Muteins of tear lipocalin and methods for obtaining the same
The present invention relates to novel muteins derived from human tear lipocalin. The invention also refers to a corresponding nucleic acid molecule encoding such a mutein and to a method for its generation. The invention further refers to a method for producing such a mutein. Finally, the invention is directed to a pharmaceutical composition comprising such a lipocalin mutein as well as to various uses of the mutein.
1. A method for reducing angiogenesis in a subject suffering from a disease or disorder related to abnormal blood vessel growth, comprising administering to the subject a mutein of human tear lipocalin having detectable binding affinity to a given non-natural ligand, or a pharmaceutical composition comprising such mutein, wherein at least one of the cysteine residues occurring at sequence positions corresponding to positions 61 and 153 of the linear wild type amino acid sequence of mature human tear lipocalin (SEQ ID NO: 71) is replaced by another amino acid residue and wherein at least 12 mutated amino acid residues are present at any of the sequence positions corresponding to positions 26-34, 56-58, 80, 83, 104-106, and 108 of the linear wild type amino acid sequence of mature human tear lipocalin, wherein the non-natural ligand is vascular endothelial growth factor (VEGF) or vascular endothelial growth factor receptor 2 (VEGF-R2).
2. The method of claim 1 , wherein the non-natural ligand is VEGF.
3. The method of claim 1 , wherein the non-natural ligand is VEGF-R2.
4. The method of claim 1 , wherein the mutein is conjugated with, or fused at its N-terminus or its C-terminus to, a member selected from the group consisting of an enzyme, a toxin, a protein or a protein domain, a peptide, a signal sequence, and an affinity tag.
5. The method of claim 1 , wherein the mutein is in conjugated form or as a fusion protein.
6. The method of claim 1 , wherein the mutein is conjugated with, or fused at its N-terminus or its C-terminus to, an antibody or one or more muteins of human lipocalin.
7. The method of claim 1 , wherein the mutein is fused to a moiety that extends the serum half-life of the mutein.
8. The method of claim 7 , wherein the moiety that extends the serum half-life is selected from the group consisting of an Fc part of an immunoglobulin, a CH3 domain of an immunoglobulin, a CH4 domain of an immunoglobulin, albumin or an albumin fragment, an albumin binding peptide, an albumin binding protein, and transferrin.
9. The method of claim 1 , wherein the mutein is conjugated to a label selected from the group consisting of organic molecules, enzyme labels, radioactive labels, fluorescent labels, chromogenic labels, luminescent labels, haptens, digoxigenin, biotin, metal complexes, metals, colloidal gold, and a moiety that extends the serum half-life of the mutein.
10. The method of claim 1 , wherein the mutein has the amino acid sequence as set forth in any one of SEQ ID NOs: 26-39 and 44-47.
11. The method of claim 1 , wherein the mutein comprises the following amino acid substitutions at sequence positions corresponding to the linear wild type amino acid sequence of mature human tear lipocalin (SEQ ID NO: 71): Glu 27→Gly, Phe 28→Ala, Pro 29→Leu, Glu 30→Arg, Met 31→Cys, Asn 32→Leu, Leu 33→Ala, Glu 34→Gly, Asp 80→Ile, Lys 83→Ile, Glu 104→Cys, and Lys 108→Val.
12. The method of claim 1 , wherein the mutein comprises the following amino acid substitutions at sequence positions corresponding to the linear wild type amino acid sequence of mature human tear lipocalin (SEQ ID NO: 71): Arg 26→Ser, Glu 27→Ile, Glu 30→Ser, Met 31→Gly, Asn 32→Arg, Leu 33→Ile, Glu→34 Tyr, Ile 57→Phe, Ser 58→Arg, Lys 83→Glu, Glu 104→Leu, Leu 105→Ala, His 106→Val, and Lys 108→Thr.
13. The method of claim 1 , wherein the mutein acts as a VEGF antagonist by inhibiting binding of VEGF to its receptor.
14. The method of claim 1 , wherein the disease or disorder related to abnormal blood vessel growth is selected from the group consisting of cancer, neovascular wet age-related macular degeneration (AMD), diabetic retinopathy or macular edema, retinopathy of prematurity or retinal vein occlusion.