Mutagenesis of α-Conotoxins for Enhancing Activity and Selectivity for Nicotinic Acetylcholine Receptors

• Main Authors: Matthew W. Turner, Leanna A. Marquart, Paul D. Phillips, Owen M. McDougal
• Format: Article
• Language: English
• Published: MDPI AG 2019-02-01
• Series: Toxins
• Subjects: α-conotoxins (α-CTxs); nicotinic acetylcholine receptors (nAChRs); mutational analysis; positional scanning synthetic combinatorial libraries (PS-SCL); acetylcholine binding protein (AChBP); protein surface topography (PST); genetic algorithm managed peptide mutant screening (GAMPMS); molecular dynamics (MD); solid phase peptide synthesis (SPPS)
• Online Access: https://www.mdpi.com/2072-6651/11/2/113

Nicotinic acetylcholine receptors (nAChRs) are found throughout the mammalian body and have been studied extensively because of their implication in a myriad of diseases. &#945;-Conotoxins (&#945;-CTxs) are peptide neurotoxins found in the venom of marine snails of genus <i>Conus</i>. &#945;-CTxs are potent and selective antagonists for a variety of nAChR isoforms. Over the past 40 years, &#945;-CTxs have proven to be valuable molecular probes capable of differentiating between closely related nAChR subtypes and have contributed greatly to understanding the physiological role of nAChRs in the mammalian nervous system. Here, we review the amino acid composition and structure of several &#945;-CTxs that selectively target nAChR isoforms and explore strategies and outcomes for introducing mutations in native &#945;-CTxs to direct selectivity and enhance binding affinity for specific nAChRs. This review will focus on structure-activity relationship studies involving native &#945;-CTxs that have been rationally mutated and molecular interactions that underlie binding between ligand and nAChR isoform.