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        <identifier>oai:figshare.com:article/32641902</identifier>
        <datestamp>2026-10-01T16:19:52Z</datestamp>
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          <dc:title>Identification and functional study of a bioactive peptide, QUB-2323, from the skin secretion of the orange-legged monkey tree frog, &lt;i&gt;Phyllomedusa azurea&lt;/i&gt;</dc:title>
          <dc:creator>Yue Tang (235893)</dc:creator>
          <dc:subject>PUREID: 658700942</dc:subject>
          <dc:subject>AMPs</dc:subject>
          <dc:subject>dermaseptin</dc:subject>
          <dc:subject>antimicrobial activity</dc:subject>
          <dc:subject>anti-proliferative activity</dc:subject>
          <dc:subject>toxicity</dc:subject>
          <dc:description>The widespread use of antibiotics has contributed significantly to the emergence of bacterial resistance. Antimicrobial peptides (AMPs) have emerged as promising antibacterial drug candidates due to their broad-spectrum of activity and low potential for resistance development. In this study, the precursor cDNA encoding an AMP, named QUB-2323, was isolated from the skin secretion of the orange-legged monkey tree frog, Phyllomedusa azurea, using shotgun cloning. Sequence analysis identified QUB-2323 as a member of the Dermaseptin family of AMPs, with the mature peptide sequence of GLWSTIKNVGKEAAIAAGKAALGAL-amide. &lt;br&gt;&lt;br&gt;A series of experiments was conducted to evaluate the biological activity of QUB-2323. The peptide displayed broad-spectrum antimicrobial activity, with minimum inhibitory concentrations (MICs) of 1 µM against Staphylococcus aureus (NCTC 10788) and Candida albicans (NCYC 1467), and 0.5 µM against Escherichia coli (NCTC 10418). QUB-2323 also exhibited anti-proliferative activity, with an IC50 value of 6.44 µM against the lung cancer cell line, NCI-H838. However, the peptide showed notable cytotoxicity: a haemolytic concentration (HC₅₀) of approximately 128 µM against horse erythrocytes and an IC₅₀ of 2.377 µM against normal human lung fibroblasts (MRC-5). Comparison of these values revealed therapeutic indices of 128–256 for antibacterial activity but a low selectivity index of 0.37 for anti-proliferative activity, indicating higher toxicity toward normal fibroblasts than cancer cells. Collectively, these findings suggest that QUB-2323 holds promise as a lead candidate for developing novel antibacterial and anticancer therapies, although its therapeutic applications may be limited by cytotoxicity.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis is embargoed until 31 December 2030.&lt;/i&gt;</dc:description>
          <dc:date>2026-10-01T16:19:52Z</dc:date>
          <dc:type>Text</dc:type>
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          <dc:identifier>10.17034/32641902.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2030-12-31</dc:rights>
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