Chemical synthesis and folding of APETx2, a potent and selective inhibitor of acid sensing ion channel 3

Authors

Jonas Jensen, University of Queensland
Thomas Durek, University of Queensland
Paul F. Alewood, University of Queensland
David J. Adams, University of QueenslandFollow
Glenn F. King, University of Queensland
Lachlan D. Rash, University of Queensland

RIS ID

105543

Publication Details

Jensen, J. E., Durek, T., Alewood, P. F., Adams, D. J., King, G. F. & Rash, L. D. (2009). Chemical synthesis and folding of APETx2, a potent and selective inhibitor of acid sensing ion channel 3. Toxicon, 54 (1), 56-61.

Abstract

Acid sensing ion channels (ASICs) are pH-sensitive channels that are distributed in the central and peripheral nervous system and which are believed to play a key role in pain perception. APETx2, a 42-residue peptide toxin isolated from the sea anemone Anthopleura elegantissima, is the only known selective inhibitor of ASIC3 channels. Here we describe the total chemical synthesis of APETx2 by solid-phase peptide synthesis and native chemical ligation. The folded synthetic toxin had an IC50 of 57 nM for inhibition of rat ASIC3 channels expressed in Xenopus oocytes, in agreement with the IC50 reported for the native toxin (63 nM). The native chemical ligation approach should provide an efficient route for synthesis of other pharmacologically useful disulfide-rich toxins from venomous animals.