The Efficiency of Tat Cell Penetrating Peptide for Intracellular Uptake of HIV-1 Nef Expressed in E. coli and Mammalian Cell

• Published in: Current drug delivery Vol. 14; no. 4; p. 536
• Main Authors: Kadkhodayan, Somayeh, Bolhassani, Azam, Sadat, Seyed Mehdi, Irani, Shiva, Fotouhi, Fatemeh
• Format: Journal Article
• Language: English
• Published: United Arab Emirates 01.06.2017
• Subjects: Animals; Cell-Penetrating Peptides - chemistry; Escherichia coli; Genetic Vectors; HEK293 Cells; Humans; nef Gene Products, Human Immunodeficiency Virus - genetics; Recombinant Fusion Proteins - genetics; tat Gene Products, Human Immunodeficiency Virus - genetics; Transfection; HIV-1; Eukaryotic and prokaryotic expression systems; Tat; Nef; Delivery systems
• ISSN: 1875-5704
• DOI: 10.2174/1567201813666161006114448

Cell penetrating peptides (CPPs) or protein transduction domains (PTDs) have been known as a new field in cargo delivery. These peptides such as Tat, Pep-1 and Cady-2 are able to deliver genes and biologically active proteins to cytoplasmic compartments via the plasma membrane. In current study, the efficiency of pEGFP-N1 eukaryotic vector for expression of HIV-1 Tat- Nef fusion was evaluated in HEK-293T cells using TurboFect transfection reagent. In addition, the recombinant GST-Tat-Nef protein was generated in E. coli and transfected using two amphipathic CPPs (Pep-1 and Cady-2) into mammalian cells. The size and morphology of the CPP/GST-Tat-Nef complexes were evaluated by scanning electron microscopy (SEM), Zetasizer, and SDS-PAGE. The transfection of HIV-1 GST-Tat-Nef protein was also analyzed using SDS-PAGE and western blotting. Our data indicated that the recombinant GST-Tat-Nef protein generated in BL21 strain migrated as a clear band of ~ 52 kDa in SDS-PAGE. The results of SEM and Zetasizer confirmed the formation of protein/ Pep-1 or protein/ Cady-2 nanoparticles less than 200 nm in diameter. Tat CPP fused to Nef protein could deliver the recombinant Nef protein alone and notably by forming the noncovalent complexes with TurboFect, Pep-1 and Cady-2 as detected in western blotting. Moreover, intracellular uptake of Tat-Nef gene and subsequently its expression in mammalian cells was considerably higher than that for Nef gene. This data indicated that the Tat gene sequence could also increase the transfection of Nef gene in vitro. Generally, the Tat-Nef interaction led to enhance further gene expression and also protein delivery.