion channel plays critical physiological roles in electrical excitability and K+ recycling in organs including the heart, brain, and gut. Loss of function is relatively common and can cause sudden arrhythmic death, sudden infant death, epilepsy and deafness. Here, we report cryogenic electron microscopic (cryo-EM) structures of Xenopus KCNQ1 bound to Ca2+/Calmodulin, with and without the KCNQ1 channel activator, ML277. A single binding site for ML277 was identified, localized to a pocket lined by the S4-S5 linker, S5 and S6 helices of two separate subunits. Several pocket residues are not conserved in other KCNQ isoforms, explaining specificity. MD simulations and point mutations support this binding location for ML277 in open and closed channels and reveal that prevention of inactivation is an important component of the activator effect. Our work provides direction for therapeutic intervention targeting KCNQ1 loss of function pathologies including long QT interval syndrome and seizures.
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???displayArticle.grants??? [+]
PJT-156181, PJT-175024 Gouvernement du Canada | Canadian Institutes of Health Research (Instituts de Recherche en Santé du Canada), RGPIN-2016-05422 Gouvernement du Canada | Natural Sciences and Engineering Research Council of Canada (Conseil de Recherches en Sciences Naturelles et en Génie du Canada), G-21-0031566 Heart and Stroke Foundation of Canada (Heart and Stroke Foundation), PJT-156181 CIHR, PJT-175024 CIHR, PJT 148632 CIHR
Genes referenced: kcnq1
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