Abstract
Human glutamate dehydrogenase (GDH) gene was fused with a gene fragment encoding the nine amino acid (RKKRRQRRR) protein transduction domain of human immunodeficiency virus TAT protein in bacterial expression vector to produce genetic in-frame TAT-GDH fusion protein. The TAT-GDH protein can enter PC12 cells efficiently when added exogenously in culture media as determined by Western blot analysis and enzyme activities. Once inside the cells, the transduced denatured TAT-GDH protein showed a full activity of GDH indicating that the TAT-GDH fusion protein was correctly refolded after delivery into cells and the activities of GDH in the TAT-GDH fusion protein was not affected by the addition of the TAT sequence. TAT-GDH fusion protein and TAT itself showed no cytotoxicity in PC12 cells. Although the exact mechanism of transduction across a membrane remains unclear, the transduction activity of TAT-GDH into PC12 cells may suggest new possibilities for direct delivery of GDH into the patients with the GDH-deficient disorders.
Original language | English |
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Pages (from-to) | 37-42 |
Number of pages | 6 |
Journal | Neurochemistry International |
Volume | 41 |
Issue number | 1 |
DOIs | |
Publication status | Published - 2002 |
Bibliographical note
Funding Information:This work was supported by a National Research Laboratory (NRL) grant (M1–9911–00–0025) from the Korean Ministry of Science and Technology.
All Science Journal Classification (ASJC) codes
- Cellular and Molecular Neuroscience
- Cell Biology