Cargando…
G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity
The recognition specificity of monoclonal antibodies (mAbs) has made mAbs among the most frequently used tools in both basic science research and in clinical diagnosis and therapies. Precise determination of the epitope allows the development of epitope tag systems to be used with recombinant protei...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339894/ https://www.ncbi.nlm.nih.gov/pubmed/28266535 http://dx.doi.org/10.1038/srep43480 |
_version_ | 1782512739472637952 |
---|---|
author | Tatsumi, Kasumi Sakashita, Gyosuke Nariai, Yuko Okazaki, Kosuke Kato, Hiroaki Obayashi, Eiji Yoshida, Hisashi Sugiyama, Kanako Park, Sam-Yong Sekine, Joji Urano, Takeshi |
author_facet | Tatsumi, Kasumi Sakashita, Gyosuke Nariai, Yuko Okazaki, Kosuke Kato, Hiroaki Obayashi, Eiji Yoshida, Hisashi Sugiyama, Kanako Park, Sam-Yong Sekine, Joji Urano, Takeshi |
author_sort | Tatsumi, Kasumi |
collection | PubMed |
description | The recognition specificity of monoclonal antibodies (mAbs) has made mAbs among the most frequently used tools in both basic science research and in clinical diagnosis and therapies. Precise determination of the epitope allows the development of epitope tag systems to be used with recombinant proteins for various purposes. Here we describe a new family of tag derived from the epitope recognized by a highly specific mAb G196. The minimal epitope was identified as the five amino acid sequence Asp-Leu-Val-Pro-Arg. Permutation analysis was used to characterize the binding requirements of mAb G196, and the variable regions of the mAb G196 were identified and structurally analyzed by X-ray crystallography. Isothermal titration calorimetry revealed the high affinity (K(d) = 1.25 nM) of the mAb G196/G196-epitope peptide interaction, and G196-tag was used to detect several recombinant cytosolic and nuclear proteins in human and yeast cells. mAb G196 is valuable for developing a new peptide tagging system for cell biology and biochemistry research. |
format | Online Article Text |
id | pubmed-5339894 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-53398942017-03-10 G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity Tatsumi, Kasumi Sakashita, Gyosuke Nariai, Yuko Okazaki, Kosuke Kato, Hiroaki Obayashi, Eiji Yoshida, Hisashi Sugiyama, Kanako Park, Sam-Yong Sekine, Joji Urano, Takeshi Sci Rep Article The recognition specificity of monoclonal antibodies (mAbs) has made mAbs among the most frequently used tools in both basic science research and in clinical diagnosis and therapies. Precise determination of the epitope allows the development of epitope tag systems to be used with recombinant proteins for various purposes. Here we describe a new family of tag derived from the epitope recognized by a highly specific mAb G196. The minimal epitope was identified as the five amino acid sequence Asp-Leu-Val-Pro-Arg. Permutation analysis was used to characterize the binding requirements of mAb G196, and the variable regions of the mAb G196 were identified and structurally analyzed by X-ray crystallography. Isothermal titration calorimetry revealed the high affinity (K(d) = 1.25 nM) of the mAb G196/G196-epitope peptide interaction, and G196-tag was used to detect several recombinant cytosolic and nuclear proteins in human and yeast cells. mAb G196 is valuable for developing a new peptide tagging system for cell biology and biochemistry research. Nature Publishing Group 2017-03-07 /pmc/articles/PMC5339894/ /pubmed/28266535 http://dx.doi.org/10.1038/srep43480 Text en Copyright © 2017, The Author(s) http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Tatsumi, Kasumi Sakashita, Gyosuke Nariai, Yuko Okazaki, Kosuke Kato, Hiroaki Obayashi, Eiji Yoshida, Hisashi Sugiyama, Kanako Park, Sam-Yong Sekine, Joji Urano, Takeshi G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity |
title | G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity |
title_full | G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity |
title_fullStr | G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity |
title_full_unstemmed | G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity |
title_short | G196 epitope tag system: a novel monoclonal antibody, G196, recognizes the small, soluble peptide DLVPR with high affinity |
title_sort | g196 epitope tag system: a novel monoclonal antibody, g196, recognizes the small, soluble peptide dlvpr with high affinity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5339894/ https://www.ncbi.nlm.nih.gov/pubmed/28266535 http://dx.doi.org/10.1038/srep43480 |
work_keys_str_mv | AT tatsumikasumi g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT sakashitagyosuke g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT nariaiyuko g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT okazakikosuke g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT katohiroaki g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT obayashieiji g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT yoshidahisashi g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT sugiyamakanako g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT parksamyong g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT sekinejoji g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity AT uranotakeshi g196epitopetagsystemanovelmonoclonalantibodyg196recognizesthesmallsolublepeptidedlvprwithhighaffinity |