Cargando…
Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor.
A mouse monoclonal antibody (IgG2b), 3C10, was produced against the truncated epidermal growth factor receptor (EGFR), encoded by the (type III) in-frame deletion mutation of 801 nucleotides of EGFR affecting the external domain, known to be expressed in some human glioblastoma. As this mutation new...
Autores principales: | , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
1996
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074493/ https://www.ncbi.nlm.nih.gov/pubmed/8645581 |
_version_ | 1782137978676576256 |
---|---|
author | Okamoto, S. Yoshikawa, K. Obata, Y. Shibuya, M. Aoki, S. Yoshida, J. Takahashi, T. |
author_facet | Okamoto, S. Yoshikawa, K. Obata, Y. Shibuya, M. Aoki, S. Yoshida, J. Takahashi, T. |
author_sort | Okamoto, S. |
collection | PubMed |
description | A mouse monoclonal antibody (IgG2b), 3C10, was produced against the truncated epidermal growth factor receptor (EGFR), encoded by the (type III) in-frame deletion mutation of 801 nucleotides of EGFR affecting the external domain, known to be expressed in some human glioblastoma. As this mutation newly generates a glycine residue at the fusion point, a 14 amino acid peptide around the fusion junction including this glycine was chemically synthesised and used for immunisation of (B6 x DBA/2) F1 mice. Flow cytometric analysis showed 3C10 antibody staining of a mouse NIH/3T3 transfectant (ERM5) with the type III EGFR deletion-mutant gene, but not one with wild-type EGFR. The antibody immunoprecipitated the truncated EGFR protein with a molecular mass of approximately 140 kDa from ERM5 cells. Immunostaining of glioblastomas revealed binding in the case with the type III EGFR mutation, the five other specimens without the mutation being negative despite overexpression of EGFR in some cases. IMAGES: |
format | Text |
id | pubmed-2074493 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 1996 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-20744932009-09-10 Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. Okamoto, S. Yoshikawa, K. Obata, Y. Shibuya, M. Aoki, S. Yoshida, J. Takahashi, T. Br J Cancer Research Article A mouse monoclonal antibody (IgG2b), 3C10, was produced against the truncated epidermal growth factor receptor (EGFR), encoded by the (type III) in-frame deletion mutation of 801 nucleotides of EGFR affecting the external domain, known to be expressed in some human glioblastoma. As this mutation newly generates a glycine residue at the fusion point, a 14 amino acid peptide around the fusion junction including this glycine was chemically synthesised and used for immunisation of (B6 x DBA/2) F1 mice. Flow cytometric analysis showed 3C10 antibody staining of a mouse NIH/3T3 transfectant (ERM5) with the type III EGFR deletion-mutant gene, but not one with wild-type EGFR. The antibody immunoprecipitated the truncated EGFR protein with a molecular mass of approximately 140 kDa from ERM5 cells. Immunostaining of glioblastomas revealed binding in the case with the type III EGFR mutation, the five other specimens without the mutation being negative despite overexpression of EGFR in some cases. IMAGES: Nature Publishing Group 1996-06 /pmc/articles/PMC2074493/ /pubmed/8645581 Text en https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Article Okamoto, S. Yoshikawa, K. Obata, Y. Shibuya, M. Aoki, S. Yoshida, J. Takahashi, T. Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
title | Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
title_full | Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
title_fullStr | Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
title_full_unstemmed | Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
title_short | Monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
title_sort | monoclonal antibody against the fusion junction of a deletion-mutant epidermal growth factor receptor. |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2074493/ https://www.ncbi.nlm.nih.gov/pubmed/8645581 |
work_keys_str_mv | AT okamotos monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor AT yoshikawak monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor AT obatay monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor AT shibuyam monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor AT aokis monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor AT yoshidaj monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor AT takahashit monoclonalantibodyagainstthefusionjunctionofadeletionmutantepidermalgrowthfactorreceptor |