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Publication Abstract from PubMed

alpha-Conotoxins are peptide toxins found in the venom of marine cone snails and potent antagonists of various subtypes of nicotinic acetylcholine receptors (nAChRs). nAChRs are cholinergic receptors forming ligand-gated ion channels in the plasma membranes of certain neurons and the neuromuscular junction. Because nAChRs have an important role in regulating transmitter release, cell excitability, and neuronal integration, nAChR dysfunctions have been implicated in a variety of severe pathologies such as epilepsy, myasthenic syndromes, schizophrenia, Parkinson disease, and Alzheimer disease. To expand the knowledge concerning cone snail toxins, we examined the venom of Conus longurionis. We isolated an 18-amino acid peptide named alpha-conotoxin Lo1a, which is active on nAChRs. To the best of our knowledge, this is the first characterization of a conotoxin from this species. The peptide was characterized by electrophysiological screening against several types of cloned nAChRs expressed in Xenopus laevis oocytes. The three-dimensional solution structure of the alpha-conotoxin Lo1a was determined by NMR spectroscopy. Lo1a, a member of the alpha4/7 family, blocks the response to acetylcholine in oocytes expressing alpha7 nAChRs with an IC50 of 3.24 +/- 0.7 mum. Furthermore, Lo1a shows a high selectivity for neuronal versus muscle subtype nAChRs. Because Lo1a has an unusual C terminus, we designed two mutants, Lo1a-DeltaD and Lo1a-RRR, to investigate the influence of the C-terminal residue. Lo1a-DeltaD has a C-terminal Asp deletion, whereas in Lo1a-RRR, a triple-Arg tail replaces the Asp. They blocked the neuronal nAChR alpha7 with a lower IC50 value, but remarkably, both adopted affinity for the muscle subtype alpha1beta1deltaepsilon.

Structure-Function Elucidation of a New alpha-Conotoxin, Lo1a, from Conus longurionis.,Lebbe EK, Peigneur S, Maiti M, Devi P, Ravichandran S, Lescrinier E, Ulens C, Waelkens E, D'Souza L, Herdewijn P, Tytgat J J Biol Chem. 2014 Apr 4;289(14):9573-83. doi: 10.1074/jbc.M114.556175. Epub 2014 , Feb 24. PMID:24567324^[1]

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine.