Generating targeted sequence diversity in fusion proteins
Methods of generating fusion protein variants are provided that comprise introducing sequence diversity at the junction region or regions in the fusion and allows for the generation of variants having a desired activity. Examples include immunoglobulins comprising a domain or polypeptide inserted into, or replacing, a CDR. Also provided are polynucleotides encoding a fusion protein and comprising two or more RSSs, and compositions and host cells comprising same, as well as fusion proteins variants produced by the described methods.
1. A fusion protein comprising a heterologous peptide grafted into a heavy chain CDR3 of an antibody antigen-binding domain scaffold, wherein the sequence of the heterologous peptide is selected from the group consisting of SEQ ID NOs:72-79, and 80, and wherein the heterologous peptide grafted into the heavy chain CDR3 of the fusion protein specifically binds GLP-1 Receptor (GLP-1R).
2. The fusion protein of claim 1 , wherein the heterologous peptide replaces the D segment of the heavy chain CDR3.
3. The fusion protein of claim 1 , wherein the heterologous peptide replaces the heavy chain CDR3.
4. The fusion protein of claim 1 , wherein the antibody antigen-binding domain scaffold is comprised within a full length antibody selected from the group consisting of IgA, IgA2, IgD, IgE, IgG and IgM.
5. The fusion protein of claim 1 , wherein the antibody antigen-binding domain scaffold is comprised within a full length human IgG.
6. The fusion protein of claim 1 , wherein the antibody antigen-binding domain scaffold is comprised within an antibody fragment or derivative selected from the group consisting of Fab, Fab′, F(ab′)2, Fd, Fv and single-chain Fv (scFv).
7. The fusion protein of claim 1 , wherein the antibody antigen-binding domain scaffold is comprised within a camelid antibody, a heavy chain antibody (hcAb), a single chain antibody (scAb), a shark antibody, a diabody, a nanobody or a fluorobody.
8. The fusion protein of claim 1 , wherein the heterologous peptide grafted into the heavy chain CDR3 comprises the polypeptide sequence encoded by a nucleotide sequence selected from the group consisting of SEQ ID NOs: 86-93 and 94.
9. A fusion protein comprising a heterologous peptide grafted into a heavy chain CDR3 of an antibody antigen-binding domain scaffold, wherein the sequence of the heterologous peptide is selected from the group consisting of SEQ ID NOs:19-24 and 25, and wherein the heterologous peptide grafted into the heavy chain CDR3 of the fusion protein specifically binds TPO receptor.
10. The fusion protein of claim 9 , wherein the heterologous peptide replaces the D segment of the heavy chain CDR3.
11. The fusion protein of claim 9 , wherein the heterologous peptide replaces the heavy chain CDR3.
12. The fusion protein of claim 9 , wherein the antibody antigen-binding domain scaffold is comprised within a full length antibody selected from the group consisting of IgA, IgA2, IgD, IgE, IgG and IgM.
13. The fusion protein of claim 9 , wherein the antibody antigen-binding domain scaffold is comprised within a full length human IgG.
14. The fusion protein of claim 9 , wherein the antibody antigen-binding domain scaffold is comprised within an antibody fragment or derivative selected from the group consisting of Fab, Fab′, F(ab′)2, Fd, Fv and single-chain Fv (scFv).
15. The fusion protein of claim 9 , wherein the antibody antigen-binding domain scaffold is comprised within a camelid antibody, a heavy chain antibody (hcAb), a single chain antibody (scAb), a shark antibody, a diabody, a nanobody or a fluorobody.
16. The fusion protein of claim 9 , wherein the heterologous peptide grafted into the heavy chain CDR3 comprises the polypeptide sequence encoded by a nucleotide sequence selected from the group consisting of SEQ ID NOs: 26, 27, and 81-84 and 85.