hERG Function in Light of Structure.

Gail A Robertson, João H Morais-Cabral

Journal: Biophysical journal 2021;118(4):790-797

PMID: 31669064

Abstract

The human ether-a-go-go-related gene1 (hERG) ion channel has been the subject of fascination since it was identified as a target of long QT syndrome more than 20 years ago. In this Biophysical Perspective, we look at what makes hERG intriguing and vexingly unique. By probing recent high-resolution structures in the context of functional and biochemical data, we attempt to summarize new insights into hERG-specific function and articulate important unanswered questions. X-ray crystallography and cryo-electron microscopy have revealed features not previously on the radar-the "nonswapped" transmembrane architecture, an "intrinsic ligand," and hydrophobic pockets off a pore cavity that is surprisingly small. Advances in our understanding of drug block and inactivation mechanisms are noted, but a full picture will require more investigation.

Copyright © 2019 Biophysical Society. Published by Elsevier Inc. All rights reserved.

Address: Department of Neuroscience, School of Medicine and Public Health, University of Wisconsin-Madison, Madison, Wisconsin. Electronic address: [email protected].; i3S, Instituto de Investigação e Inovação em Saúde, Universidade do Porto, Porto, Portugal; IBMC- Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal.
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