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Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.

Cone snails are predatory creatures using venom as a weapon for prey capture and defense. Since this venom is neurotoxic, the venom gland is considered as an enormous collection of pharmacologically interesting compounds having a broad spectrum of targets. As such, cone snail peptides represent an i...

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Autores principales: Lebbe, Eline K. M., Ghequire, Maarten G. K., Peigneur, Steve, Mille, Bea G., Devi, Prabha, Ravichandran, Samuthirapandian, Waelkens, Etienne, D’Souza, Lisette, De Mot, René, Tytgat, Jan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128742/
https://www.ncbi.nlm.nih.gov/pubmed/27801785
http://dx.doi.org/10.3390/md14110199
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author Lebbe, Eline K. M.
Ghequire, Maarten G. K.
Peigneur, Steve
Mille, Bea G.
Devi, Prabha
Ravichandran, Samuthirapandian
Waelkens, Etienne
D’Souza, Lisette
De Mot, René
Tytgat, Jan
author_facet Lebbe, Eline K. M.
Ghequire, Maarten G. K.
Peigneur, Steve
Mille, Bea G.
Devi, Prabha
Ravichandran, Samuthirapandian
Waelkens, Etienne
D’Souza, Lisette
De Mot, René
Tytgat, Jan
author_sort Lebbe, Eline K. M.
collection PubMed
description Cone snails are predatory creatures using venom as a weapon for prey capture and defense. Since this venom is neurotoxic, the venom gland is considered as an enormous collection of pharmacologically interesting compounds having a broad spectrum of targets. As such, cone snail peptides represent an interesting treasure for drug development. Here, we report five novel peptides isolated from the venom of Conus longurionis, Conus asiaticus and Conus australis. Lo6/7a and Lo6/7b were retrieved from C. longurionis and have a cysteine framework VI/VII. Lo6/7b has an exceptional amino acid sequence because no similar conopeptide has been described to date (similarity percentage <50%). A third peptide, Asi3a from C. asiaticus, has a typical framework III Cys arrangement, classifying the peptide in the M-superfamily. Asi14a, another peptide of C. asiaticus, belongs to framework XIV peptides and has a unique amino acid sequence. Finally, AusB is a novel conopeptide from C. australis. The peptide has only one disulfide bond, but is structurally very different as compared to other disulfide-poor peptides. The peptides were screened on nAChRs, Na(V) and K(V) channels depending on their cysteine framework and proposed classification. No targets could be attributed to the peptides, pointing to novel functionalities. Moreover, in the quest of identifying novel pharmacological targets, the peptides were tested for antagonistic activity against a broad panel of Gram-negative and Gram-positive bacteria, as well as two yeast strains.
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spelling pubmed-51287422016-12-06 Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp. Lebbe, Eline K. M. Ghequire, Maarten G. K. Peigneur, Steve Mille, Bea G. Devi, Prabha Ravichandran, Samuthirapandian Waelkens, Etienne D’Souza, Lisette De Mot, René Tytgat, Jan Mar Drugs Article Cone snails are predatory creatures using venom as a weapon for prey capture and defense. Since this venom is neurotoxic, the venom gland is considered as an enormous collection of pharmacologically interesting compounds having a broad spectrum of targets. As such, cone snail peptides represent an interesting treasure for drug development. Here, we report five novel peptides isolated from the venom of Conus longurionis, Conus asiaticus and Conus australis. Lo6/7a and Lo6/7b were retrieved from C. longurionis and have a cysteine framework VI/VII. Lo6/7b has an exceptional amino acid sequence because no similar conopeptide has been described to date (similarity percentage <50%). A third peptide, Asi3a from C. asiaticus, has a typical framework III Cys arrangement, classifying the peptide in the M-superfamily. Asi14a, another peptide of C. asiaticus, belongs to framework XIV peptides and has a unique amino acid sequence. Finally, AusB is a novel conopeptide from C. australis. The peptide has only one disulfide bond, but is structurally very different as compared to other disulfide-poor peptides. The peptides were screened on nAChRs, Na(V) and K(V) channels depending on their cysteine framework and proposed classification. No targets could be attributed to the peptides, pointing to novel functionalities. Moreover, in the quest of identifying novel pharmacological targets, the peptides were tested for antagonistic activity against a broad panel of Gram-negative and Gram-positive bacteria, as well as two yeast strains. MDPI 2016-10-27 /pmc/articles/PMC5128742/ /pubmed/27801785 http://dx.doi.org/10.3390/md14110199 Text en © 2016 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Lebbe, Eline K. M.
Ghequire, Maarten G. K.
Peigneur, Steve
Mille, Bea G.
Devi, Prabha
Ravichandran, Samuthirapandian
Waelkens, Etienne
D’Souza, Lisette
De Mot, René
Tytgat, Jan
Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.
title Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.
title_full Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.
title_fullStr Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.
title_full_unstemmed Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.
title_short Novel Conopeptides of Largely Unexplored Indo Pacific Conus sp.
title_sort novel conopeptides of largely unexplored indo pacific conus sp.
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5128742/
https://www.ncbi.nlm.nih.gov/pubmed/27801785
http://dx.doi.org/10.3390/md14110199
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