Cyclic peptides: Promising scaffolds for biopharmaceuticals

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dc.contributor.authorGang, Dong Hyeokko
dc.contributor.authorKim, Do Wookko
dc.contributor.authorPark, Hee-Sungko
dc.date.accessioned2018-12-20T08:03:36Z-
dc.date.available2018-12-20T08:03:36Z-
dc.date.created2018-12-14-
dc.date.created2018-12-14-
dc.date.issued2018-11-
dc.identifier.citationGENES, v.9, no.11-
dc.identifier.issn2073-4425-
dc.identifier.urihttp://hdl.handle.net/10203/248723-
dc.description.abstractTo date, small molecules and macromolecules, including antibodies, have been the most pursued substances in drug screening and development efforts. Despite numerous favorable features as a drug, these molecules still have limitations and are not complementary in many regards. Recently, peptide-based chemical structures that lie between these two categories in terms of both structural and functional properties have gained increasing attention as potential alternatives. In particular, peptides in a circular form provide a promising scaffold for the development of a novel drug class owing to their adjustable and expandable ability to bind a wide range of target molecules. In this review, we discuss recent progress in methodologies for peptide cyclization and screening and use of bioactive cyclic peptides in various applications. © 2018 by the authors. Licensee MDPI, Basel, Switzerland.-
dc.languageEnglish-
dc.publisherMDPI AG-
dc.titleCyclic peptides: Promising scaffolds for biopharmaceuticals-
dc.typeArticle-
dc.identifier.wosid000451636700042-
dc.identifier.scopusid2-s2.0-85057119987-
dc.type.rimsART-
dc.citation.volume9-
dc.citation.issue11-
dc.citation.publicationnameGENES-
dc.identifier.doi10.3390/genes9110557-
dc.contributor.localauthorPark, Hee-Sung-
dc.description.isOpenAccessN-
dc.type.journalArticleReview-
dc.subject.keywordAuthorcyclic peptides-
dc.subject.keywordAuthorbiopharmaceuticals-
dc.subject.keywordAuthormRNA display-
dc.subject.keywordAuthoryeast two hybrid-
dc.subject.keywordPlusMESSENGER-RNA DISPLAY-
dc.subject.keywordPlusIMPROVING TUMOR UPTAKE-
dc.subject.keywordPlusIN-VITRO SELECTION-
dc.subject.keywordPlusPROTEIN INTERACTIONS-
dc.subject.keywordPlusTHIOESTERASE DOMAIN-
dc.subject.keywordPlusRIBOSOMAL SYNTHESIS-
dc.subject.keywordPlusRATIONAL DESIGN-
dc.subject.keywordPlusPHAGE DISPLAY-
dc.subject.keywordPlusSPLIT INTEIN-
dc.subject.keywordPlusRGD PEPTIDE-
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