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Structure-function elucidation of a new alpha-Conotoxin, Lo1a, from Conus longurionis.

DRS at CSIR-National Institute of Oceanography

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Title Structure-function elucidation of a new alpha-Conotoxin, Lo1a, from Conus longurionis.
 
Creator Lebbe, E.K.M.
Peigneur, S.
Maiti, M.
PrabhaDevi
Ravichandran, S.
Lescrinier, E.
Ulens, C.
Waelkens, E.
DeSouza, L.
Herdewijn, P.
Tytgat, J.
 
Subject marine cone snails
peptide toxins
 
Description 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 ~k M. Furthermore, Lo1a shows a high selectivity for neuronal versus muscle subtype nAChRs. Because Lo1a has an unusual C terminus, we designed two mutants, Lo1a-~n D and Lo1a-RRR, to investigate the influence of the C-terminal residue. Lo1a-~n D has a C-terminal Asp deletion, whereas in Lo1a-RRR, a triple-Arg tail replaces the Asp. They blocked the neuronal nAChR Alpha 7 with a lower IC50 value, but remarkably, both adopted affinity for the muscle subtype Alpha1 Beta1 delta ~e.
 
Date 2014-06-11T11:23:51Z
2014-06-11T11:23:51Z
2014
 
Type Journal Article
 
Identifier Journal of Biological Chemistry, vol.289(14); 2014; 9573-9583
http://drs.nio.org/drs/handle/2264/4537
 
Language en
 
Rights "This research was originally published in Journal Of Biological Chemistry, vol.289(14); 2014; 9573-9583. © the American Society for Biochemistry and Molecular Biology."
 
Publisher American Society for Biochemistry and Molecular Biology