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        <datestamp>2026-10-01T17:04:06Z</datestamp>
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          <dc:title>The discovery, identification, and bioactivity screening of peptide, QUB-2335, from skin secretion of the frog, Amolops hainanensis</dc:title>
          <dc:creator>Wenjia Zhao (4898182)</dc:creator>
          <dc:subject>PUREID: 365374188</dc:subject>
          <dc:subject>Antimicrobial peptides (AMPs)</dc:subject>
          <dc:subject>antibiotic resistance</dc:subject>
          <dc:subject>Hainanenin</dc:subject>
          <dc:subject>amphibian skin secretion</dc:subject>
          <dc:subject>QUB-2335</dc:subject>
          <dc:description>Due to the resistance of antibiotics, the research of antimicrobial peptides has become a hot topic. In this study, a novel peptide named, QUB-2335, was identified and characterised from the skin secretion of the frog (Amolops hainanensis) by the strategy of ‘shotgun’ cloning. The deduced mature peptide sequence was confirmed as: FALGAVTKRLPSLFCLITRKC. QUB-2335 showed a broad-spectrum antimicrobial activity against Gram-positive bacteria, Gram-negative bacteria, and yeast. The result of QUB-2335 towards E. coli and S. aureus in MIC assays, were 4 μM and 4 μM, and in MBC assays, were 16 μM and 8 μM. Also, the MIC/MBC values of QUB-2335 against C. albicans, were is 64 μM and 128 μM. The haemolysis assay results showed that the QUB-2335 had only 27.1% haemolysis at the concentration of 256μM. The anticancer cell assay revealed a potent inhibition of cancer cell proliferation. At a concentration of 10-4 M, a significant impact of QUB-2335 was observed. These experiments on QUB-2335 revealed antibacterial and anticancer cell activities with potential of low side effects. Thus, this peptide has some value and potential to become a clinical drug after further research and modification.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis embargoed until 31st December 2027 &lt;/i&gt;</dc:description>
          <dc:date>2026-10-01T17:04:06Z</dc:date>
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          <dc:identifier>10.17034/32633343.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2027-12-31</dc:rights>
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