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        <identifier>oai:figshare.com:article/32640075</identifier>
        <datestamp>2026-10-01T16:34:29Z</datestamp>
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          <dc:title>Identification and bioactivity evaluation of a novel temporin peptide, QUB-1347, from the skin secretion of Rana dybowskii</dc:title>
          <dc:creator>Xinyuan Dong (302683)</dc:creator>
          <dc:subject>PUREID: 612473280</dc:subject>
          <dc:subject>Antimicrobial peptides (AMPs)</dc:subject>
          <dc:subject>QUB-1347</dc:subject>
          <dc:subject>Rana dybowskii</dc:subject>
          <dc:subject>biological activity</dc:subject>
          <dc:subject>antibiotic resistance</dc:subject>
          <dc:description>At present, many pathogenic microorganisms have developed serious resistance, so scientists are working to find a new type of treatment drugs to replace traditional antibiotics. Antimicrobial peptides (AMPs) have a broad spectrum of antibacterial activity and have attracted great interest from scientists because of their potential biological activities against bacteria, fungi, viruses and cancer cells. &lt;br&gt;&lt;br&gt;In this study, shotgun cloning was utilized to isolate and identify a cDNA encoding an AMP precursor from the skin secretion of Rana dybowskii. The mature peptide that was obtained, FIGPIISALASLF-NH2, has 14 amino acid residues. Based on its molecular mass, this peptide was given the name QUB-1347. After sufficient peptides were obtained via SPPS, QUB-1347 was subjected to a number of tests to ascertain its biological activity. &lt;br&gt;&lt;br&gt;In the antimicrobial assay, QUB-1347 showed significant antimicrobial activity only against Gram-positive bacteria, but not against Gram-negative bacteria and yeast. Staphylococcus aureus (Gram-positive bacterium), Escherichia coli (Gram-negative bacterium) and Candida albicans (yeast), had MICs of 16, &gt;128 and &gt;128 µM respectively. Meanwhile, QUB-1347 showed low cytotoxicity to equine red cells, it demonstrated haemolysis of less than 20% at 64 µM. Moreover, QUB-1347 had antiproliferative activity on H838 cancer cells, and the effect was significantly enhanced when the concentration was higher than 25 µM, and the IC50 was 18.65 µM.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis is embargoed until 31 December 2029&lt;/i&gt;.&lt;br&gt;</dc:description>
          <dc:date>2026-10-01T16:34:29Z</dc:date>
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          <dc:identifier>10.17034/32640075.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2029-12-31</dc:rights>
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