Inhibitor-resistant urokinase

• US 5,648,253 A
• Filed: 09/08/1992
• Issued: 07/15/1997
• Est. Priority Date: 12/20/1990
• Status: Expired due to Fees

• Current Assignee: TSI Incorporated
• Original Assignee: TSI Incorporated
• Inventors: Wei, Cha-Mer
• Primary Examiner(s): JACOBSON, DIAN COOK
• Application Number:
  US07/942,157
• Time in Patent Office: 1,771 Days
• Field of Search: 435/2.5, 435/69.8, 435/172.3, 424/94.64, 930/240, 800/2
• US Class Current: 435/215
• CPC Class Codes: A01K 2217/05 Animals comprising random inserted nucleic acids (transgenic)
• CPC Class Codes: A61K 38/00 Medicinal preparations containing peptides peptides containing beta-lactam rings A61K31/00; cyclic dipeptides not having in their molecule any other peptide link than those which form their ring, e.g. piperazine-2,5-diones, A61K31/00; ergot alkaloids of the cyclic peptide type A61K31/48; containing macromolecular compounds having statistically distributed amino acid units A61K31/74; medicinal preparations containing antigens or antibodies A61K39/00; medicinal preparations characterised by the non-active ingredients, e.g. peptides as drug carriers, A61K47/00
• CPC Class Codes: C12N 9/6459 t-plasminogen activator (3.4.21.68), i.e. tPA
• CPC Class Codes: C12Y 304/21069 Protein C activated (3.4.21.69)

Abstract

Mutants of human urokinase are produced which have an altered amino acid sequence in the domain responsible for binding of plasminogen activator inhibitor(s). One example of an inhibitor resistant mutant is described in detail. Six amino acids (179-184), R H R G G S, have been deleted from the mature urokinase. The gene encoding inhibitor resistant preprourokinase is chemically synthesized according to computer-designed nucleotide sequences containing convenient restriction endonuclease cleavage sites, a signal for the initiation of translation, a sequence encoding the signal peptide of mouse whey acid protein and a complete coding sequence for mature inhibitor-resistant urokinase. The gene was used to transform cultured mouse cells to produce clones that stably incorporate the gene in the genome. Clones with high levels of expression were used as the hosts for production of this protein. Alternatively, the DNA for the inhibitor-resistant prourokinase/urokinase, in combination with a tissue specific promoter, could be introduced into fertilized embryos, the embryo implanted into a suitably prepared female of the same species, and the offspring analyzed for presence of the prourokinase/urokinase gene. The transgenic animals can then be bred and the urokinase produced in the milk.

Claims

1. A modified urokinase that cleaves plasminogen, wherein the modified urokinase is encoded by a nucleotide molecule wherein the codons encoding Arg His Arg Gly Gly Ser (SEQ ID NO:

1) at positions 179-184 have been deleted, and wherein the urokinase has a lower binding affinity for plasminogen activator inhibitor-1 than does unmodified urokinase including the amino acid sequence Arg His Arg Gly Gly Ser (SEQ ID NO;

     1).

2. The urokinase of claim 1 further comprising the signal peptide of whey acid protein.

3. The urokinase of claim 1 having a decreased affinity for plasminogen inhibitor-2.

4. The urokinase of claim 1 expressed in the milk of transgenic animals.

5. The urokinase of claim 1 having a decreased amount of glycosylation over unmodified urokinase.

6. The urokinase of claim 5 wherein the protein has fewer glycosylation sites than the unmodified urokinase.

7. The urokinase of claim 5 wherein the protein has enhanced fibrin affinity as compared to unmodified urokinase.