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Mechanisms of KCNQ1 gating modulation by KCNE1/3 for cell-specific function

Chenxi Cui^1,† , Lu Zhao^2,† , Ali A. Kermani^3,† , Shuzong Du^2,† , Tanadet Pipatpolkai^4,5 , Meiqin Jiang¹ , Sagar Chittori³ , Yong Zi Tan¹ , Jingyi Shi² , Lucie Delemotte⁴ , Jianmin Cui^2,* , Ji Sun^1,*

¹Department of Biological Sciences, National University of Singapore, Singapore, Singapore
²Biomedical Engineering at Washington University in St. Louis, St. Louis, MO, USA
³Department of Structural Biology, St Jude Children’s Research Hospital, Memphis, TN, USA
⁴Department of Applied Physics, KTH Royal Institute of Technology, Stockholm, Sweden
⁵Present address: Division of Physics and Applied Physics, Nanyang Technological University, Singapore, Singapore
^†These authors contributed equally: Chenxi Cui, Lu Zhao, Ali A. Kermani, Shuzong Du
* Correspondence: Jianmin Cui(jcui@wustl.edu)Ji Sun(jsun1@nus.edu.sg)

KCNQ1 potassium channels are essential for physiological processes such as cardiac rhythm and intestinal chloride secretion. KCNE family subunits (KCNE1–5) associate with KCNQ1, conferring distinct properties across various tissues. KCNQ1 activation requires membrane depolarization and phosphatidylinositol 4,5-bisphosphate (PIP2) whose cellular levels are controlled by Gαq-coupled GPCR activation. While modulation of KCNQ1’s voltage-dependent activation by KCNE1/3 is well-characterized, their effects on PIP2-dependent gating of KCNQ1 via GPCR signaling remain less understood. Here we resolved structures of KCNQ1–KCNE1 and reassessed the reported KCNQ1–KCNE3 structures with and without PIP2. We revealed that KCNQ1–KCNE1/3 complexes feature two PIP2-binding sites, with KCNE1/3 contributing to a previously overlooked, uncharacterized site involving residues critical for coupling voltage sensor and pore domains. Via this site, KCNE1 and KCNE3 distinctly modulate the PIP2-dependent gating, in addition to the voltage sensitivity, of KCNQ1. Consequently, KCNE3 converts KCNQ1 into a voltage-insensitive PIP2-gated channel governed by GPCR signaling to maintain ion homeostasis in non-excitable cells. KCNE1, by significantly enhancing KCNQ1’s PIP2 affinity and resistance to GPCR regulation, forms predominantly voltage-gated channels with KCNQ1 for conducting the slow-delayed rectifier current in excitable cardiac cells. Our study highlights how KCNE1/3 modulates KCNQ1 gating in different cellular contexts, providing insights into tissue-specifically targeting multi-functional channels.

https://doi.org/10.1038/s41422-025-01152-1

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