Multispecific and multivalent binding proteins and uses thereof
The disclosure generally provides proteins that bind two epitopes (e.g., a first and a second epitope) and that are bivalent for binding to each of the first and second epitopes. The disclosure also provides compositions comprising such proteins, nucleic acid molecules encoding such proteins and methods of making and using such proteins.
1. A protein, comprising:
(a) a Fab arm that binds to a first epitope,
(b) a binding domain (BD) that binds to a second epitope, and
(c) an Fc region comprising CH2 and CH3 domains;
wherein the protein comprises a chimeric heavy chain comprising the following polypeptide domains, from N-terminus to C-terminus
VH1-CH1-L1-BD-L2-Fc;
wherein VH1 comprises the heavy chain variable domain of the Fab, CH1 comprises the heavy chain constant domain 1 of the Fab, L1 comprises the first linker polypeptide, BD comprises an scFV, L2 comprises the second linker polypeptide, and Fc comprises a CH2 and a CH3 domain and wherein the protein is bivalent for binding to each of the first and second epitopes, and wherein the L1 comprises the amino acid sequence EPKSCDKT (SEQ ID NO: 4) or EPKSCGKT (SEQ ID NO: 6) or EPKSC (SEQ ID NO: 38) wherein the L2 comprises the amino acid sequence EPKSVDKTHTCPPCP (SEQ ID NO: 12), CPPCP (SEQ ID NO: 14) or DKTHTCPPCP (SEQ ID NO: 40), and wherein the first epitope is selected from the group consisting of EGFR, IGFR1, VEGF, angiopoietin-2 (Ang2), exopolysaccharide (Psl) and Pseudomonas aeruginosa (Per V) and wherein the second epitope is selected from the group consisting of EGFR, IGFR1, VEGF, angiopoietin-2 (Ang2), exopolysaccharide (Psl) and Pseudomonas aeruginosa (Per V).
2. The protein of claim 1 , wherein the L1 further comprises a Gly-Ser peptide and/or wherein the L2 further comprises a linker portion comprising a Gly-Ser peptide.
3. The protein of claim 1 , wherein the scFv comprises a VH domain, a polypeptide linker and a VL domain.
4. The protein of claim 1 , wherein the Fc region is selected from the group consisting of an Fc region from an IgG1, IgG2, IgG3, IgG4, IgA, IgM, IgE, and IgD.
5. The protein of claim 4 , wherein the Fc region is aglycosylated.
6. The protein of claim 4 , wherein the Fc region is deglycosylated.
7. The protein of claim 4 , wherein the Fc region has reduced fucosylation or is afucosylated.
8. The protein of claim 4 , wherein the Fc region comprises a substitution at position 297.
9. The protein of claim 8 , wherein the substitution at position 297 is 297Q.
10. The protein of claim 1 , wherein the first and second epitopes are different or wherein the first and second epitopes are the same.
11. The protein of claim 1 , wherein the CH1 domain of the Fab arm comprises a substitution at one or more of positions 131, 132, 134, 135, 136 and 139, as numbered by the EU index and wherein the substitution is selected from the group consisting of amino acid cysteine, lysine, tyrosine, histidine, selenocysteine and selenomethionine.
12. The protein of claim 11 , wherein the substitution is a cysteine.
13. The protein of claim 1 , wherein the scFv comprises, from N-terminus to C-terminus
VH2-polypeptide linker-VL2 or VL2-polypeptide linker-VH2;
wherein VH2 comprises the heavy chain variable domain of the scFv and VL2 comprises the light chain variable domain of the scFv.
14. The protein of claim 13 , wherein the VL2 has a cysteine at Kabat position 100.
15. The protein of claim 13 , wherein the VH domain of the scFv has a cysteine at Kabat position 44.
16. The protein of claim 1 , wherein the first and second epitopes are different.
17. The protein of claim 1 , wherein the first and second epitopes are the same.
18. A composition comprising the protein of claim 1 formulated in a pharmaceutically acceptable carrier.