Conorfamide-Sr3, a structurally novel specific inhibitor of the Shaker K+ channel. (November 2017)
- Record Type:
- Journal Article
- Title:
- Conorfamide-Sr3, a structurally novel specific inhibitor of the Shaker K+ channel. (November 2017)
- Main Title:
- Conorfamide-Sr3, a structurally novel specific inhibitor of the Shaker K+ channel
- Authors:
- Campos-Lira, Elba
Carrillo, Elisa
Aguilar, Manuel B.
Gajewiak, Joanna
Gómez-Lagunas, Froylán
López-Vera, Estuardo - Abstract:
- Abstract: Conorfamides (CNFs) are toxins initially characterized from the venom duct of the venomous marine snail Conus spurius from the Gulf of Mexico; at their C-termini, these toxins are amidated and have high sequence similarity with the molluskan cardioexcitatory tetrapeptide Phe-Met-Arg-Phe-NH2 (FMRFamide or FMRFa) and other FMRFa-related peptides (FaRPs) found in the five molluskan classes, and in other invertebrate and vertebrate phyla. These peptides were the first FaRPs found to be present in any venom, and they are biologically active in mice, limpets, and/or freshwater snails. However, the molecular targets of the known CNFs (CNF-Sr1 and CNF-Sr2 from C . spurius, and CNF-Vc1 from C . victoriae ) remain unidentified. Very recently, three FaRPs from C. textile have been found to potentiate the currents of acid-sensing ion channels. In this work, we characterized a novel conorfamide, CNF-Sr3 (ATSGPMGWLPVFYRF-NH2 ), comprised of 15 amino acid residues, and with a specific blocking activity for the Shaker subtype of the voltage-gated potassium channels, without significant effect on the Shab, Shaw, Shal and Eag channels. This peptide is the third type of disulfide-free conotoxins that has been discovered to target K + channels. Highlights: A novel conorfamide, CNF-Sr3, was discovered from the venom of Conus spurius . Among the voltage-gated potassium channels CNF-Sr3 blocks Shaker but not Shab, Shaw, Shal, and Eag . CNF-Sr3 is a new molecular tool for studying theAbstract: Conorfamides (CNFs) are toxins initially characterized from the venom duct of the venomous marine snail Conus spurius from the Gulf of Mexico; at their C-termini, these toxins are amidated and have high sequence similarity with the molluskan cardioexcitatory tetrapeptide Phe-Met-Arg-Phe-NH2 (FMRFamide or FMRFa) and other FMRFa-related peptides (FaRPs) found in the five molluskan classes, and in other invertebrate and vertebrate phyla. These peptides were the first FaRPs found to be present in any venom, and they are biologically active in mice, limpets, and/or freshwater snails. However, the molecular targets of the known CNFs (CNF-Sr1 and CNF-Sr2 from C . spurius, and CNF-Vc1 from C . victoriae ) remain unidentified. Very recently, three FaRPs from C. textile have been found to potentiate the currents of acid-sensing ion channels. In this work, we characterized a novel conorfamide, CNF-Sr3 (ATSGPMGWLPVFYRF-NH2 ), comprised of 15 amino acid residues, and with a specific blocking activity for the Shaker subtype of the voltage-gated potassium channels, without significant effect on the Shab, Shaw, Shal and Eag channels. This peptide is the third type of disulfide-free conotoxins that has been discovered to target K + channels. Highlights: A novel conorfamide, CNF-Sr3, was discovered from the venom of Conus spurius . Among the voltage-gated potassium channels CNF-Sr3 blocks Shaker but not Shab, Shaw, Shal, and Eag . CNF-Sr3 is a new molecular tool for studying the Shaker family. … (more)
- Is Part Of:
- Toxicon. Volume 138(2017)
- Journal:
- Toxicon
- Issue:
- Volume 138(2017)
- Issue Display:
- Volume 138, Issue 2017 (2017)
- Year:
- 2017
- Volume:
- 138
- Issue:
- 2017
- Issue Sort Value:
- 2017-0138-2017-0000
- Page Start:
- 53
- Page End:
- 58
- Publication Date:
- 2017-11
- Subjects:
- Conus spurius -- Mexico -- Conorfamide -- Ion channel blocker -- Potassium channels -- Shaker
Toxins -- Periodicals
Venom -- Periodicals
615.9 - Journal URLs:
- http://www.sciencedirect.com/science/journal/00410101 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.toxicon.2017.07.024 ↗
- Languages:
- English
- ISSNs:
- 0041-0101
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 8873.050000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4710.xml