Endotheliase-2 ligands
View Patent ↗Proteins that bind to ET2, such as immunoglobulins that inhibit ET2 with high affinity and selectivity, are provided. The ET2 binding proteins can be used to treat a variety of disorders, including angiogenesis-associated disorders.
1. An isolated antibody comprising a heavy chain (HC) immunoglobulin variable domain sequence comprising an HC CDR1, an HC CDR2, and an HC CDR3, and a light chain (LC) immunoglobulin variable domain sequence comprising an LC CDR1, an LC CDR2, and an LC CDR3, wherein all of said HC CDR1, HC CDR2, HC CDR3, LC CDR1, LC CDR2, and LC CDR3 are selected from any one antibody selected from the group consisting of A2, B5, D2, D5, F8, H10, and C9; and wherein the HC and LC immunoglobulin variable domain sequences form an antigen binding site that specifically binds to human endotheliase-2 (ET2) of SEQ ID NO:2 or SEQ ID NO:94.
2. The antibody of claim 1 , wherein the antibody accumulates at sites of angiogenesis in vivo.
3. The antibody of claim 1 , wherein the antibody inhibits proteolysis of vessel basement membrane.
4. The antibody of claim 1 , wherein the antibody inhibits angiogenesis in vitro or in vivo.
5. The antibody of claim 1 , wherein the antibody is a single chain antibody.
6. The antibody of claim 1 , wherein the antibody is a Fab fragment, a F(ab′) 2 fragment, a Fd fragments, a Fv fragment, or a dAb fragment.
7. The antibody of claim 1 , wherein the antibody is a full-length antibody.
8. The antibody of claim 1 , wherein the antibody is a human or humanized antibody.
9. The antibody of claim 1 , wherein the antibody comprises a human antibody framework region.
10. The antibody of claim 1 , wherein the antibody comprises an Fc domain.
11. The antibody of claim 1 , wherein antibody comprises the amino acid sequence of SEQ ID NO:77 and the amino acid sequence of SEQ ID NO:78.
12. A pharmaceutical composition comprising the antibody of claim 1 and a pharmaceutically acceptable carrier.
13. The antibody of claim 1 , wherein the antibody inhibits ET2 protease activity with an inhibition constant (Ki) of less than 300 nM.