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Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1

Diacylglycerol kinase δ (DGKδ) is a type II DGK, which catalyzes diacylglycerol phosphorylation to produce phosphatidic acid. DGKδ is expressed in several types of tissues and organs including the stomach, testis, bone marrow, and lymph node. Here, we established an anti-human DGKδ (hDGKδ) mAb, DdMa...

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Autores principales: Sano, Masato, Asano, Teizo, Kaneko, Mika K., Kato, Yukinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481522/
https://www.ncbi.nlm.nih.gov/pubmed/32944659
http://dx.doi.org/10.1016/j.bbrep.2020.100808
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author Sano, Masato
Asano, Teizo
Kaneko, Mika K.
Kato, Yukinari
author_facet Sano, Masato
Asano, Teizo
Kaneko, Mika K.
Kato, Yukinari
author_sort Sano, Masato
collection PubMed
description Diacylglycerol kinase δ (DGKδ) is a type II DGK, which catalyzes diacylglycerol phosphorylation to produce phosphatidic acid. DGKδ is expressed in several types of tissues and organs including the stomach, testis, bone marrow, and lymph node. Here, we established an anti-human DGKδ (hDGKδ) mAb, DdMab-1 (mouse IgG(2a), kappa), which is useful for Western blot analysis. We also introduced deletion or point mutations to hDGKδ, and performed western blotting to determine the binding epitope of DdMab-1. DdMab-1 reacted with the dN670 mutant, but not with the dN680 mutant, indicating that the N-terminus of the DdMab-1 epitope is mainly located between amino acids 670 and 680 of the protein. Further analysis using point mutants demonstrated that R675A, R678A, K679A, and K682A mutants were not detected, and V680A was only weakly detected by DdMab-1, indicating that Arg675, Arg678, Lys679, Val680 and Lys682 are important for binding of DdMab-1 to hDGKδ.
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spelling pubmed-74815222020-09-16 Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1 Sano, Masato Asano, Teizo Kaneko, Mika K. Kato, Yukinari Biochem Biophys Rep Research Article Diacylglycerol kinase δ (DGKδ) is a type II DGK, which catalyzes diacylglycerol phosphorylation to produce phosphatidic acid. DGKδ is expressed in several types of tissues and organs including the stomach, testis, bone marrow, and lymph node. Here, we established an anti-human DGKδ (hDGKδ) mAb, DdMab-1 (mouse IgG(2a), kappa), which is useful for Western blot analysis. We also introduced deletion or point mutations to hDGKδ, and performed western blotting to determine the binding epitope of DdMab-1. DdMab-1 reacted with the dN670 mutant, but not with the dN680 mutant, indicating that the N-terminus of the DdMab-1 epitope is mainly located between amino acids 670 and 680 of the protein. Further analysis using point mutants demonstrated that R675A, R678A, K679A, and K682A mutants were not detected, and V680A was only weakly detected by DdMab-1, indicating that Arg675, Arg678, Lys679, Val680 and Lys682 are important for binding of DdMab-1 to hDGKδ. Elsevier 2020-09-02 /pmc/articles/PMC7481522/ /pubmed/32944659 http://dx.doi.org/10.1016/j.bbrep.2020.100808 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by/4.0/ This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Article
Sano, Masato
Asano, Teizo
Kaneko, Mika K.
Kato, Yukinari
Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1
title Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1
title_full Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1
title_fullStr Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1
title_full_unstemmed Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1
title_short Epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody DdMab-1
title_sort epitope mapping of an anti-diacylglycerol kinase delta monoclonal antibody ddmab-1
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7481522/
https://www.ncbi.nlm.nih.gov/pubmed/32944659
http://dx.doi.org/10.1016/j.bbrep.2020.100808
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