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        <datestamp>2026-10-01T17:16:22Z</datestamp>
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          <dc:title>Identification and functional assessment of a bioactive peptide QUB-2984 from the skin secretion of the red-eyed tree frog, Agalychnis callidryas</dc:title>
          <dc:creator>Ziyan Tang (12986718)</dc:creator>
          <dc:subject>PUREID: 250534325</dc:subject>
          <dc:subject>Antimicrobial peptides (AMPs)</dc:subject>
          <dc:subject>molecular cloning</dc:subject>
          <dc:subject>antimicrobial activity</dc:subject>
          <dc:subject>haemolytic activity</dc:subject>
          <dc:subject>MTT antiproliferation assay</dc:subject>
          <dc:description>Bioactive peptides secreted from amphibians have been studied broadly for their potency as alternative drugs to treat human diseases. This thesis is about a caerin-related peptide derived from red-eyed leaf frog, Agalychnis callidryas, which provided ideas for further antibiotic research. Herein, the objectives included the isolation, identification, and bioactivity assessment of this bioactive peptide named QUB-2984. Agalychnis callidryas skin secretions were collected by stimulating the frogs’ skin. The sequence of QUB-2984 (GMWGTVFKGIKTVAKHLLPHVFSSQQS) was obtained by ‘shotgun’ cloning through constructing a cDNA library with isolated mRNA, and tested by DNA Sanger sequencing. It was synthesised by solid phase peptide synthesis, purified by reversed-phase high-performance liquid chromatography and structurally-confirmed by MALDI-TOF MS. The MIC value against gram-positive bacteria S.aureus was 2μM, gram-negative bacteria E.coli was 2μM, and against the pathogenic yeast C. albicans was 8μM. QUB-2984 showed anticancer potency at the minimum concentration of 10-5M towards human cancer cells. In terms of haemolysis, it caused around 50% haemolytic effect at 64μM. Its haemolytic effect implied the possibility of side-effects towards mammalian cells, but its ability to exert both antibacterial and anticancer biological activity makes this study valuable as a pre-study foundation for designing new antibiotics against cancer or infectious diseases. &lt;br&gt;&lt;i&gt;&lt;br&gt;Thesis embargoed until 31 December 2026&lt;/i&gt;.</dc:description>
          <dc:date>2026-10-01T17:16:22Z</dc:date>
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          <dc:identifier>10.17034/32631837.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2026-12-31</dc:rights>
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