Latent fusion protein
View Patent ↗The present invention provides a method for providing latency to a pharmaceutically active agent. The method has application in overcoming the toxic effect of systemic administration of potent biological agents. The method comprises associating a fusion protein comprising a latency associated peptide and a proteolytic cleavage site with a pharmaceutically active agent. The fusion protein also has application in providing site specific activation to a latent pharmaceutically active agent.
1. An isolated nucleic acid construct encoding a fusion protein wherein said nucleic acid comprises: a first nucleic acid sequence encoding a biologically active protein; a second nucleic acid sequence encoding a heterologous latency associated peptide (LAP) comprising the precursor domain of TGFβ; and a third nucleic acid sequence encoding a proteolytic cleavage site between the first and second nucleic acid sequences.
2. The nucleic acid construct of claim 1 , wherein said biologically active protein comprises a growth factor; a differentiation factor, a cytokine, a chemokine, a trophic factor, a cytokine inhibitor, a cytokine receptor, a free-radical scavenging enzyme, a tissue inhibitor of a metalloproteinase, or an inhibitor of a serine protease.
3. The nucleic acid construct of claim 1 , wherein said first nucleic acid sequence encodes an interferon.
4. The nucleic acid construct of claim 1 , wherein said first nucleic acid sequence encodes an interleukin.
5. The nucleic acid construct of claim 1 , wherein said latency associated peptide comprises the precursor peptide of TGFβ-1,2,3,4 or 5.
6. The nucleic acid construct of claim 1 or claim 2 , wherein said proteolytic cleavage site is a matrix metalloproteinase (MMP) cleavage site.
7. A vector comprising the nucleic acid construct of claim 1 .
8. An isolated host cell comprising the vector of claim 7 .
9. A process for preparing a recombinant fusion protein comprising a biologically active protein, a LAP, and a proteolytic cleavage site, comprising culturing the host cell of claim 8 under conditions such that said fusion protein is expressed and recovering said fusion protein.