Functional Expression in <em>Es</em><em>c</em><em>herichia coli</em> of the Disulfide-Rich Sea Anemone Peptide APETx2, a Potent Blocker of Acid-Sensing Ion Channel 3

Abstract

Acid-sensing ion channels (ASICs) are proton-gated sodium channels present in the central and peripheral nervous system of chordates. ASIC3 is highly expressed in sensory neurons and plays an important role in inflammatory and ischemic pain. Thus, specific inhibitors of ASIC3 have the potential to be developed as novel analgesics. APETx2, isolated from the sea anemone <em>Anthopleura elegantissima</em>,<em> </em>is the most potent and selective inhibitor of ASIC3-containing channels<em>.</em> However, the mechanism of action of APETx2 and the molecular basis for its interaction with ASIC3 is not known. In order to assist in characterizing the ASIC3-APETx2 interaction, we developed an efficient and cost-effective <em>Escherichia coli</em> periplasmic expression system for the production of APETx2. NMR studies on uniformly ¹³C/¹⁵N-labelled APETx2 produced in <em>E. coli</em> showed that the recombinant peptide adopts the native conformation. Recombinant APETx2 is equipotent with synthetic APETx2 at inhibiting ASIC3 channels expressed in <em>Xenopus</em> oocytes. Using this system we mutated Phe15 to Ala, which caused a profound loss of APETx2’s activity on ASIC3. These findings suggest that this expression system can be used to produce mutant versions of APETx2 in order to facilitate structure-activity relationship studies.

Keywords

• ASIC3
• APETx2
• heterologous expression
• NMR
• &lt;em&gt;E. coli&lt;/em&gt;