Modulatory features of the novel spider toxin μ-TRTX-Df1a isolated from the venom of the spider Davus fasciatus. Running title: Modulation of voltage-gated channels by the spider toxin Df1a Fernanda C Cardosoa*, Zoltan Dekana, Jennifer J Smitha, Jennifer R Deuisa,b, Irina Vettera,b, Volker Herziga, Paul F Alewooda, Glenn F Kinga and Richard J. Lewisa*. aInstitute for Molecular Bioscience, The University of Queensland, St Lucia, Qld 4072, AU. bSchool of Pharmacy, The University of Queensland, Woolloongabba, Qld 4102, AU. Corresponding authors*: Prof Richard J. Lewis, 306 Carmody Rd, St Lucia, Qld 4072, Australia. Phone: +61 7 3346 2984, e-mail:
[email protected]; Dr Fernanda C. Cardoso, 306 Carmody Rd, St Lucia, Qld 4072, Australia. Phone: +61 7 3346 2986, e-mail:
[email protected]. Number of figures: 9 Number of tables: 1 Supporting information: 3 This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process which may lead to differences between this version and the Version of Record. Please cite this article as doi: 10.1111/bph.13865 This article is protected by copyright. All rights reserved. Abstract Background and purpose Naturally occurring dysfunction in NaV channels results in complex disorders such as chronic pain, making these channels an attractive target for new therapies. In the pursuit of novel NaV modulators, we investigated spider venoms for new inhibitors of NaV channels. Experimental Approach We used high-throughput screens to identify a NaV modulator in venom of the spider Davus fasciatus.