Abstract
Chronic Myeloid Leukaemia (CML) is a hematopoietic malignant disease characterized by the presence of the Philadelphia chromosome (Ph) (reciprocal translocation of chromosomes 22 and 9) and the formation of the BCR-ABL fusion oncoprotein, which exhibits deregulated tyrosine kinase activity. This fusion protein can be targeted using RNAi. Using viral vectors [1] and electroporation [2] has its own disadvantages. To counteract this, we resort to Cell Penetrating Peptides (CPPs). Tat has fused to membrane active peptide LK15 to form Tat-LK15 [3], that been shown to deliver DNA efficiently into cells. The efficiency was comparable to Lipofectin and PEI.
Original language | English |
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Publication status | Published - 2010 |
Event | 3rd Cellular Delivery of Therapeutic Macromolecules meeting - University of Cardiff Duration: 26 Jun 2010 → 29 Jun 2010 |
Conference
Conference | 3rd Cellular Delivery of Therapeutic Macromolecules meeting |
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City | University of Cardiff |
Period | 26/06/10 → 29/06/10 |