Mutated anthrax toxin protective antigen proteins that...

Drug – bio-affecting and body treating compositions – Designated organic active ingredient containing – Peptide containing doai

Reexamination Certificate

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Reexamination Certificate

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07468352

ABSTRACT:
The present invention provides methods of specifically targeting compounds to cells overexpressing matrix metalloproteinases, plasminogen activators, or plasminogen activator receptors, by administering a compound and a mutant protective antigen protein comprising a matrix metalloproteinase or a plasminogen activator-recognized cleavage site in place of the native protective antigen furin-recognized cleavage site, wherein the mutant protective antigen is cleaved by a matrix metalloproteinase or a plasminogen activator overexpressed by the cell, thereby translocating into the cell a compound comprising a lethal factor polypeptide comprising a protective antigen binding site.

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Klimpel et al. (PNAS 1992; 89: 10277-10281).
Coombs et al. (J. Biol. Chem. 1998; 273: 4323-4328).
Liaw, L and Crawford, H.C., “Functions of the extracellular matrix and matrix degrading proteases during tumor progression” Braz. J. of Med. and Biol. Res. (1999) 32:805-812.
Mazar, A.P. and Jones, T.R., Abstract, XP-002131000, #146 “High-affinity, small cyclic peptide urokinase plasminogen activator receptor (uPAR)-targeting ligands localize reporter and therapeutic conjugates to the surfaces of tumor cells and stimulated endothelial cells,” Angst. Phar., 1999.

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