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        <datestamp>2026-10-01T17:16:37Z</datestamp>
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          <dc:title>Discovery and bioactivity assessment of a novel peptide from the skin secretion of the Senegal running frog Kassina senegalens</dc:title>
          <dc:creator>Chunyuan Zhou (7543340)</dc:creator>
          <dc:subject>PUREID: 250506595</dc:subject>
          <dc:subject>Antimicrobial peptide</dc:subject>
          <dc:subject>bioactivity assessment</dc:subject>
          <dc:subject>broad-spectrum antimicrobial activity</dc:subject>
          <dc:subject>low haemolysis activity</dc:subject>
          <dc:subject>novel peptide</dc:subject>
          <dc:description>Frog skin is characterised with an abundance of biologically active antimicrobial peptides (AMPs) with a broad-spectrum effect against a variety of microorganisms. The contribution of their complex and diverse structures, physicochemical properties and mechanisms of biological activity, have been discovered and widely reported. In this study, a novel peptide named QUB-1923 was identified from the skin secretion of the Senegal running frog, Kassina senegalensis. The sequence of the mature peptide (FYHLSALIHGIKQRLK) was deduced from the cloned cDNA encoding a prepropeptide. Subsequently, this peptide was chemically synthesised by solid-phase synthesis. Following on from the purification by RP-HPLC and MALDI-TOF MS, the antimicrobial, anti-cancer cell proliferative and haemolytic activities of the purified peptide QUB-1923 were investigated. Results from antimicrobial assays have shown that this peptide has a broad-spectrum antimicrobial effect on S. aureus, E. coli and C. albicans. Notably, this peptide displayed the highest antimicrobial activity against E. coli (MIC=4 μM, and MBC=8 μM). On the other hand, this peptide only caused approximately 20% growth inhibition on lung cancer cell line H838 at a concentration of 100 μM. Additionally, this peptide demonstrated less than 10% haemolysis at a concentration of 256µM. These results suggest that this novel peptide is worthy of attention as a new antibacterial lead due to its potent inhibitory and bactericidal effects against Gram-ve bacteria, along with a low level of haemolysis.&lt;br&gt;&lt;i&gt;&lt;br&gt;Thesis embargoed until 31 December 2026&lt;/i&gt;.</dc:description>
          <dc:date>2026-10-01T17:16:37Z</dc:date>
          <dc:type>Text</dc:type>
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          <dc:identifier>10.17034/32631807.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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