<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>16</volume><submitter>Antunes A</submitter><pubmed_abstract>The venom of &lt;i>Cyriopagopus schmidti&lt;/i> spider has been extensively investigated, thereby allowing the identification of numerous new natural peptides. Many of these peptides are active on ion channels and several of them occur from post-translational processing. In order to further identify new entities, we screened this venom against five different human voltage-gated sodium (hNa&lt;sub>v&lt;/sub>) channels. We illustrate the unusual richness of this venom in targeting this wide variety of hNa&lt;sub>v&lt;/sub> channels. We confirm the identity of previously discovered peptides active on these ion channels type (huwentoxin (HwTx)-I, HwTx-II and HwTx-IV), indicating the efficacy of the screening process by automated patch-clamp. We also identified a novel analogue of HwTx-IV that differs by the abs</pubmed_abstract><journal>Frontiers in pharmacology</journal><pagination>1566312</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC12019880</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>The venom of &amp;lt;i&amp;gt;Cyriopagopus schmidti&amp;lt;/i&amp;gt; spider contains a natural huwentoxin-IV analogue with unexpected improved analgesic potential.</pubmed_title><pmcid>PMC12019880</pmcid><pubmed_authors>De Waard M</pubmed_authors><pubmed_authors>Benoit E</pubmed_authors><pubmed_authors>Servent D</pubmed_authors><pubmed_authors>Lopez L</pubmed_authors><pubmed_authors>Thomas B</pubmed_authors><pubmed_authors>Antunes A</pubmed_authors><pubmed_authors>Ribeiro Oliveira-Mendes B</pubmed_authors><pubmed_authors>Jaquillard L</pubmed_authors><pubmed_authors>Khakh K</pubmed_authors><pubmed_authors>Montnach J</pubmed_authors><pubmed_authors>Cohen CJ</pubmed_authors><pubmed_authors>Beroud R</pubmed_authors></additional><is_claimable>false</is_claimable><name>The venom of &amp;lt;i&amp;gt;Cyriopagopus schmidti&amp;lt;/i&amp;gt; spider contains a natural huwentoxin-IV analogue with unexpected improved analgesic potential.</name><description>The venom of &lt;i>Cyriopagopus schmidti&lt;/i> spider has been extensively investigated, thereby allowing the identification of numerous new natural peptides. Many of these peptides are active on ion channels and several of them occur from post-translational processing. In order to further identify new entities, we screened this venom against five different human voltage-gated sodium (hNa&lt;sub>v&lt;/sub>) channels. We illustrate the unusual richness of this venom in targeting this wide variety of hNa&lt;sub>v&lt;/sub> channels. We confirm the identity of previously discovered peptides active on these ion channels type (huwentoxin (HwTx)-I, HwTx-II and HwTx-IV), indicating the efficacy of the screening process by automated patch-clamp. We also identified a novel analogue of HwTx-IV that differs by the abs</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025</publication><modification>2025-06-26T03:05:27.25Z</modification><creation>2025-06-26T03:05:27.25Z</creation></dates><accession>S-EPMC12019880</accession><cross_references><pubmed>40276610</pubmed><doi>10.3389/fphar.2025.1566312</doi></cross_references></HashMap>