Heterodimer protein composition
View Patent ↗According to the present invention, a heterodimer protein composition that is composed of a first polypeptide comprising an immunoglobulin heavy chain constant region and a second polypeptide comprising CL-Fc prepared by fusion of an immunoglobulin light chain constant region (CL) and Fc region, and also has a deletion or substitution of Cys residues involved in disulfide bonds between CL and CH1, a purification method of the protein composition thereof, a preparation method of the protein composition thereof, a DNA and a vector encoding the protein composition thereof are provided.
1. A DNA encoding a heterodimer protein, the heterodimer protein being
(i) a heterodimer protein composed of
a first polypeptide comprising a heavy chain variable region (VH) and an immunoglobulin G (IgG)1 heavy chain constant region (CH), and
a second polypeptide comprising a light chain variable region (VL) and a fusion polypeptide (CL-Fc) prepared by fusion of a light chain constant region (CL) and an Fc region of IgG1,
wherein the heterodimer protein has a modification selected from the group consisting of:
(a-i) substitutions of C220S in the first polypeptide and H435R in the second polypeptide,
(b-i) substitutions of C214S and H435R in the second polypeptide,
(c-i) substitutions of C220S in the first polypeptide and C214S and H435R in the second polypeptide,
(d-i) substitutions of C220S in the first polypeptide and C220S, C214S and H435R in the second polypeptide,
(e-i) substitutions of C220S in the first polypeptide and C214S and H435R in the second polypeptide and a deletion of positions 216-220 in the second polypeptide,
(f-i) substitutions of C220S in the first polypeptide and C214S, H435R and Y436F in the second polypeptide,
(g-i) substitutions of C220S in the first polypeptide and C214S, H435R and Y436F in the second polypeptide and a deletion of positions 216-220 in the second polypeptide,
(h-i) substitutions of C220S, K332A and P331S in the first polypeptide, and C214S, K322A, P331S, H435R and Y436F in the second polypeptide and a deletion of positions 216-220 in the second polypeptide, and
(j-i) substitutions of C220S and I332E in the first polypeptide and C214S, I332E, H435R and Y436F in the second polypeptide and a deletion of positions 216-220 in the second polypeptide, numbering according to the EU index of Kabat (“the EU index”), or
(ii) a heterodimer protein composed of
a first polypeptide comprising a VH and an IgG4 CH, and
a second polypeptide comprising a VL and a CL-Fc prepared by fusion of a CL and an Fc region of IgG4,
wherein the heterodimer protein has a modification selected from the group consisting of:
(a-ii) substitutions of C1315 in the first polypeptide and C214S and H435R in the second polypeptide,
(b-ii) substitutions of C131S in the first polypeptide and C214S, H435R and Y436F in the second polypeptide,
(c-ii) substitutions of C131S and R409K in the first polypeptide and C214S, R409K, H435R and Y436F in the second polypeptide,
(d-ii) substitutions of C1315, S228P and R409K in the first polypeptide and C214S, S228P, R409K, H435R and Y436F in the second polypeptide,
(e-ii) substitutions of C131S, S228P, L235E and R409K in the first polypeptide and C214S, S228P, L235E, R409K, H435R and Y436F in the second polypeptide,
(f-ii) substitutions of C131S and R133K in the first polypeptide and C214S and H435R in the second polypeptide,
(g-ii) substitutions of C131S and R133K in the first polypeptide and C214S, H435R and Y436F in the second polypeptide,
(h-ii) substitutions of C131S, R133K and R409K in the first polypeptide and C214S, R409K, H435R and Y436F in the second polypeptide,
(j-ii) substitutions of C131S, R133K, S228P and R409K in the first polypeptide and C214S, S228P, R409K, H435R and Y436F in the second polypeptide, and
(k-ii) substitutions of C131S, R133K, S228P, L235E and R409K in the first polypeptide and C214S, S228P, L235E, R409K, H435R and Y436F in the second polypeptide, numbering according to the EU index of Kabat,
wherein in (i) and (ii), the VH of the first polypeptide and the VL of the second polypeptide forms a binding domain.
2. A transformant host cell expressing a heterodimer protein, comprising a protein expression vector including the DNA of claim 1 .
3. A method for producing a heterodimer protein, comprising
(a) culturing the transformant host cell of claim 2 in a culture medium to express the heterodimer protein; and
(b) purifying the heterodimer protein from a culture supernatant obtained in (a).
4. The DNA according to claim 1 , wherein the heterodimer protein is the heterodimer protein of (ii).
5. The DNA according to claim 1 , wherein the heterodimer protein of (ii) has a modification selected from the group consisting of (d-ii), (e-ii), (j-ii) and (k-ii).
6. The DNA according to claim 1 , wherein the heterodimer protein of (ii) has a modification selected from the group consisting of (c-ii), (d-ii), (e-ii), (h-ii), (j-ii) and (k-ii).
7. The DNA according to claim 1 , wherein the heterodimer protein of (ii) has a modification selected from the group consisting of (e-ii) and (k-ii).
8. The DNA according to claim 1 , wherein the heterodimer protein is the heterodimer protein of (i).
9. The DNA according to claim 1 , wherein the heterodimer protein of (i) has a modification selected from the group consisting of (e-i), (g-i), (h-i) and (j-i).
10. The DNA according to claim 1 , wherein the Fc region in (i) and (ii) have N-glycoside linked sugar chains bound thereto, and a content of fucose-free sugar chains is 20% or more based on the total N-glycoside linked sugar chains of the heterodimer protein.
11. The DNA according to claim 1 , wherein the first polypeptide in (i) or (ii) and/or the second polypeptide (i) or (ii) has one or more additional amino acid residue substitutions selected from the group consisting of P247I, F243L, R292P, Y300L, Y300F, P396L, T393A, H433P, S239D, S298A, A330L, 332E, E333A, K334A, L235E, P238A, N297A, K322A, P331S, K326A, S267E, H268F, S324T, K274Q, N276K, Y296F, K326W, K326Y, E333A, E333S, A339T, A339D, D356E, L358M, N384S, K392N, T394F, T394Y, V397M and V422I, numbering according to the EU Index.
12. The DNA according to claim 1 , which further comprises one or more binding proteins bound at the N-terminus and/or the C-terminus of the CH of the first polypeptide in (i) or (ii) and the CL-Fc of the second polypeptide in (i) or (ii).
13. The DNA according to claim 12 , wherein the one or more binding proteins are selected from the group consisting of an antibody variable region, a single chain Fv and a single variable domain.
14. The DNA according to claim 1 , which further comprises an immunoglobulin heavy chain variable region bound at the N-terminus and/or C-terminus of the CH of the first polypeptide in (i) and/or (ii), and an immunoglobulin light chain variable region bound at the N-terminus and/or C-terminus of the CL-Fc of the second polypeptide in (i) and/or (ii).
15. The DNA according to claim 1 , which further comprises an immunoglobulin light chain variable region bound at the N-terminus and/or C-terminus of the CH of the first polypeptide in (i) and/or (ii), and an immunoglobulin heavy chain variable region bound at the N-terminus and/or C-terminus of the CL-Fc of the second polypeptide in (i) and/or (ii).
16. The DNA according to claim 13 , wherein the heterodimer protein is selected from the group consisting of a monovalent antibody, a divalent antibody, a trivalent antibody and a tetravalent antibody.
17. The DNA according to claim 1 , which further comprises a light chain variable region or a heavy chain variable region at the N-terminus and/or the C-terminus of the first polypeptide in (i) or (ii) and/or the second polypeptide in (i) or (ii).
18. The DNA according to claim 17 , wherein the heterodimer protein is bispecific and binds to CD74 and Her2 or CD74 and CD20.
19. A DNA encoding a heterodimer protein, the heterodimer protein being
(i) a heterodimer protein composed of
a first polypeptide comprising a light chain variable region (VL) and an IgG1 heavy chain constant region (CH), and
a second polypeptide comprising a heavy chain variable region (VH) and a fusion polypeptide (CL-Fc) prepared by fusion of a light chain constant region (CL) and an Fc region of IgG1,
wherein the heterodimer protein has a modification selected from the group consisting of:
(a-i) substitutions of C220S in the first polypeptide and H35R in the second polypeptide,
(b-i) substitutions of C214S and H435R in the second polypeptide,
(c-i) substitutions of C220S in the first polypeptide and C214S and H435R in the second polypeptide,
(d-i) substitutions of C220S in the first polypeptide and C220S, C214S and H435R in the second polypeptide,
(e-i) substitutions of C220S in the first polypeptide and C214S and H435R in the second polypeptide and a deletion of positions 216-220 in the second polypeptide,
(f-i) substitutions of C220S in the first polypeptide and C214S, H435R and Y436F in the second polypeptide,
(g-i) substitutions of C220S in the first polypeptide and C214S, H435R and Y436F in the second polypeptide and a deletion of positions 216-220in the second polypeptide,
(h-i) substitutions of C220S, K332A and P331S in the first polypeptide, and C214S, K322A, P31S, H35R and Y436F in the second polypeptide and a deletion of positions 216-220 in the second polypeptide, and
(j-i) substitutions of C220S and I332E in the first polypeptide and C214S, I332E, H435R and Y436F in the second polypeptide and a deletion of positions 16-220 in the second polypeptide, numbering according to the EU index of Kabat (“the EU index”), or
(ii) a heterodimer protein composed of
a first polypeptide comprising a VL and an IgG4 CH, and
a second polypeptide comprising a VH and a CL-Fc prepared by fusion of a CL and an Fc region of IgG4,
wherein the heterodimer protein has a modification selected from the group consisting of:
(a-ii) substitutions of C131S in the first polypeptide and C214S and H435R in the second polypeptide,
(b-ii) substitutions of C131S in the first polypeptide and C214S, H435R and Y436F in the second polypeptide,
(c-ii) substitutions of C1315 and R409K in the first polypeptide and C214S, R409K, H435R and Y436F in the second polypeptide,
(d-ii) substitutions of C1315, S228P and R409K in the first polypeptide and C214S, S228P, R409K, H435R and Y436F in the second polypeptide,
(e-ii) substitutions of C131S, S228P, L235E and R409K in the first polypeptide and C214S, S228P, L235E, R409K, H435R and Y436F in the second polypeptide,
(f-ii) substitutions of C131S and R133K in the first polypeptide and C214S and H435R in the second polypeptide,
(g-ii) substitutions of C131S and R133K in the first polypeptide and C214S, H435R and Y436F in the second polypeptide,
(h-ii) substitutions of C131S, R133K and R409K in the first polypeptide and C214S, R409K, H435R and Y436F in the second polypeptide,
(j-ii) substitutions of C131S, R133K, S228P and R409K in the first polypeptide and C214S, S228P, R409K, H435R and Y436F in the second polypeptide and
(k-ii) substitutions of C131S, R133K, S228P, L235E and R409K in the first polypeptide and C214S, S228P, L235E, R409K, H435R and Y436F in the second polypeptide, numbering according to the EU index of Kabat,
wherein in (i) and (ii), the VL of the first polypeptide and the VH of the second polypeptide forms a binding domain.