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| Author(s): |
Daniela Flores Teruya Astudillo
Total Authors: 1
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| Document type: | Master's Dissertation |
| Press: | São Paulo. |
| Institution: | Universidade de São Paulo (USP). Escola Politécnica (EP/BC) |
| Defense date: | 2016-12-13 |
| Examining board members: |
Adriano Rodrigues Azzoni;
Soraia Attie Calil Jorge;
Lucimara Gaziola de la Torre
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| Advisor: | Adriano Rodrigues Azzoni |
| Abstract | |
One of the major bottlenecks on the development and approval of DNA vaccines in humans is the lack of an ideal gene delivery vector, which must be safe and efficient at the same time. Although safer, the non-viral vectors face a series of physical, enzymatic and diffusion barriers that limits the arrival of the endogenous gene in the nuclei of the target cells. The main goal of this work was the evaluation of the performances of the commercial non-viral vector Lipofectamine, and the recombinant protein T-Rp3, a multifunctional protein, on the delivery of the rabies virus glycoprotein (RVGP) gene to BHK-21 cells. First, the RVGP gene was inserted into the pVAX1 plasmid, and transfections using BHK-21 (Baby Hamster Kidney) cells were performed using the Lipofectamine reagent to verify the correct expression of the RVGP gene present in the new plasmid. As a positive control, the plasmid pCMV-RVGP was used. The quantitative reverse transcription (qRT-PCR) and immunofluorescence studies indicated the expression of RVGP from pVAX1RVGP, although in lower expression values in comparison to the control plasmid. In addition, a flow cytometry quantitative method to quantify and compare the expression of the RVGP in the membrane of the transfected cells was developed, confirming the previous results. With the purpose of increase, the expression of RVGP, the KOZAK consensus sequence was added to the new pVAX1RVGP plasmid, and despite of the apparent increase of RVGP expression, this could not be confirmed statistically. The experiments of gene delivery using the T-Rp3 protein were performed using a protein batch storaged in ultrafreezer for 10 months. However, the protein has shown not being stable after storage for this long period. Moreover, despite of being capable to complex pDNA after this time, T-Rp3 was not efficient in the transfection assays and tended to aggregate in high molar ratios. (AU) | |
| FAPESP's process: | 14/14404-9 - In vitro evaluation of the gene delivery of rabies virus glycoprotein gene using protein based non-viral vectors |
| Grantee: | Daniela Flores Teruya Astudillo |
| Support Opportunities: | Scholarships in Brazil - Master |