Published in Gene Therapy Weekly, December 8th, 2005
"Protein transduction therapy using poly-Arg can deliver the bioactive p53 protein into cancer cells and inhibits the proliferation of the cells. However, one disadvantage of such therapy is the short intracellular half-life of the delivered protein."
"Here," wrote H. Michiue and colleagues, Okayama University, "we generated mutant proteins in which multiple lysine residues in the C-terminal were substituted by Arg."
"The mutant proteins were effectively delivered...
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Source: Gene Therapy Weekly (2005-12-08)
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