{"id":{"repo_id":"qu-belfast","oai_identifier":"oai:pure.qub.ac.uk/portal:studenttheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f"},"canonical_url":"https://search.dev.ndltd.org/etd/qu-belfast/oai:pure.qub.ac.uk/portal:studenttheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f","repository":{"repo_id":"qu-belfast","name":"Queen's University Belfast","base_url":"https://pureadmin.qub.ac.uk/ws/oai"},"display":{"title":"Identification and functional assessment of a bioactive peptide QUB-2984 from the skin secretion of the red-eyed tree frog, Agalychnis callidryas","abstract":"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. <br/><i><br/>Thesis embargoed until 31 December 2026</i>.","abstract_html":"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;.","abstract_has_math":false,"creators":["Tang, Ziyan"],"institution":"Queen's University Belfast","degree_name":"Master of Philosophy","degree_level":"Masters Thesis","degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Zhou, Mei","Wang, Lei","Chen, Tianbao"],"committee_chairs":[],"committee_members":[],"year":2021,"date_issued":"2021-12","date_published":"2021-12","updated_at":"2026-07-24T03:56:04Z","subjects":["Antimicrobial peptides (AMPs)","molecular cloning","antimicrobial activity","haemolytic activity","MTT antiproliferation assay"],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[{"key":"dc:identifier","label":"Identifier","values":["oai:pure.qub.ac.uk/portal:studenttheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f"],"render_values":[{"text":"oai:pure.qub.ac.uk/portal:studenttheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f","href":null,"code":true}]}]},"links":{"outbound_url":"https://pure.qub.ac.uk/en/studentTheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f","outbound_label":"Repository record","outbound_source":"dc:identifier"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Zhou, Mei","Wang, Lei","Chen, Tianbao"]},{"key":"dc:contributor.sponsor","label":"Sponsor","values":["Queen's University & China Scholarship Council"]},{"key":"dc:creator","label":"Author","values":["Tang, Ziyan"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date","label":"Dc Date","values":["2021-12"]},{"key":"dc:date.issued","label":"Date","values":["2021-12"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["School of Pharmacy"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["Queen's University Belfast"]},{"key":"dc:relation.isreferencedby","label":"Dc Relation Isreferencedby","values":["https://pure.qub.ac.uk/en/studentTheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f"]},{"key":"dc:type","label":"Dc Type","values":["Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Masters Thesis"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["Master of Philosophy"]}]},{"id":"subjects_keywords","label":"Subjects and Keywords","entries":[{"key":"dc:subject","label":"Dc Subject","values":["Antimicrobial peptides (AMPs)","molecular cloning","antimicrobial activity","haemolytic activity","MTT antiproliferation assay"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language","label":"Dc Language","values":["eng"]},{"key":"dc:rights.embargodate","label":"Dc Rights Embargodate","values":["2026-12-31"]},{"key":"dc:rights.embargoreason","label":"Dc Rights Embargoreason","values":["/dk/atira/pure/core/document/studentthesisembargoreason/publicationissues"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier","label":"Identifier","values":["oai:pure.qub.ac.uk/portal:studenttheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f","https://pure.qub.ac.uk/en/studentTheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["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. <br/><i><br/>Thesis embargoed until 31 December 2026</i>."]},{"key":"dc:title","label":"Title","values":["Identification and functional assessment of a bioactive peptide QUB-2984 from the skin secretion of the red-eyed tree frog, Agalychnis callidryas"]}]}],"canonical_facts":{"dc:contributor.advisor":["Zhou, Mei","Wang, Lei","Chen, Tianbao"],"dc:contributor.sponsor":["Queen's University & China Scholarship Council"],"dc:creator":["Tang, Ziyan"],"dc:date":["2021-12"],"dc:date.issued":["2021-12"],"dc:description.abstract":["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. <br/><i><br/>Thesis embargoed until 31 December 2026</i>."],"dc:identifier":["oai:pure.qub.ac.uk/portal:studenttheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f","https://pure.qub.ac.uk/en/studentTheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f"],"dc:language":["eng"],"dc:publisher.department":["School of Pharmacy"],"dc:publisher.institution":["Queen's University Belfast"],"dc:relation.isreferencedby":["https://pure.qub.ac.uk/en/studentTheses/ad928ab9-d132-43e9-b5bd-d5c35c3e081f"],"dc:rights.embargodate":["2026-12-31"],"dc:rights.embargoreason":["/dk/atira/pure/core/document/studentthesisembargoreason/publicationissues"],"dc:subject":["Antimicrobial peptides (AMPs)","molecular cloning","antimicrobial activity","haemolytic activity","MTT antiproliferation assay"],"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:type":["Thesis"],"dc:type.qualificationlevel":["Masters Thesis"],"dc:type.qualificationname":["Master of Philosophy"]},"updated_at":"2026-07-24T03:56:04Z"}