Abstract
Human immunodeficiency virus type 1 (HIV-1) transactivator of transcription (Tat) protein possesses a unique membrane-transduction property. Interestingly, Tat transduction could be dramatically increased 1000-fold based on LTR-transactivation assay when complexed with cationic liposomes (lipo-Tat), compared with Tat alone. Therefore, underlining mechanisms were explored further. Microscopy and flow cytometry showed that this effect was associated with enhanced membrane binding, large particle formation (1-2 μm) and increased intracellular uptake of Tat fluorescent proteins. Using pharmacological assays and immune colocalizations, it was found that lipid raft-dependent endocytosis and macropinocytosis were major pathways involved in lipo-Tat uptake, and actin-filaments played a major role in intracellular trafficking of lipo-Tat to the nucleus. Furthermore, we found that the Tat hydrophobic domain (aa 36-47) mediated formation of two positively charged molecules into lipo-Tat complexes via hydrophobic bonds, based on LTR-transactivation inhibition assay. Thus, the hydrophobic domain may play an important role in Tat protein uptake and be useful for intracellular delivery of biomacromolecules if coupled together with Tat basic peptide, a cell-penetrating peptide.
Original language | English (US) |
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Pages (from-to) | 2824-2834 |
Number of pages | 11 |
Journal | FASEB Journal |
Volume | 26 |
Issue number | 7 |
DOIs | |
State | Published - Jul 2012 |
Externally published | Yes |
Keywords
- Endocytosis
- Hydrophobic peptide
- Intracellular delivery
- Transactivation
- Uptake
ASJC Scopus subject areas
- Biotechnology
- Biochemistry
- Molecular Biology
- Genetics