Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells

Recombinant antibody cloning and phage display technologies can be employed to produce and isolate single-chain antibodies (scFv) specifically against antigen of interest. The aims of this study are to construct single chain variable fragment (scFv) towards MCF-7 breast cancer cells and to character...

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Main Author: Ahmad, Zuhaida Asra
Format: Thesis
Language:English
English
Published: 2008
Online Access:http://psasir.upm.edu.my/id/eprint/5388/1/IB_2008_1.pdf
http://psasir.upm.edu.my/id/eprint/5388/
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Institution: Universiti Putra Malaysia
Language: English
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spelling my.upm.eprints.53882013-05-27T07:22:28Z http://psasir.upm.edu.my/id/eprint/5388/ Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells Ahmad, Zuhaida Asra Recombinant antibody cloning and phage display technologies can be employed to produce and isolate single-chain antibodies (scFv) specifically against antigen of interest. The aims of this study are to construct single chain variable fragment (scFv) towards MCF-7 breast cancer cells and to characterize scFv antibodies that interacts with MCF-7. Initially, mRNA was extracted from previously well-characterized monoclonal antibody (C3A8) against MCF-7. The genes encoding heavy (VH) and light (VL) chains were amplified, linked in VH-VL orientation via PCR and cloned into a pCANTAB 5E phagemid vector. The protein was then expressed in a supE strain of E. coli TG1. Phage particles displaying scFv were panned against MCF-7 and the selected clones were further used for infecting non-suppressor strain, E. coli HB2151. The scFv antibodies expressed were characterized by enzyme-linked immunosorbent assay (ELISA) and immunoblotting. As demonstrated by ELISA result, the scFv antibodies could strongly bind to MCF-7 breast cancer cells. It retained the binding capacity of its parental C3A8 monoclonal antibody. Clone B7 was expressed mainly as soluble periplasmic protein. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the recombinant antibody revealed a protein with apparent molecular weight of approximately 32 kDa. Nucleotide sequence analysis of C3A8 scFv showed high homology (99%) with published single chain antibody against rice stripe virus protein P20 [synthetic construct]. In conclusion, the recombinant antibody technology is an effective approach in the development of scFv antibody for the next generation of immunotherapy reagents especially towards MCF-7 breast cancer cells. 2008 Thesis NonPeerReviewed application/pdf en http://psasir.upm.edu.my/id/eprint/5388/1/IB_2008_1.pdf Ahmad, Zuhaida Asra (2008) Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells. Masters thesis, Universiti Putra Malaysia. English
institution Universiti Putra Malaysia
building UPM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Putra Malaysia
content_source UPM Institutional Repository
url_provider http://psasir.upm.edu.my/
language English
English
description Recombinant antibody cloning and phage display technologies can be employed to produce and isolate single-chain antibodies (scFv) specifically against antigen of interest. The aims of this study are to construct single chain variable fragment (scFv) towards MCF-7 breast cancer cells and to characterize scFv antibodies that interacts with MCF-7. Initially, mRNA was extracted from previously well-characterized monoclonal antibody (C3A8) against MCF-7. The genes encoding heavy (VH) and light (VL) chains were amplified, linked in VH-VL orientation via PCR and cloned into a pCANTAB 5E phagemid vector. The protein was then expressed in a supE strain of E. coli TG1. Phage particles displaying scFv were panned against MCF-7 and the selected clones were further used for infecting non-suppressor strain, E. coli HB2151. The scFv antibodies expressed were characterized by enzyme-linked immunosorbent assay (ELISA) and immunoblotting. As demonstrated by ELISA result, the scFv antibodies could strongly bind to MCF-7 breast cancer cells. It retained the binding capacity of its parental C3A8 monoclonal antibody. Clone B7 was expressed mainly as soluble periplasmic protein. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) analysis of the recombinant antibody revealed a protein with apparent molecular weight of approximately 32 kDa. Nucleotide sequence analysis of C3A8 scFv showed high homology (99%) with published single chain antibody against rice stripe virus protein P20 [synthetic construct]. In conclusion, the recombinant antibody technology is an effective approach in the development of scFv antibody for the next generation of immunotherapy reagents especially towards MCF-7 breast cancer cells.
format Thesis
author Ahmad, Zuhaida Asra
spellingShingle Ahmad, Zuhaida Asra
Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells
author_facet Ahmad, Zuhaida Asra
author_sort Ahmad, Zuhaida Asra
title Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells
title_short Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells
title_full Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells
title_fullStr Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells
title_full_unstemmed Construction of a Single Chain Variable Fragment Against Mcf-7 Breast Cancer Cells
title_sort construction of a single chain variable fragment against mcf-7 breast cancer cells
publishDate 2008
url http://psasir.upm.edu.my/id/eprint/5388/1/IB_2008_1.pdf
http://psasir.upm.edu.my/id/eprint/5388/
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