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Article: Development of a phage display panning strategy utilizing crude antigens: isolation of MERS-CoV nucleoprotein human antibodies

TitleDevelopment of a phage display panning strategy utilizing crude antigens: isolation of MERS-CoV nucleoprotein human antibodies
Authors
Issue Date2019
PublisherNature Research (part of Springer Nature): Fully open access journals. The Journal's web site is located at http://www.nature.com/srep/index.html
Citation
Scientific Reports, 2019, v. 9 n. 1, p. article no. 6088 How to Cite?
AbstractAntibody phage display has been pivotal in the quest to generate human monoclonal antibodies for biomedical and research applications. Target antigen preparation is a main bottleneck associated with the panning process. This includes production complexity, downstream purification, quality and yield. In many instances, purified antigens are preferred for panning but this may not be possible for certain difficult target antigens. Here, we describe an improved procedure of affinity selection against crude or non-purified antigen by saturation of non-binders with blocking agents to promote positive binder enrichment termed as Yin-Yang panning. A naïve human scFv library with kappa light chain repertoire with a library size of 10 9 was developed. The improved Yin-Yang biopanning process was able to enrich monoclonal antibodies specific to the MERS-CoV nucleoprotein. Three unique monoclonal antibodies were isolated in the process. The Yin-Yang biopanning method highlights the possibility of utilizing crude antigens for the isolation of monoclonal antibodies by phage display. © 2019, The Author(s).
Persistent Identifierhttp://hdl.handle.net/10722/276338
ISSN
2021 Impact Factor: 4.996
2020 SCImago Journal Rankings: 1.240
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorLim, CC-
dc.contributor.authorWoo, PCY-
dc.contributor.authorLim, TS-
dc.date.accessioned2019-09-10T03:01:05Z-
dc.date.available2019-09-10T03:01:05Z-
dc.date.issued2019-
dc.identifier.citationScientific Reports, 2019, v. 9 n. 1, p. article no. 6088-
dc.identifier.issn2045-2322-
dc.identifier.urihttp://hdl.handle.net/10722/276338-
dc.description.abstractAntibody phage display has been pivotal in the quest to generate human monoclonal antibodies for biomedical and research applications. Target antigen preparation is a main bottleneck associated with the panning process. This includes production complexity, downstream purification, quality and yield. In many instances, purified antigens are preferred for panning but this may not be possible for certain difficult target antigens. Here, we describe an improved procedure of affinity selection against crude or non-purified antigen by saturation of non-binders with blocking agents to promote positive binder enrichment termed as Yin-Yang panning. A naïve human scFv library with kappa light chain repertoire with a library size of 10 9 was developed. The improved Yin-Yang biopanning process was able to enrich monoclonal antibodies specific to the MERS-CoV nucleoprotein. Three unique monoclonal antibodies were isolated in the process. The Yin-Yang biopanning method highlights the possibility of utilizing crude antigens for the isolation of monoclonal antibodies by phage display. © 2019, The Author(s).-
dc.languageeng-
dc.publisherNature Research (part of Springer Nature): Fully open access journals. The Journal's web site is located at http://www.nature.com/srep/index.html-
dc.relation.ispartofScientific Reports-
dc.titleDevelopment of a phage display panning strategy utilizing crude antigens: isolation of MERS-CoV nucleoprotein human antibodies-
dc.typeArticle-
dc.identifier.emailWoo, PCY: pcywoo@hkucc.hku.hk-
dc.identifier.authorityWoo, PCY=rp00430-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1038/s41598-019-42628-6-
dc.identifier.pmid30988390-
dc.identifier.scopuseid_2-s2.0-85064446357-
dc.identifier.hkuros304193-
dc.identifier.volume9-
dc.identifier.issue1-
dc.identifier.spagearticle no. 6088-
dc.identifier.epagearticle no. 6088-
dc.identifier.isiWOS:000464495800012-
dc.publisher.placeUnited Kingdom-
dc.identifier.issnl2045-2322-

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