A complicated complex: Ion channels, voltage sensing, cell membranes and peptide inhibitors

• Published in: Neuroscience letters 2018-07, Vol.679, p.35-47
• Main Authors: Zhang, Alan H., Sharma, Gagan, Undheim, Eivind A.B., Jia, Xinying, Mobli, Mehdi
• Format: Article
• Language: English
• Subjects: Cell membrane; Gating modifier toxins; Lipid binding; Receptor-ligand complex; Venom peptide; Voltage-gated ion channel
• ISSN: 0304-3940; 1872-7972
• DOI: 10.1016/j.neulet.2018.04.030

•Definition of voltage sensing voltage-gated ion channels.•The structure and gating cycle of voltage-gated ion channels.•Venom peptides that inhibit NaV1.7 by modulation of voltage sensing.•Channels that are likely off targets of NaV1.7-inhibiting peptides.•Kinetic models accounting for peptide:membrane interactions in channel inhibition. Voltage-gated ion channels (VGICs) are specialised ion channels that have a voltage dependent mode of action, where ion conduction, or gating, is controlled by a voltage-sensing mechanism. VGICs are critical for electrical signalling and are therefore important pharmacological targets. Among these, voltage-gated sodium channels (NaVs) have attracted particular attention as potential analgesic targets. NaVs, however, comprise several structurally similar subtypes with unique localisations and distinct functions, ranging from amplification of action potentials in nociception (e.g. NaV1.7) to controlling electrical signalling in cardiac function (NaV1.5). Understanding the structural basis of NaV function is therefore of great significance, both to our knowledge of electrical signalling and in development of subtype and state selective drugs. An important tool in this pursuit has been the use of peptides from animal venoms as selective NaV modulators. In this review, we look at peptides, particularly from spider venoms, that inhibit NaVs by binding to the voltage sensing domain (VSD) of this channel, known as gating modifier toxins (GMT). In the first part of the review, we look at the structural determinants of voltage sensing in VGICs, the gating cycle and the conformational changes that accompany VSD movement. Next, the modulation of the analgesic target NaV1.7 by GMTs is reviewed to develop bioinformatic tools that, based on sequence information alone, can identify toxins that are likely to inhibit this channel. The same approach is also used to define VSD sequences, other than that from NaV1.7, which are likely to be sensitive to this class of toxins. The final section of the review focuses on the important role of the cellular membrane in channel modulation and also how the lipid composition affects measurements of peptide-channel interactions both in binding kinetics measurements in solution and in cell-based functional assays.