Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.

Here, we provide direct evidence that using recombinant proteins expressed in eukaryotic cells as antigen is a practical way to generate monoclonal antibodies (mAbs) against heavily glycosylated proteins. Heavily glycosylated proteins are typically difficult targets for mAb generation, being limited...

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Main Authors: Weikai Zhang, Zhitao Li, Zihua Wang, Chunyan Yue, Hui Zheng, Ren Li, Mingxing Zhou, Zhiyuan Hu, Zewen Wei, Qin Li
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2018-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5806877?pdf=render
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spelling doaj-ff3720f9baf64630b43886cdc0db6b5d2020-11-25T02:48:44ZengPublic Library of Science (PLoS)PLoS ONE1932-62032018-01-01132e019250610.1371/journal.pone.0192506Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.Weikai ZhangZhitao LiZihua WangChunyan YueHui ZhengRen LiMingxing ZhouZhiyuan HuZewen WeiQin LiHere, we provide direct evidence that using recombinant proteins expressed in eukaryotic cells as antigen is a practical way to generate monoclonal antibodies (mAbs) against heavily glycosylated proteins. Heavily glycosylated proteins are typically difficult targets for mAb generation, being limited by unsatisfactory affinity and low specificity. Using the heavily glycosylated CD45 protein as an example, we demonstrate the entire process of expressing the protein in eukaryotic cells and using it as an antigen to generate CD45-targeting mAbs in mice. The mAbs generated showed robust affinity and specificity, which are crucial factors for differentiate circulating tumor cells from white blood cells in human breast cancer patient samples. Only 1 cell fusion and 2 cyclic sub-cloning steps were necessary before mAbs with satisfactory performance were obtained.http://europepmc.org/articles/PMC5806877?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Weikai Zhang
Zhitao Li
Zihua Wang
Chunyan Yue
Hui Zheng
Ren Li
Mingxing Zhou
Zhiyuan Hu
Zewen Wei
Qin Li
spellingShingle Weikai Zhang
Zhitao Li
Zihua Wang
Chunyan Yue
Hui Zheng
Ren Li
Mingxing Zhou
Zhiyuan Hu
Zewen Wei
Qin Li
Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.
PLoS ONE
author_facet Weikai Zhang
Zhitao Li
Zihua Wang
Chunyan Yue
Hui Zheng
Ren Li
Mingxing Zhou
Zhiyuan Hu
Zewen Wei
Qin Li
author_sort Weikai Zhang
title Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.
title_short Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.
title_full Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.
title_fullStr Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.
title_full_unstemmed Generation of a monoclonal antibody recognizing the heavily glycosylated CD45 protein and its application on identifying circulating tumor cells.
title_sort generation of a monoclonal antibody recognizing the heavily glycosylated cd45 protein and its application on identifying circulating tumor cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2018-01-01
description Here, we provide direct evidence that using recombinant proteins expressed in eukaryotic cells as antigen is a practical way to generate monoclonal antibodies (mAbs) against heavily glycosylated proteins. Heavily glycosylated proteins are typically difficult targets for mAb generation, being limited by unsatisfactory affinity and low specificity. Using the heavily glycosylated CD45 protein as an example, we demonstrate the entire process of expressing the protein in eukaryotic cells and using it as an antigen to generate CD45-targeting mAbs in mice. The mAbs generated showed robust affinity and specificity, which are crucial factors for differentiate circulating tumor cells from white blood cells in human breast cancer patient samples. Only 1 cell fusion and 2 cyclic sub-cloning steps were necessary before mAbs with satisfactory performance were obtained.
url http://europepmc.org/articles/PMC5806877?pdf=render
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