Amphipathic Alpha-Helical Peptides AH1 and AH3 Facilitate Immunogenicity of Enhanced Green Fluorescence Protein in Rainbow Trout (Oncorhynchus mykiss)

dc.contributor.authorPeng, Kuan Chieh
dc.contributor.authorWong, Ten-Tsao
dc.date.accessioned2025-08-28T16:10:49Z
dc.date.issued2025-08-04
dc.description.abstractVaccination is the most effective method to counteract infectious diseases in farmed fish. It secures aquaculture production and safeguards the wild stock and aquatic ecosystem from catastrophic contagious diseases. In vaccine development, recombinant subunit vaccines are favorable candidates since they can be economically produced in large quantities without growing many pathogens, as in inactivated or attenuated vaccine production. However, recombinant subunit vaccines are often weak or deficient in immunogenicity, resulting in inadequate defenses against infections. Technologies that can increase the immunogenicity of recombinant subunit vaccines are in desperate need. Enhanced green fluorescence protein (EGFP) has a low antigenicity and is susceptible to folding changes and losing fluorescence after fusing with other proteins. Using these valuable features of EGFP, we comprehend two amphipathic alpha-helical peptides, AH1 and AH3, derived from Hepatitis C virus and Influenza A virus, respectively, that can induce high immune responses of their fused EGFP in fish without affecting their folding. AH3-EGFP has the most elevated cell binding, significantly 62% and 36% higher than EGFP and AH1-EGFP, respectively. Immunizations with AH1-EGFP or AH3-EGFP significantly induced higher anti-EGFP antibody levels 300–500-fold higher than EGFP immunization after the boost injection in rainbow trout. Our results suggest that AH1 and AH3 effectively increase the immunogenicity of EGFP without influencing its structure. Further validation of their value in other recombinant proteins is necessary to demonstrate their broader utility in enhancing the immunogenicity of subunit vaccines. We also suggest that EGFP and its variants are promising candidates for initially screening proper immunogenicity-enhancing peptides or proteins to advance recombinant subunit vaccine development.
dc.description.sponsorshipThis research was funded by the University of Maryland, Baltimore County STRT7TEN1113 to T.-T.W.
dc.description.urihttps://www.mdpi.com/2077-1312/13/8/1497
dc.format.extent13 pages
dc.genrejournal articles
dc.identifierdoi:10.13016/m2zr7s-1tiz
dc.identifier.citationPeng, Kuan Chieh, and Ten-Tsao Wong. “Amphipathic Alpha-Helical Peptides AH1 and AH3 Facilitate Immunogenicity of Enhanced Green Fluorescence Protein in Rainbow Trout (Oncorhynchus Mykiss).” Journal of Marine Science and Engineering 13, no. 8 (2025): 1497. https://doi.org/10.3390/jmse13081497.
dc.identifier.urihttps://doi.org/10.3390/jmse13081497
dc.identifier.urihttp://hdl.handle.net/11603/40045
dc.language.isoen
dc.publisherMDPI
dc.relation.isAvailableAtThe University of Maryland, Baltimore County (UMBC)
dc.relation.ispartofUMBC Department of Marine Biotechnology
dc.relation.ispartofUMBC Faculty Collection
dc.rightsAttribution 4.0 International
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.subjectamphipathic alpha-helical peptides
dc.subjectgreen fluorescence protein
dc.subjectvaccine
dc.subjectaquaculture
dc.subjectimmunogenicity
dc.titleAmphipathic Alpha-Helical Peptides AH1 and AH3 Facilitate Immunogenicity of Enhanced Green Fluorescence Protein in Rainbow Trout (Oncorhynchus mykiss)
dc.typeText
dcterms.creatorhttps://orcid.org/0000-0001-5573-9767
dcterms.creatorhttps://orcid.org/0009-0003-2821-4457

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