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The conductance of KCNQ2 and its pathogenic variants is determined by individual subunit gating

SCIENCE ADVANCES. 2025-03; 
Andy Hinojo-Perez, Jodene Eldstrom, Ying Dou, Allan Marinho-Alcara, Michaela A Edmond, Alicia de la Cruz, Marta E Perez Rodriguez, Maykelis Diaz-Solares, Derek M Dykxhoorn, David Fedida, Rene Barro-Soria University of Miami
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Gene Synthesis The full-length human KCNQ2 constructs (NCBI Reference Sequence: NP_742105.1; GenInfo Identifier: 26051264) and tandem dimers and tetramers of KCNQ2 (linkers in between subunits were composed of 25 glycine residues) were synthesized (GenScript USA, Piscataway, NJ) and ligated between the Bam HI and Xba I sites in the multiple cloning site into the pGEM-HE vector for oocyte expression or the pcDNA3.1 for mammalian cell expression. Get A Quote

摘要

KCNQ2 channel subunits form part of the M-current and underlie one of the major potassium currents throughout the human nervous system, regulating resting membrane potentials, shaping action potentials, and impeding repetitive neuronal firing. However, how individual subunits within tetramers control channel functionality remains unresolved. Here, we investigate (i) whether opening of KCNQ2 channels requires a concerted step or can result from independent subunit activation and (ii) how individual subunits regulate gate opening and conductance. The E140R mutation in the S2 segment prevents activated voltage sensor conformations, but concatemeric constructs containing up to three E140R subunits retain KCNQ2-like... More

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