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        <datestamp>2026-10-01T16:46:51Z</datestamp>
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          <dc:title>Identification and activity assessment of a bioactive peptide, QUB-2013, from the skin secretion of the Broad-folded Frog, (Phyllomedusa hypochondrialis)</dc:title>
          <dc:creator>Haoyu Gan (24168018)</dc:creator>
          <dc:subject>PUREID: 526185828</dc:subject>
          <dc:subject>Phylloseptin</dc:subject>
          <dc:subject>Antimicrobial peptides</dc:subject>
          <dc:subject>frog skin secretions</dc:subject>
          <dc:subject>molecular cloning</dc:subject>
          <dc:subject>antiproliferative effects</dc:subject>
          <dc:description>A complex array of antimicrobial peptides, neuroactive peptides, peptidase inhibitors, etc, representing a collection of physiologically- and structurally-interacting components, are found in frog skin secretions. Phylloseptins are a class of peptides produced from frog skin with an active structural sequence that displays antmicrobial efficacy in vitro against the E.coli, S.aureus and C.albicans.&lt;br&gt;&lt;br&gt;In the current study, a peptide (FLSLIPTAINAVSALAKHF-NH2), named QUB-2013, was discovered in Phyllomedusa hypochondrialis skin secretion by use of molecular cloning, and the crude peptide was subsequently obtained by solid phase synthesis and purified by reverse phase HPLC. MALDI-TOF MS was used to confirm the molecular mass, and a number of bioassays were performed on QUB-2013. As a result, QUB- 2013 was found to have anticancer cell activity and no appreciable cytotoxicity to horse red blood cells at concentrations less than 512 µM. Meanwhile, QUB- 2013 displayed antibacterial activity against Candida albicans below 256 µM and against E. coli and S. aureus below 128 µM. Furthermore, QUB-2013, in an MTT assay, was active at a concentration of 200 µM against NCI-H838 cancer .&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis is embargoed until 31 December 2028.&lt;/i&gt;</dc:description>
          <dc:date>2026-10-01T16:46:51Z</dc:date>
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          <dc:identifier>10.17034/32638209.v1</dc:identifier>
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          <dc:rights>All Rights Reserved</dc:rights>
          <dc:rights>Open Access after 2028-12-31</dc:rights>
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