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Article type: Research Article
Authors: Sarina, Nurgul | Abeldenov, Sailau | Turgimbayeva, Aigerim | Zhylkibayev, Assylbek | Ramankulov, Yerlan | Khassenov, Bekbolat | Eskendirova, Saule*
Affiliations: RSE “National Center for Biotechnology” Science Committee, Ministry of Education and Science of the Republic of Kazakhstan, Astana, Kazakhstan
Correspondence: [*] Corresponding author: Saule Eskendirova, 13/5 Korgalzhyn road, Astana, 010000 Kazakhstan. Tel.: +7 7172 707524; Fax: +7 7172 707564; Cell phone: +7 702 121 3565; E-mail: [email protected].
Abstract: Human epidermal growth factor receptor 2 (HER2) is an important biomarker for detection and treatment of different types of cancers such as breast, ovarian, stomach cancer. In this study, we developed a monoclonal antibody against the extracellular domain (ECD) of HER2 biomarker of breast cancer. For this purpose, the ECD-HER2 gene was amplified and cloned into an expression vector. Gene was generated in Escherichia coli BL21 (DE3) strain for expression of recombinant protein. The expressed protein was separated by SDS-PAGE and detected by anti-his monoclonal antibody in immunoblotting. Hybridoma cells were obtained by fusing myeloma cells with mouse spleen cells injected with recombinant ECD-HER2 and screened by ELISA for the production of monoclonal antibody. The results indicate that out of three candidate hybridoma cells one clone (1E7) was producing the highest titer and antibody specificity was envisioned in ELISA results. In vivo scaling up culture of hybridoma cells in BALB/C mice lead to significant increase in the monoclonal antibody concentration up to 16 mg/ml. Immunochemical methods demonstrated the specificity of developed antibody against ECD-HER2 protein.
Keywords: Breast cancer, human epidermal growth factor 2, extracellular domain, recombinant protein, monoclonal antibody
DOI: 10.3233/HAB-170327
Journal: Human Antibodies, vol. 26, no. 2, pp. 103-111, 2018
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