<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Debunne N</submitter><funding>Fonds Wetenschappelijk Onderzoek</funding><pagination>16120-16127</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7346264</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>5(26)</volume><pubmed_abstract>Finding adequate biomarkers for rapid and accurate disease detection, prognosis, and therapy is increasingly important. Quorum-sensing peptides are herein a new emerging group, produced by bacteria, fungi, protozoa, and viruses, with blood being the most straightforward sample type to detect/quantitate them. However, detailed information about suitable blood sample collection methods and storage conditions for measuring these quorum-sensing peptides hampers further clinical research and development. Here, we first tested the time-dependent stability of a set of chemically diverse quorum-sensing peptides, spiked in blood at different temperatures (4, 21, and 37 °C) in four different ethylenediamine tetraacetic acid (EDTA)-containing plasma tubes (with different protein-stabilizing additives</pubmed_abstract><journal>ACS omega</journal><pubmed_title>Influence of Blood Collection Methods and Long-Term Plasma Storage on Quorum-Sensing Peptide Stability.</pubmed_title><pmcid>PMC7346264</pmcid><funding_grant_id>1S21017N</funding_grant_id><funding_grant_id>1158818N</funding_grant_id><pubmed_authors>Debunne N</pubmed_authors><pubmed_authors>De Spiegeleer A</pubmed_authors><pubmed_authors>De Spiegeleer B</pubmed_authors><pubmed_authors>Depuydt D</pubmed_authors><pubmed_authors>Janssens Y</pubmed_authors><pubmed_authors>Descamps A</pubmed_authors><pubmed_authors>Wynendaele E</pubmed_authors></additional><is_claimable>false</is_claimable><name>Influence of Blood Collection Methods and Long-Term Plasma Storage on Quorum-Sensing Peptide Stability.</name><description>Finding adequate biomarkers for rapid and accurate disease detection, prognosis, and therapy is increasingly important. Quorum-sensing peptides are herein a new emerging group, produced by bacteria, fungi, protozoa, and viruses, with blood being the most straightforward sample type to detect/quantitate them. However, detailed information about suitable blood sample collection methods and storage conditions for measuring these quorum-sensing peptides hampers further clinical research and development. Here, we first tested the time-dependent stability of a set of chemically diverse quorum-sensing peptides, spiked in blood at different temperatures (4, 21, and 37 °C) in four different ethylenediamine tetraacetic acid (EDTA)-containing plasma tubes (with different protein-stabilizing additives</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Jul</publication><modification>2025-04-22T19:36:32.961Z</modification><creation>2025-04-06T02:47:03.555Z</creation></dates><accession>S-EPMC7346264</accession><cross_references><pubmed>32656434</pubmed><doi>10.1021/acsomega.0c01723</doi></cross_references></HashMap>