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      <creatorName nameType="Personal">Rainsford, Philip</creatorName>
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      <creatorName nameType="Personal">Rylandsholm, Fredrik G.</creatorName>
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      <creatorName nameType="Personal">Jakubec, Martin</creatorName>
      <givenName>Martin</givenName>
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      <affiliation>UiT The Arctic University of Norway</affiliation>
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      <creatorName nameType="Personal">Silk, Mitchell</creatorName>
      <givenName>Mitchell</givenName>
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      <affiliation>UiT The Arctic University of Norway</affiliation>
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      <creatorName nameType="Personal">Juskewitz, Eric</creatorName>
      <givenName>Eric</givenName>
      <familyName>Juskewitz</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
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      <creatorName nameType="Personal">Ericson, Johanna U.</creatorName>
      <givenName>Johanna U.</givenName>
      <familyName>Ericson</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
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      <creatorName nameType="Personal">Svendsen, John S.</creatorName>
      <givenName>John S.</givenName>
      <familyName>Svendsen</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
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    <creator>
      <creatorName nameType="Personal">Engh, Richard A.</creatorName>
      <givenName>Richard A.</givenName>
      <familyName>Engh</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
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    <creator>
      <creatorName nameType="Personal">Isaksson, Johan</creatorName>
      <givenName>Johan</givenName>
      <familyName>Isaksson</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
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  <titles>
    <title>Supplementary Data for: Label-free measurement of antimicrobial peptide interactions with lipid vesicles and nanodiscs using microscale thermophoresis</title>
  </titles>
  <publisher>DataverseNO</publisher>
  <publicationYear>2023</publicationYear>
  <subjects>
    <subject>Chemistry</subject>
    <subject>Medicine, Health and Life Sciences</subject>
    <subject>SPR</subject>
    <subject>Surface Plasmon Resonance</subject>
    <subject>Microscale Thermophoresis</subject>
    <subject>MST</subject>
    <subject>Lipid nanodiscs</subject>
    <subject>antimicrobials</subject>
    <subject>Lipid vesicles</subject>
    <subject>binding affinity</subject>
  </subjects>
  <contributors>
    <contributor contributorType="Producer">
      <contributorName nameType="Organizational">UiT The Arctic University of Norway</contributorName>
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    <contributor contributorType="Distributor">
      <contributorName nameType="Organizational">UiT The Arctic University of Norway</contributorName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
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    <contributor contributorType="ContactPerson">
      <contributorName nameType="Personal">Jakubec, Martin</contributorName>
      <givenName>Martin</givenName>
      <familyName>Jakubec</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
    </contributor>
    <contributor contributorType="ContactPerson">
      <contributorName nameType="Personal">Rainsford, Philip</contributorName>
      <givenName>Philip</givenName>
      <familyName>Rainsford</familyName>
      <affiliation>UiT The Arctic University of Norway</affiliation>
    </contributor>
  </contributors>
  <dates>
    <date dateType="Created">2022-10-01</date>
    <date dateType="Submitted">2023-05-04</date>
    <date dateType="Available">2023-05-09</date>
    <date dateType="Updated">2023-09-28</date>
    <date dateType="Collected">2021-09-01/2022-09-30</date>
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    <description descriptionType="Abstract">This dataset contains raw data traces from Surface Plasmon Resonance (SPR) and Microscale Thermophoresis (MST) experiments aimed at determining the binding affinity of peptides with lipid vesicles and lipid nanodiscs. The SPR data consists of responses obtained from cycles of peptide injection over the lipid membrane, with varying peptide concentrations. The MST data includes fluorescence responses obtained from capillaries with different ratios of tested peptides and lipids. Tested hexapeptides were 1-c(WWWRRR), 2-c(WRWRWR), 3-c(WWWKKK), 4-c(WKWKWK) and 5-c(LWwNKr). The lipid compositions used in the experiments were pure 1,2-dimyristoyl-sn-glycero-3-phosphocholine (DMPC), DMPC with 5% (w/w) 1,2-dimyristoyl-sn-glycero-3-phospho-(1&amp;apos;-rac-glycerol) (DMPG), or DMPC with 10% (w/w) lipopolysaccharides from Escherichia coli O111:B4. These data traces are essential for measuring KP (lipid partitioning constant), understanding the peptide-lipid interaction and identifying potential candidates for further analysis.</description>
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      <funderName>Research Council of Norway</funderName>
      <awardNumber>DigiBiotics project - ID 269425</awardNumber>
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      <funderName>UiT the Arctic University of Norway</funderName>
      <awardNumber>AntiBioSpec project - Cristin ID 20161326</awardNumber>
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    <fundingReference>
      <funderName>Research Council of Norway</funderName>
      <awardNumber>NanoAMP project - ID 275186</awardNumber>
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