Protection of endogenous therapeutic peptides from peptidase activity through conjugation to blood components

• US 6,887,470 B1
• Filed: 09/07/2000
• Issued: 05/03/2005
• Est. Priority Date: 09/10/1999
• Status: Expired due to Fees

• Current Assignee: ConjuChem LLC (Colabor Group, Inc.)
• Original Assignee: ConjuChem, Inc. (Colabor Group, Inc.)
• Inventors: Bridon, Dominique P., Thibaudeau, Karen, Milner, Peter G., Ezrin, Alan M., Holmes, Darren L.
• Primary Examiner(s): Weber, Jon
• Assistant Examiner(s): Snedden, Sheridan
• Application Number:
  US09/657,276
• Time in Patent Office: 1,699 Days
• Field of Search: 424/133.1, 424/136.1, 424/9.1, 424/178, 424/1.69, 530/350, 530/387.1, 530/387.3, 530/300, 514/2
• US Class Current: 424/133.1
• CPC Class Codes: C07K 19/00 Hybrid peptides , i.e. peptides covalently bound to nucleic acids, or non-covalently bound protein-protein complexes

Abstract

A method for protecting a peptide from peptidase activity in vivo, the peptide being composed of between 2 and 50 amino acids and having a C-terminus and an N-terminus and a C-terminus amino acid and an N-terminus amino acid is described. In the first step of the method, the peptide is modified by attaching a reactive group to the C-terminus amino acid, to the N-terminus amino acid, or to an amino acid located between the N-terminus and the C-terminus, such that the modified peptide is capable of forming a covalent bond in vivo with a reactive functionality on a blood component. In the next step, a covalent bond is formed between the reactive group and a reactive functionality on a blood component to form a peptide-blood component conjugate, thereby protecting said peptide from peptidase activity. The final step of the method involves the analyzing of the stability of the peptide-blood component conjugate to assess the protection of the peptide from peptidase activity.

Claims

1. A method for selecting a therapeutic peptide protected from peptidase degradation in vivo from a plurality of therapeutic peptides comprising between 3 and 50 amino acids, the therapeutic peptides having a carboxy terminus and an amino terminus, and a carboxy terminal amino acid and an amino terminal amino acid, said peptides having been modified by coupling a reactive group to the carboxy terminal amino acid, to the amino terminal amino acid, or to an amino acid located between the amino terminal amino acid and the carboxy terminal amino acid;

the method comprising;

a) forming a covalent bond between said reactive group and a reactive functionality on non-denatured albumin to form peptide-albumin conjugates;

b) analyzing the stability of said peptide-albumin conjugates toward peptidase degradation to find one or more peptide-albumin conjugates having a higher stability to peptidase degradation than the unconjugated therapeutic peptide and verifying if the peptide-albumin conjugates retain the therapeutic activity of the unconjugated therapeutic peptide; and

c) selecting a therapeutic peptide that has a higher stability toward peptidase degradation when conjugated to albumin than the unconjugated therapeutic peptide, in accordance with step a), and retains the therapeutic activity of the unconjugated therapeutic peptide, in accordance with step b).

2. The method according to claim 1, wherein the peptide-albumin conjugates are formed in vivo.

3. The method according to claim 1, wherein the peptide albumin conjugates are formed ex vivo.

4. The method according to claim 1, wherein said reactive group comprises a maleimide group.

5. The method according to claim 1, wherein said reactive group is coupled to said peptide via a lysine and/or a linking group.

6. The method according to claim 1, wherein one or more of said amino acids is synthetic.

7. The method according to claim 1 wherein the reactive group is coupled to the therapeutic peptide at the amino terminal amino acid of the peptide.

8. The method according to claim 1 wherein the reactive group is coupled to the therapeutic peptide at the carboxy terminal amino acid of the peptide.

9. The method according to claim 1 wherein the reactive group is coupled to the therapeutic peptide at an amino acid located between the amino terminal amino acid and the carboxy terminal amino acid of the peptide.