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Expression of Recombinant Human Coagulation Factor VII by the Lizard Leishmania Expression System

The variety of recombinant protein expression systems have been developed as a resource of FVII gene expression. In the current study, the authors used a novel protein expression system based on the Iranian Lizard Leishmania, a trypanosomatid protozoan as a host for expression of FVII. Plasmid conta...

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Detalles Bibliográficos
Autores principales: Mirzaahmadi, Sina, Asaadi-Tehrani, Golnaz, Bandehpour, Mojgan, Davoudi, Nooshin, Tahmasbi, Leila, Hosseinzadeh, Nahid, Mirzahoseini, Hasan, Parivar, Kazem, Kazemi, Bahram
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3168907/
https://www.ncbi.nlm.nih.gov/pubmed/21912483
http://dx.doi.org/10.1155/2011/873874
Descripción
Sumario:The variety of recombinant protein expression systems have been developed as a resource of FVII gene expression. In the current study, the authors used a novel protein expression system based on the Iranian Lizard Leishmania, a trypanosomatid protozoan as a host for expression of FVII. Plasmid containing cDNA encoding full-length human FVII was introduced into Lizard Leishmania and positive transfectants were analyzed by SDS-PAGE and Western blot analysis. Furthermore, biological activity of purified protein was detected by PT assay. The recombinant strain harboring a construct was analyzed for expression of FVII at the mRNA and protein level. Purified rFVII was obtained and in order to confirm the purified compound was in fact rFVII. Western blot analysis was carried out. Clotting time in PT assay was reduced about 30 seconds with the purified rFVII. In Conclusion, this study has demonstrated, for the first time, that Leishmania cells can be used as an expression system for producing recombinant FVII.