Epitope Mapping of Anti-Bear Podoplanin Monoclonal Antibody PMab-247.


Journal

Monoclonal antibodies in immunodiagnosis and immunotherapy
ISSN: 2167-9436
Titre abrégé: Monoclon Antib Immunodiagn Immunother
Pays: United States
ID NLM: 101590955

Informations de publication

Date de publication:
Oct 2019
Historique:
pubmed: 20 9 2019
medline: 23 2 2020
entrez: 20 9 2019
Statut: ppublish

Résumé

Podoplanin (PDPN)/T1alpha is a type I transmembrane sialoglycoprotein, which is expressed on podocytes of the kidneys and type I alveolar cells of the lungs. PDPN is also known as Aggrus, a platelet aggregation-inducing factor, which comprises three platelet aggregation-stimulating (PLAG) domains (PLAG1, PLAG2, and PLAG3) in the N-terminus and PLAG-like domains (PLDs) in the middle of the PDPN protein. We have previously established a mouse anti-bear PDPN (bPDPN) monoclonal antibody (mAb) clone, PMab-247 using the Cell-Based Immunization and Screening (CBIS) method. PMab-247 is very useful in flow cytometry, Western blotting, and immunohistochemical (IHC) analyses; however, the binding epitope of PMab-247 has not been elucidated. In this study, we aimed to investigate the epitope of PMab-247 using enzyme-linked immunosorbent assay and IHC analyses. The results revealed that the critical epitopes of PMab-247 are Asp76, Arg78, Glu80, and Arg82 of bPDPN. The Glu80 and Arg82 are included in PLD of bPDPN. The findings of our study can be applied to the production of more functional anti-bPDPN mAbs.

Identifiants

pubmed: 31535919
doi: 10.1089/mab.2019.0025
doi:

Substances chimiques

Antibodies, Monoclonal 0
Epitopes 0
Membrane Glycoproteins 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

230-233

Auteurs

Yukinari Kato (Y)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.
New Industry Creation Hatchery Center, Tohoku University, Miyagi, Japan.

Junko Takei (J)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.
Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Yoshikazu Furusawa (Y)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.
New Industry Creation Hatchery Center, Tohoku University, Miyagi, Japan.

Yusuke Sayama (Y)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.

Masato Sano (M)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.

Satoru Konnai (S)

Laboratory of Infectious Diseases, Department of Disease Control, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan.
Department of Advanced Pharmaceutics, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan.

Atsushi Kobayashi (A)

Laboratory of Comparative Pathology, Faculty of Veterinary Medicine, Hokkaido University, Hokkaido, Japan.

Hiroyuki Harada (H)

Department of Oral and Maxillofacial Surgery, Graduate School of Medical and Dental Sciences, Tokyo Medical and Dental University, Tokyo, Japan.

Maki Takahashi (M)

Department of Pathology and Laboratory Medicine, Sendai Medical Center, Miyagi, Japan.

Hiroyoshi Suzuki (H)

Department of Pathology and Laboratory Medicine, Sendai Medical Center, Miyagi, Japan.

Shinji Yamada (S)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.

Mika K Kaneko (MK)

Department of Antibody Drug Development, Tohoku University Graduate School of Medicine, Miyagi, Japan.

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Classifications MeSH