Cargando…
Peptide ion channel toxins from the bootlace worm, the longest animal on Earth
Polypeptides from animal venoms have found important uses as drugs, pharmacological tools, and within biotechnological and agricultural applications. We here report a novel family of cystine knot peptides from nemertean worms, with potent activity on voltage-gated sodium channels. These toxins, name...
Autores principales: | , , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2018
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864730/ https://www.ncbi.nlm.nih.gov/pubmed/29567943 http://dx.doi.org/10.1038/s41598-018-22305-w |
_version_ | 1783308541709254656 |
---|---|
author | Jacobsson, Erik Andersson, Håkan S. Strand, Malin Peigneur, Steve Eriksson, Camilla Lodén, Henrik Shariatgorji, Mohammadreza Andrén, Per E. Lebbe, Eline K. M. Rosengren, K. Johan Tytgat, Jan Göransson, Ulf |
author_facet | Jacobsson, Erik Andersson, Håkan S. Strand, Malin Peigneur, Steve Eriksson, Camilla Lodén, Henrik Shariatgorji, Mohammadreza Andrén, Per E. Lebbe, Eline K. M. Rosengren, K. Johan Tytgat, Jan Göransson, Ulf |
author_sort | Jacobsson, Erik |
collection | PubMed |
description | Polypeptides from animal venoms have found important uses as drugs, pharmacological tools, and within biotechnological and agricultural applications. We here report a novel family of cystine knot peptides from nemertean worms, with potent activity on voltage-gated sodium channels. These toxins, named the α-nemertides, were discovered in the epidermal mucus of Lineus longissimus, the ‘bootlace worm’ known as the longest animal on earth. The most abundant peptide, the 31-residue long α-1, was isolated, synthesized, and its 3D NMR structure determined. Transcriptome analysis including 17 species revealed eight α-nemertides, mainly distributed in the genus Lineus. α-1 caused paralysis and death in green crabs (Carcinus maenas) at 1 µg/kg (~300 pmol/kg). It showed profound effect on invertebrate voltage-gated sodium channels (e.g. Blattella germanica Na(v)1) at low nanomolar concentrations. Strong selectivity for insect over human sodium channels indicates that α-nemertides can be promising candidates for development of bioinsecticidal agents. |
format | Online Article Text |
id | pubmed-5864730 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-58647302018-03-27 Peptide ion channel toxins from the bootlace worm, the longest animal on Earth Jacobsson, Erik Andersson, Håkan S. Strand, Malin Peigneur, Steve Eriksson, Camilla Lodén, Henrik Shariatgorji, Mohammadreza Andrén, Per E. Lebbe, Eline K. M. Rosengren, K. Johan Tytgat, Jan Göransson, Ulf Sci Rep Article Polypeptides from animal venoms have found important uses as drugs, pharmacological tools, and within biotechnological and agricultural applications. We here report a novel family of cystine knot peptides from nemertean worms, with potent activity on voltage-gated sodium channels. These toxins, named the α-nemertides, were discovered in the epidermal mucus of Lineus longissimus, the ‘bootlace worm’ known as the longest animal on earth. The most abundant peptide, the 31-residue long α-1, was isolated, synthesized, and its 3D NMR structure determined. Transcriptome analysis including 17 species revealed eight α-nemertides, mainly distributed in the genus Lineus. α-1 caused paralysis and death in green crabs (Carcinus maenas) at 1 µg/kg (~300 pmol/kg). It showed profound effect on invertebrate voltage-gated sodium channels (e.g. Blattella germanica Na(v)1) at low nanomolar concentrations. Strong selectivity for insect over human sodium channels indicates that α-nemertides can be promising candidates for development of bioinsecticidal agents. Nature Publishing Group UK 2018-03-22 /pmc/articles/PMC5864730/ /pubmed/29567943 http://dx.doi.org/10.1038/s41598-018-22305-w Text en © The Author(s) 2018 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Jacobsson, Erik Andersson, Håkan S. Strand, Malin Peigneur, Steve Eriksson, Camilla Lodén, Henrik Shariatgorji, Mohammadreza Andrén, Per E. Lebbe, Eline K. M. Rosengren, K. Johan Tytgat, Jan Göransson, Ulf Peptide ion channel toxins from the bootlace worm, the longest animal on Earth |
title | Peptide ion channel toxins from the bootlace worm, the longest animal on Earth |
title_full | Peptide ion channel toxins from the bootlace worm, the longest animal on Earth |
title_fullStr | Peptide ion channel toxins from the bootlace worm, the longest animal on Earth |
title_full_unstemmed | Peptide ion channel toxins from the bootlace worm, the longest animal on Earth |
title_short | Peptide ion channel toxins from the bootlace worm, the longest animal on Earth |
title_sort | peptide ion channel toxins from the bootlace worm, the longest animal on earth |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5864730/ https://www.ncbi.nlm.nih.gov/pubmed/29567943 http://dx.doi.org/10.1038/s41598-018-22305-w |
work_keys_str_mv | AT jacobssonerik peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT anderssonhakans peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT strandmalin peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT peigneursteve peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT erikssoncamilla peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT lodenhenrik peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT shariatgorjimohammadreza peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT andrenpere peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT lebbeelinekm peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT rosengrenkjohan peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT tytgatjan peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth AT goranssonulf peptideionchanneltoxinsfromthebootlacewormthelongestanimalonearth |