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Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas

SC142-reactive antigen are highly glycosylated glycoproteins expressed on tissues of gastric and colon cancers but not on normal tissues. Murine SC142 antibody specific for the SC142-reactive antigen has been produced by immunisation with SNU16 stomach cancer cells. However, SC142 antibody has sever...

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Autores principales: Kim, D-J, Chung, J-H, Ryu, Y-S, Rhim, J-H, Kim, C-W, Suh, Y, Chung, H-K
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2002
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376138/
https://www.ncbi.nlm.nih.gov/pubmed/12177777
http://dx.doi.org/10.1038/sj.bjc.6600365
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author Kim, D-J
Chung, J-H
Ryu, Y-S
Rhim, J-H
Kim, C-W
Suh, Y
Chung, H-K
author_facet Kim, D-J
Chung, J-H
Ryu, Y-S
Rhim, J-H
Kim, C-W
Suh, Y
Chung, H-K
author_sort Kim, D-J
collection PubMed
description SC142-reactive antigen are highly glycosylated glycoproteins expressed on tissues of gastric and colon cancers but not on normal tissues. Murine SC142 antibody specific for the SC142-reactive antigen has been produced by immunisation with SNU16 stomach cancer cells. However, SC142 antibody has several potential problems such as high immunogenicity and poor tumour penetration owing to their large size. To improve tumour penetration potential in vivo, recombinant single-chain fragments have been produced using the original hybridoma cells as a source of variable heavy- and variable light-chain-encoding antibody genes. The use of the polymerase chain reaction, expression cloning technology and gene expression systems in E. coli has led to the production of SC142 single-chain fragments, which was similar in activity to the SC142 parent antibody confirmed by immunohistochemistry. Analysis by DNA sequencing, SDS–PAGE and Western blotting has demonstrated the integrity of the single-chain fragments. Competitive ELISA showed that SC142 single-chain fragments originated from parent SC142 antibody. BIAcore biosensor binding experiments showed that the SC142 single-chain fragments had an ideal dissociation rate constant as a tumour imaging reagent. These results illustrate the potential application of these novel products as an immunodiagnostic and further immunotherapeutic reagent. British Journal of Cancer (2002) 87, 405–413. doi:10.1038/sj.bjc.6600365 www.bjcancer.com © 2002 Cancer Research UK
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spelling pubmed-23761382009-09-10 Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas Kim, D-J Chung, J-H Ryu, Y-S Rhim, J-H Kim, C-W Suh, Y Chung, H-K Br J Cancer Molecular and Cellular Pathology SC142-reactive antigen are highly glycosylated glycoproteins expressed on tissues of gastric and colon cancers but not on normal tissues. Murine SC142 antibody specific for the SC142-reactive antigen has been produced by immunisation with SNU16 stomach cancer cells. However, SC142 antibody has several potential problems such as high immunogenicity and poor tumour penetration owing to their large size. To improve tumour penetration potential in vivo, recombinant single-chain fragments have been produced using the original hybridoma cells as a source of variable heavy- and variable light-chain-encoding antibody genes. The use of the polymerase chain reaction, expression cloning technology and gene expression systems in E. coli has led to the production of SC142 single-chain fragments, which was similar in activity to the SC142 parent antibody confirmed by immunohistochemistry. Analysis by DNA sequencing, SDS–PAGE and Western blotting has demonstrated the integrity of the single-chain fragments. Competitive ELISA showed that SC142 single-chain fragments originated from parent SC142 antibody. BIAcore biosensor binding experiments showed that the SC142 single-chain fragments had an ideal dissociation rate constant as a tumour imaging reagent. These results illustrate the potential application of these novel products as an immunodiagnostic and further immunotherapeutic reagent. British Journal of Cancer (2002) 87, 405–413. doi:10.1038/sj.bjc.6600365 www.bjcancer.com © 2002 Cancer Research UK Nature Publishing Group 2002-08-12 /pmc/articles/PMC2376138/ /pubmed/12177777 http://dx.doi.org/10.1038/sj.bjc.6600365 Text en Copyright © 2002 Cancer Research UK 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 Molecular and Cellular Pathology
Kim, D-J
Chung, J-H
Ryu, Y-S
Rhim, J-H
Kim, C-W
Suh, Y
Chung, H-K
Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas
title Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas
title_full Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas
title_fullStr Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas
title_full_unstemmed Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas
title_short Production and characterisation of a recombinant scFv reactive with human gastrointestinal carcinomas
title_sort production and characterisation of a recombinant scfv reactive with human gastrointestinal carcinomas
topic Molecular and Cellular Pathology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2376138/
https://www.ncbi.nlm.nih.gov/pubmed/12177777
http://dx.doi.org/10.1038/sj.bjc.6600365
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