Can I read Structural basis for NaV1.7 inhibition by pore blockers on EtoBox?

Structural basis for NaV1.7 inhibition by pore blockers by Jiangtao Zhang; Yiqiang Shi; Zhuo Huang; Yue Li; Bei Yang; Jianke Gong; Daohua Jiang is a Biochemistry, Genetics and Molecular Biology article available to read on EtoBox.

What is Structural basis for NaV1.7 inhibition by pore blockers about?

Voltage-gated sodium channel Na V 1.7 plays essential roles in pain and odor perception. Na V 1.7 variants cause pain disorders. Accordingly, Na V 1.7 has elicited extensive attention in developing new analgesics. Here we present cryo-EM structures of human Na V 1.7/β1/β2 complexed with inhibitors XEN907, TC-N1752 and Na V 1.7-IN2, explaining specific binding sites and modulation mechanism for the pore blockers. These inhibitors bind in the central cavity blocking ion permeation, but engage different parts of the cavity wall. XEN907 directly causes α-to π-helix transition of DIV-S6 helix, which tightens the fast inactivation gate. TC-N1752 induces π-helix transition of DII-S6 helix mediated by a conserved asparagine on DIII-S6, which closes the activation gate. Na V 1.7-IN2 serves as a pore blocker without causing conformational change. Electrophysiological results demonstrate that XEN907 and TC-N1752 stabilize Na V 1.7 in inactivated state and delay the recovery from inactivation. Our results provide structural framework for Na V 1.7 modulation by pore blockers, and important implications for developing subtype-selective analgesics.Voltage-gated sodium (Na V ) channels play fundam

Who reads Structural basis for NaV1.7 inhibition by pore blockers?

Author

Jiangtao Zhang; Yiqiang Shi; Zhuo Huang; Yue Li; Bei Yang; Jianke Gong; Daohua Jiang

Publisher

Springer Science and Business Media LLC

Published

2022

Language

EN

Field

Biochemistry, Genetics and Molecular Biology (Life Sciences)