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The oncogenic kinase AKT1 is a prime therapeutic target, but its function cannot be easily researched as AKT activation in cells requires stimulation of cells with an unspecific growth factor that alters all cellular signaling. I designed a new method to deliver an already activated, phosphorylated AKT1 protein to cells that do not require the use of unspecific kinase activation or cell-damaging costly transfection reagents. I will produce a highly pre-activated AKT1 protein fused to a cell-penetrating peptide, combining genetic code expansion strategies with a novel method for protein delivery. Recombinant AKT1 can already be purchased from several companies, and I anticipate that the market for AKT1 proteins that are not only enzymatically active but can be easily delivered to cells, will be of similar or greater commercial interest.
Ilka Heinemann;Patrick O’Donoghue
Springboard Atlantic Inc.
Life Sciences
Life Sciences (not health); Biotechnology; Health and Related Sciences & Technology
The University of Western Ontario
Accelerate
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