Kallikrein-binding “Kunitz domain” proteins and analogues thereof
View Patent ↗This invention provides: novel protein homologous of a Kunitz domain, which are capable of binding kallikrein; polynucleotides that encode such novel proteins; and vectors and transformed host cells containing these polynucleotides.
1. A method of treating edema in a mammalian subject, comprising:
administering to the subject a kallikrein inhibiting protein comprising a non-naturally occurring Kunitz domain, said Kunitz domain having disulfide bonds at Cys5-Cys55, Cys14-Cys38, and Cys30-Cys51 and further having:
amino acid number 13 selected from the group consisting of His and Pro;
amino acid number 14 as Cys;
amino acid number 16 selected from the group consisting of Ala and Gly;
amino acid number 17 selected from the group consisting of Ala, Asn, and Ser;
amino acid number 18 selected from the group consisting of His and Leu;
amino acid number 19 selected from the group consisting of Gln, Leu, and Pro,
amino acid number 31 as Glu;
amino acid number 32 selected from the group consisting of Glu and Gln;
amino acid number 34 selected from the group consisting of Ser, Thr, and Ile; and
amino acid number 39 selected from the group consisting of Gly, Glu, and Ala,
wherein the above amino acids are numbered to correspond to the numbering of amino acid residues of bovine pancreatic trypsin inhibitor (BPTI) (SEQ ID NO:1), and wherein the kallikrein inhibiting protein binds plasma kallikrein with a Ki less than 500 pM.
2. The method of claim 1 , wherein the edema is angioedema.
3. The method of claim 1 , wherein the edema is associated with sepsis.
4. The method of claim 1 , wherein the edema is associated with trauma.
5. The method of claim 1 , wherein the edema is associated with asthma.
6. The method of claim 1 , wherein the edema is hereditary edema.
7. The method of claim 1 , wherein the Kunitz domain further has:
amino acid number 15 selected from the group consisting of Lys and Arg;
wherein the above amino acids are numbered to correspond to the numbering of amino acid residues of bovine pancreatic trypsin inhibitor (BPTI) (SEQ ID NO: 1).
8. The method of claim 1 , wherein the Kunitz domain is selected from the group consisting of SEQ. ID. NO.2, SEQ. ID. NO.3, SEQ. ID. NO.4, SEQ. ID. NO.5, SEQ. ID. NO.6, SEQ. ID. NO.7, SEQ. ID. NO.8, SEQ. ID. NO.9, SEQ. ID. NO.10, SEQ. ID. NO.11, SEQ ID NO:13, SEQ ID NO:14, SEQ ID NO:17, SEQ ID NO:21, SEQ ID NO:27, SEQ ID NO:28, SEQ ID NO:64, and SEQ ID NO:66.
9. The method of claim 1 , wherein the subject is human.
10. The method of claim 1 , wherein the kallikrein inhibiting protein is administered as part of a pharmaceutical composition that further comprises a pharmaceutically acceptable carrier.
11. The method of claim 1 , wherein the kallikrein inhibiting protein binds plasma kallikrein with a Ki less than 50 pM.
12. The method of claim 1 , wherein the kallikrein inhibiting protein is administered parenterally.
13. The method of claim 12 , wherein the kallikrein inhibiting protein is administered subcutaneously.