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Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a

Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5247677

Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a

About this item

Full title

Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a

Publisher

London: Nature Publishing Group UK

Journal title

Scientific reports, 2017-01, Vol.7 (1), p.40883-40883, Article 40883

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Human genetic studies have implicated the voltage-gated sodium channel Na
V
1.7 as a therapeutic target for the treatment of pain. A novel peptide, μ-theraphotoxin-Pn3a, isolated from venom of the tarantula
Pamphobeteus nigricolor,
potently inhibits Na
V
1.7 (IC
50
0.9 nM) with at least 40–1000-fold selectivity over all othe...

Alternative Titles

Full title

Pharmacological characterisation of the highly NaV1.7 selective spider venom peptide Pn3a

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5247677

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5247677

Other Identifiers

ISSN

2045-2322

E-ISSN

2045-2322

DOI

10.1038/srep40883

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