| Authors |
Bianca J. van Lierop, Samuel D. Robinson, Shiva N. Kompella, Alessia Belgi,
Jeffrey R. McArthur, Andrew Hung, Christopher A. MacRaild, David J. Adams, Raymond S. Norton and Andrea J. Robinson |
| Published |
ACS Chemical Biology |
| Graphical abstract |
 |
| Abstract |
Conotoxins have emerged as useful leads for
the development of novel therapeutic analgesics. These peptides, isolated from marine molluscs of the genus Conus,
have evolved exquisite selectivity for receptors and ion
channels of excitable tissue. One such peptide, α-conotoxin
Vc1.1, is a 16-mer possessing an interlocked disulfide
framework. Despite its emergence as a potent analgesic lead,
the molecular target and mechanism of action of Vc1.1 have
not been elucidated to date. In this paper we describe the regioselective synthesis of dicarba analogues of Vc1.1 using olefin metathesis. The ability of these peptides to inhibit acetylcholine-evoked current at rat α9α10 and α3α4 nicotinic acetylcholine receptors (nAChR) expressed in Xenopus oocytes has been assessed in addition to their ability to inhibit high voltage-activated (HVA) calcium channel current in isolated rat DRG neurons. Their solution structures were determined by NMR spectroscopy. Significantly, we have found that regioselective replacement of the native cystine framework with a dicarba bridge can be used to selectively tune the cyclic peptide’s innate biological activity for one receptor over another. The 2,8-dicarba Vc1.1 isomer retains activity at γ-aminobutyric acid (GABAB) G protein-coupled receptors, whereas the isomeric 3,16-dicarba Vc1.1 peptide retains activity at the α9α10 nAChR subtype. These singularly acting analogues will enable the elucidation of the biological target responsible for the peptide’s potent analgesic activity. |
| Citation |
B. J. van Lierop, S. D. Robinson, S. N. Kompella, A. Belgi, J. R. McArthur, A. Hung, C. A. MacRaild, D. J. Adams, R. S. Norton, A. J. Robinson, ACS Chem. Biol., 2013, 8, 1815-1821. |
| Pdf |
Article |
| Doi |
DOI: 10.1021/cb4002393 |
| Related |
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Andrea Robinson Group 