@article { author = {Ghaedi, Mahboobe and Sahebghadam Lotfi, Abbas and Soleimani, Masoud and Shamsara, Mehdi and Arjmand, Sare and Adibi, Behzad}, title = {Expression of Recombinant Alpha-1 Antitrypsin in CHO and COS-7 Cell Lines Using Lentiviral Vector}, journal = {Iranian Journal of Biotechnology}, volume = {7}, number = {3}, pages = {148-156}, year = {2009}, publisher = {National Institute of Genetic Engineering and Biotechnology of Iran}, issn = {1728-3043}, eissn = {2322-2921}, doi = {}, abstract = {In this study, in order to facilitate and accelerate the production of eukaryotic protein alpha 1-antitrypsin (AAT) with correct post-translational modifications, a protein production system based on the transduction of CHO and COS-7 cells using lentiviral vectors was developed. Human AAT cDNA was cloned into a replication-defective lentiviral vector. The transgene AAT-Jred chimer was transferred to CHO and COS-7 cell lines using this vector and its expressions were visualized by fluorescent microscopy. The mRNA expression levels of the AAT genes were determined using Revearse Transcriptase-Polymerase Chain Reaction (RT-PCR) and its secretion into the medium by both cell types was determined using ELISA. The results show that by employing a lentiviral vector, efficient genetic loading of CHO and COS-7 cells with the AAT gene was achieved. In conclusion, by using a Lentivirus-based gene delivery system, large amounts of recombinant human AAT protein were expressed in both CHO and COS-7 cell lines. This expression system possesses key properties that ensure its application in the delivery of therapeutic genes into mammalian cultured cells.}, keywords = {Alpha-1 antitrypsin,Transfection,Protein production,Lentiviral vector}, url = {https://www.ijbiotech.com/article_7070.html}, eprint = {https://www.ijbiotech.com/article_7070_3265ba4e828b65e6928d9148e96fe25b.pdf} }