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        <identifier>oai:figshare.com:article/32633370</identifier>
        <datestamp>2026-10-01T17:03:51Z</datestamp>
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          <dc:title>Identification and bioactivity assessment of a host-defence peptide, QUB-2654, from the skin secretion of the frog, Agalychnis callidryas</dc:title>
          <dc:creator>Ruiling Chen (24165612)</dc:creator>
          <dc:subject>PUREID: 366309743</dc:subject>
          <dc:subject>Antimicrobial peptides</dc:subject>
          <dc:subject>Agalychnis callidryas</dc:subject>
          <dc:subject>antibacterial</dc:subject>
          <dc:subject>anti-lung cancer</dc:subject>
          <dc:subject>haemolytic activity</dc:subject>
          <dc:description>Amphibian skin secretions contain a wide array of antimicrobial peptides with biological activities, providing an effective first-line of defence against microbial invasion. This thesis aims to characterise an antimicrobial peptide from the skin secretion of the Central American red-eyed tree frog, Agalychnis callidryas and to study its biological properties. Firstly, the cDNA sequence encoding an antimicrobial peptide (QUB-2654) precursor, was identified from the frog skin secretions extracted mRNAs through rapid-amplification of cDNA ends (RACE) PCR, molecular cloning and Sanger sequencing strategies. Next, the peptide was synthesised using a solid-phase peptide synthesiser, purified by reversed-phase high-performance liquid chromatography and corroborated by MALDI-TOF mass spectrometry. The purified peptide was tested for its antimicrobial activity, anti-lung cancer cell activity and haemolytic effect, by a series of bioassays. This study showed that QUB-2654 had significant bacteriostatic and bactericidal activities against a Gram-positive bacterium, Staphylococcus aureus (ATCC-CRM 6538) (MIC=3.125 µM, MBC=6.25 µM) and a Gram-negative bacterium, Escherichia coli (ATCC-CRM 8739) (MIC/MBC=6.25 µM), but the MIC value against Candida albicans (ATCC-CRM 10231) was not detected even at the highest peptide concentration. In addition, QUB-2654 statistically demonstrated anti-proliferative and killing effects against NCI-H838 human lung cancer cells at and above a concentration of 10 µM. The peptide concentration required to achieve half-maximal inhibition (IC50) of the NCI-H838 cells was 11.32 µM. This peptide was not haemolytic (&lt;5% haemolysis) at the MBC values for S.aureus and E.coli, and at the IC50 value for NCI-H838 cells. These results suggest that peptide QUB-2654 has the potential to be developed as an antibacterial and anticancer drug.&lt;br&gt;&lt;br&gt;&lt;i&gt;Thesis is embargoed until 31 December 2027.&lt;/i&gt;</dc:description>
          <dc:date>2026-10-01T17:03:51Z</dc:date>
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          <dc:identifier>10.17034/32633370.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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