TY - JOUR T1 - A functional NaV1.7-NavAb chimera with a reconstituted high affinity ProTx-II binding site JF - Molecular Pharmacology JO - Mol Pharmacol DO - 10.1124/mol.117.108712 SP - mol.117.108712 AU - Ramkumar Rajamani AU - Sophie Wu AU - Iyoncy Rodrigo AU - Mian Gao AU - Simon Low AU - Lisa Megson AU - David Wensel AU - Rick Pieschl AU - Debra Post-Munson AU - John Watson AU - David R Langley AU - Michael Ahlijanian AU - Linda Bristow AU - James Herrington Y1 - 2017/01/01 UR - http://molpharm.aspetjournals.org/content/early/2017/06/22/mol.117.108712.abstract N2 - NaV1.7 is genetically implicated in human pain perception. Rare gain of function mutations in NaV1.7 lead to spontaneous pain in humans whereas loss of function mutations result in congenital insensitivity to pain (CIP). Hence, agents that specifically modulate the function of NaV1.7 have the potential to yield novel therapeutics to treat pain. The complexity of the channel and the challenges to generate recombinant cell lines with high NaV1.7 expression have led to a templated target strategy approach employing chimeras with the bacterial channel, NavAb. In this report we describe the design, synthesis, purification and characterization of a chimera containing part of the voltage sensor domain 2 (VSD2) of NaV1.7. Importantly, this chimera, DII S1-S4, forms functional sodium channels and is potently inhibited by the NaV1.7 VSD2 targeted peptide toxin ProTx-II. Further, we show by [125I]ProTx-II binding and surface plasmon resonance (SPR) that the purified DII S1-S4 protein retains high affinity ProTx-II binding in detergent. We employed the purified DII S1-S4 protein to develop a scintillation proximity assay (SPA) suitable for high throughput screening. The creation of a NaV1.7-NavAb chimera with the VSD2 toxin binding site provides an important tool for the identification of novel NaV1.7 inhibitors and for structural studies to understand the toxin-channel interaction. ER -