Engineering a Novel Antibody-peptide Bispecific Fusion Protein Against MERS-CoV
aut.relation.articlenumber | 53 | en_NZ |
aut.relation.issue | 4 | en_NZ |
aut.relation.journal | Antibodies | en_NZ |
aut.relation.volume | 8 | en_NZ |
aut.researcher | Drabsch, Julie | |
dc.contributor.author | Wang, L | en_NZ |
dc.contributor.author | Xu, J | en_NZ |
dc.contributor.author | Kong, Y | en_NZ |
dc.contributor.author | Liang, R | en_NZ |
dc.contributor.author | Li, W | en_NZ |
dc.contributor.author | Li, J | en_NZ |
dc.contributor.author | Lu, J | en_NZ |
dc.contributor.author | Dimitrov, DS | en_NZ |
dc.contributor.author | Yu, F | en_NZ |
dc.contributor.author | Wu, Y | en_NZ |
dc.contributor.author | Ying, T | en_NZ |
dc.date.accessioned | 2020-06-28T23:46:31Z | |
dc.date.available | 2020-06-28T23:46:31Z | |
dc.date.copyright | 2019 | en_NZ |
dc.date.issued | 2019 | en_NZ |
dc.description.abstract | In recent years, tremendous efforts have been made in the engineering of bispecific or multi-specific antibody-based therapeutics by combining two or more functional antigen-recognizing elements into a single construct. However, to the best of our knowledge there has been no reported cases of effective antiviral antibody-peptide bispecific fusion proteins. We previously developed potent fully human monoclonal antibodies and inhibitory peptides against Middle East Respiratory Syndrome Coronavirus (MERS-CoV), a novel coronavirus that causes severe acute respiratory illness with high mortality. Here, we describe the generation of antibody-peptide bispecific fusion proteins, each of which contains an anti-MERS-CoV single-chain antibody m336 (or normal human IgG1 CH3 domain as a control) linked with, or without, a MERS-CoV fusion inhibitory peptide HR2P. We found that one of these fusion proteins, designated as m336 diabody-pep, exhibited more potent inhibitory activity than the antibody or the peptide alone against pseudotyped MERS-CoV infection and MERS-CoV S protein-mediated cell-cell fusion, suggesting its potential to be developed as an effective bispecific immunotherapeutic for clinical use. | en_NZ |
dc.identifier.citation | Antibodies 2019, 8(4), 53; https://doi.org/10.3390/antib8040053 | |
dc.identifier.doi | 10.3390/antib8040053 | en_NZ |
dc.identifier.issn | 2073-4468 | en_NZ |
dc.identifier.uri | https://hdl.handle.net/10292/13463 | |
dc.language | eng | en_NZ |
dc.publisher | MDPI AG | en_NZ |
dc.relation.uri | https://www.mdpi.com/2073-4468/8/4/53 | |
dc.rights | This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. | |
dc.rights.accessrights | OpenAccess | en_NZ |
dc.subject | MERS-CoV | en_NZ |
dc.subject | Bispecific | en_NZ |
dc.subject | Immunotherapeutics | en_NZ |
dc.subject | mAbs | en_NZ |
dc.subject | Polypeptides | en_NZ |
dc.title | Engineering a Novel Antibody-peptide Bispecific Fusion Protein Against MERS-CoV | en_NZ |
dc.type | Journal Article | |
pubs.elements-id | 365752 | |
pubs.organisational-data | /AUT | |
pubs.organisational-data | /AUT/Health & Environmental Science | |
pubs.organisational-data | /AUT/Health & Environmental Science/Interprofessional Health | |
pubs.organisational-data | /AUT/PBRF | |
pubs.organisational-data | /AUT/PBRF/PBRF Health and Environmental Sciences | |
pubs.organisational-data | /AUT/PBRF/PBRF Health and Environmental Sciences/HI Interprofessional 2018 PBRF |
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