<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Osipov AV</submitter><funding>Vietnamese Academy of Sciences and Technology</funding><funding>Russian Foundation for Basic Research</funding><pagination>1115</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10136136</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>11(4)</volume><pubmed_abstract>Protozoal infections are a world-wide problem. The toxicity and somewhat low effectiveness of the existing drugs require the search for new ways of protozoa suppression. Snake venom contains structurally diverse components manifesting antiprotozoal activity; for example, those in cobra venom are cytotoxins. In this work, we aimed to characterize a novel antiprotozoal component(s) in the &lt;i>Bungarus multicinctus&lt;/i> krait venom using the ciliate &lt;i>Tetrahymena pyriformis&lt;/i> as a model organism. To determine the toxicity of the substances under study, surviving ciliates were registered automatically by an original BioLaT-3.2 instrument. The krait venom was separated by three-step liquid chromatography and the toxicity of the obtained fractions against &lt;i>T. pyriformis&lt;/i> was analyzed. As a</pubmed_abstract><journal>Biomedicines</journal><pubmed_title>The Potassium Channel Blocker β-Bungarotoxin from the Krait &lt;i>Bungarus multicinctus&lt;/i> Venom Manifests Antiprotozoal Activity.</pubmed_title><pmcid>PMC10136136</pmcid><funding_grant_id>21-54-54005</funding_grant_id><funding_grant_id>QTRU01.15/21-22</funding_grant_id><pubmed_authors>Cheremnykh EG</pubmed_authors><pubmed_authors>Hoang AN</pubmed_authors><pubmed_authors>Starkov VG</pubmed_authors><pubmed_authors>Utkin YN</pubmed_authors><pubmed_authors>Nguyen TTT</pubmed_authors><pubmed_authors>Tsetlin VI</pubmed_authors><pubmed_authors>Osipov AV</pubmed_authors><pubmed_authors>Nguyen KC</pubmed_authors><pubmed_authors>Le DT</pubmed_authors><pubmed_authors>Ziganshin RH</pubmed_authors></additional><is_claimable>false</is_claimable><name>The Potassium Channel Blocker β-Bungarotoxin from the Krait &lt;i>Bungarus multicinctus&lt;/i> Venom Manifests Antiprotozoal Activity.</name><description>Protozoal infections are a world-wide problem. The toxicity and somewhat low effectiveness of the existing drugs require the search for new ways of protozoa suppression. Snake venom contains structurally diverse components manifesting antiprotozoal activity; for example, those in cobra venom are cytotoxins. In this work, we aimed to characterize a novel antiprotozoal component(s) in the &lt;i>Bungarus multicinctus&lt;/i> krait venom using the ciliate &lt;i>Tetrahymena pyriformis&lt;/i> as a model organism. To determine the toxicity of the substances under study, surviving ciliates were registered automatically by an original BioLaT-3.2 instrument. The krait venom was separated by three-step liquid chromatography and the toxicity of the obtained fractions against &lt;i>T. pyriformis&lt;/i> was analyzed. As a</description><dates><release>2023-01-01T00:00:00Z</release><publication>2023 Apr</publication><modification>2025-04-22T05:17:02.18Z</modification><creation>2025-04-05T21:16:51.698Z</creation></dates><accession>S-EPMC10136136</accession><cross_references><pubmed>37189733</pubmed><doi>10.3390/biomedicines11041115</doi></cross_references></HashMap>