<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Houston S</submitter><funding>Natural Sciences and Engineering Research Council of Canada</funding><funding>Social Sciences and Humanities Research Council of Canada</funding><funding>NIAID NIH HHS</funding><funding>Open Philanthropy Project</funding><funding>Division of Intramural Research</funding><funding>Canadian Institutes of Health Research</funding><pagination>1725-1743</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11077495</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>23(5)</volume><pubmed_abstract>Previous mass spectrometry (MS)-based global proteomics studies have detected a combined total of 86% of all &lt;i>Treponema pallidum&lt;/i> proteins under infection conditions (in vivo-grown &lt;i>T. pallidum&lt;/i>). Recently, a method was developed for the long-term culture of &lt;i>T. pallidum&lt;/i> under in vitro conditions (in vitro-cultured &lt;i>T. pallidum&lt;/i>). Herein, we used our previously reported optimized MS-based proteomics approach to characterize the &lt;i>T. pallidum&lt;/i> global protein expression profile under in vitro culture conditions. These analyses provided a proteome coverage of 94%, which extends the combined &lt;i>T. pallidum&lt;/i> proteome coverage from the previously reported 86% to a new combined total of 95%. This study provides a more complete understanding of the protein repertoire of</pubmed_abstract><journal>Journal of proteome research</journal><pubmed_title>In-Depth Proteome Coverage of In Vitro-Cultured &lt;i>Treponema pallidum&lt;/i> and Quantitative Comparison Analyses with In Vivo-Grown Treponemes.</pubmed_title><pmcid>PMC11077495</pmcid><funding_grant_id>R37AI051334</funding_grant_id><funding_grant_id>R37 AI051334</funding_grant_id><funding_grant_id>52345</funding_grant_id><funding_grant_id>U19AI144133</funding_grant_id><funding_grant_id>U19 AI144133</funding_grant_id><funding_grant_id>U01 AI182035</funding_grant_id><pubmed_authors>Goodyear MC</pubmed_authors><pubmed_authors>Geppert A</pubmed_authors><pubmed_authors>Cameron CE</pubmed_authors><pubmed_authors>Houston S</pubmed_authors><pubmed_authors>Gomez A</pubmed_authors></additional><is_claimable>false</is_claimable><name>In-Depth Proteome Coverage of In Vitro-Cultured &lt;i>Treponema pallidum&lt;/i> and Quantitative Comparison Analyses with In Vivo-Grown Treponemes.</name><description>Previous mass spectrometry (MS)-based global proteomics studies have detected a combined total of 86% of all &lt;i>Treponema pallidum&lt;/i> proteins under infection conditions (in vivo-grown &lt;i>T. pallidum&lt;/i>). Recently, a method was developed for the long-term culture of &lt;i>T. pallidum&lt;/i> under in vitro conditions (in vitro-cultured &lt;i>T. pallidum&lt;/i>). Herein, we used our previously reported optimized MS-based proteomics approach to characterize the &lt;i>T. pallidum&lt;/i> global protein expression profile under in vitro culture conditions. These analyses provided a proteome coverage of 94%, which extends the combined &lt;i>T. pallidum&lt;/i> proteome coverage from the previously reported 86% to a new combined total of 95%. This study provides a more complete understanding of the protein repertoire of</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 May</publication><modification>2026-06-03T06:50:51.698Z</modification><creation>2026-04-25T03:22:05.099Z</creation></dates><accession>S-EPMC11077495</accession><cross_references><pubmed>38636938</pubmed><doi>10.1021/acs.jproteome.3c00891</doi></cross_references></HashMap>