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Pathogen-derived peptides in drug targeting and its therapeutic approach

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dc.contributor.authorMun, Seok-Jun-
dc.contributor.authorCho, Euni-
dc.contributor.authorKim, Jae -Sung-
dc.contributor.authorYang, Chul-Su-
dc.date.accessioned2023-05-03T09:48:21Z-
dc.date.available2023-05-03T09:48:21Z-
dc.date.issued2022-10-
dc.identifier.issn0168-3659-
dc.identifier.issn1873-4995-
dc.identifier.urihttps://scholarworks.bwise.kr/erica/handle/2021.sw.erica/112785-
dc.description.abstractPeptides, short stretches of amino acids or small proteins that occupy a strategic position between proteins and amino acids, are readily accessible by chemical and biological methods. With ideal properties for forming high -affinity and specific interactions with host target proteins, they have established an important niche in the drug development spectrum complementing small molecule and biological therapeutics. Among the most successful biomedicines in use today, peptide-based drugs show great promise. This, coupled with recent advances in synthetic and nanochemical biology, has led to the creation of tailor-made peptide therapeutics for improved biocompatibility. This review presents an overview of the latest research on pathogen-derived, host-cell -inter-acting peptides. It also highlights strategies for using peptide-based therapeutics that address cellular transport challenges through the introduction of nanoparticles that serve as platforms to facilitate the delivery of peptide biologics and therapeutics for treating various inflammatory diseases. Finally, this paper describes future per-spectives, specific pathogen-based peptides that can enhance specificity, efficiency, and capacity in functional peptide-based therapeutics, which are in the spotlight as new treatment alternatives for various diseases, and also presents verified sequences and targets that can increase chemical and pharmacological value.-
dc.format.extent18-
dc.language영어-
dc.language.isoENG-
dc.publisherElsevier BV-
dc.titlePathogen-derived peptides in drug targeting and its therapeutic approach-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1016/j.jconrel.2022.08.041-
dc.identifier.scopusid2-s2.0-85137617760-
dc.identifier.wosid000853344900003-
dc.identifier.bibliographicCitationJournal of Controlled Release, v.350, pp 716 - 733-
dc.citation.titleJournal of Controlled Release-
dc.citation.volume350-
dc.citation.startPage716-
dc.citation.endPage733-
dc.type.docTypeReview-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaChemistry-
dc.relation.journalResearchAreaPharmacology & Pharmacy-
dc.relation.journalWebOfScienceCategoryChemistry, Multidisciplinary-
dc.relation.journalWebOfScienceCategoryPharmacology & Pharmacy-
dc.subject.keywordPlusFUNGAL IMMUNOMODULATORY PROTEIN-
dc.subject.keywordPlusD-AMINO-ACID-
dc.subject.keywordPlusHELICOBACTER-PYLORI-
dc.subject.keywordPlusVACCINIA VIRUS-
dc.subject.keywordPlusGANODERMA-TSUGAE-
dc.subject.keywordPlusPENETRATING PEPTIDE-
dc.subject.keywordPlusSTRUCTURAL MIMICRY-
dc.subject.keywordPlusCRYSTAL-STRUCTURE-
dc.subject.keywordPlusDELIVERY SYSTEMS-
dc.subject.keywordPlusORAL DELIVERY-
dc.subject.keywordAuthorMicrobe-
dc.subject.keywordAuthorProtein -protein interaction-
dc.subject.keywordAuthorPeptide-
dc.subject.keywordAuthorInflammatory disease-
dc.subject.keywordAuthorTherapeutics-
dc.identifier.urlhttps://www.sciencedirect.com/science/article/pii/S016836592200548X?via%3Dihub-
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