Bispecific, tetravalent antigen binding proteins
The present invention relates to bispecific, tetravalent antigen binding proteins, methods for their production, pharmaceutical compositions containing said antibodies, and uses thereof.
1. A bispecific, tetravalent antigen binding protein, comprising:
a) a first heavy chain of a first antibody, wherein said first antibody specifically binds to a first antigen, and wherein said first heavy chain is fused through its C-terminus to the N-terminus of a moiety comprising VH-CH1 domains of said first antibody;
b) two light chains of said first antibody of a);
c) a second heavy chain of a second antibody, wherein said second antibody specifically binds to a second antigen, wherein said second heavy chain is fused through its C-terminus to the N-terminus of a moiety comprising VH-CL domains of said second antibody, and wherein the CH1 domain of said second heavy chain is replaced by the CL domain of said second antibody; and
d) two second light chains of said second antibody of c),
wherein the CL domain of each of said second light chains is replaced by the CH1 domain of said second antibody.
2. The antigen binding protein according to claim 1 , wherein
i) the CH3 domain of one of the first or second heavy chains is altered,
so that an amino acid residue in the CH3 domain of said first or second heavy chain is replaced with an amino acid residue having a larger side chain volume, thereby generating a protuberance which is positionable in a cavity within the interface of the CH3 domain of the other heavy chain
and
ii) the CH3 domain of the other heavy chain is altered,
so that an amino acid residue in the other heavy chain is replaced with an amino acid residue having a smaller side chain volume, thereby generating a cavity within which a protuberance as set forth in i) above is positionable.
3. The antigen binding protein according to claim 2 wherein said amino acid residue having a larger side chain volume is selected from the group consisting of arginine (R), phenylalanine (F), tyrosine (Y), tryptophan (W) and said amino acid residue having a smaller side chain volume is selected from the group consisting of alanine (A), serine (S), threonine (T), valine (V).
4. The antigen binding protein according to claim 3 , wherein
both CH3 domains are further altered by the introduction of cysteine (C) as amino acid in the corresponding positions of each CH3 domain such that a disulfide bridge between both CH3 domains can be formed.
5. The bispecific, tetravalent antigen binding protein according to claim 1 wherein said first antigen is Ang-2 and said second antigen is VEGF-A.
6. The bispecific, tetravalent antigen binding protein according to claim 2 wherein said first antigen is Ang-2 and said second antigen is VEGF-A.
7. The bispecific, tetravalent antigen binding protein according to claim 3 wherein said first antigen is Ang-2 and said second antigen is VEGF-A.
8. The bispecific, tetravalent antigen binding protein according to claim 4 wherein said first antigen is Ang-2 and said second antigen is VEGF-A.
9. A method for the preparation of a bispecific, tetravalent antigen binding protein according to claim 1 comprising the steps of
a) transforming a host cell with vectors comprising nucleic acid molecules encoding a bispecific, tetravalent antigen binding protein according to claim 1
b) culturing the host cell under conditions that allow synthesis of said antigen binding protein molecule; and
c) recovering said antigen binding protein molecule from said culture.
10. A host cell comprising vectors comprising nucleic acid molecules encoding a bispecific, tetravalent antigen binding protein according to claim 1 .
11. A pharmaceutical composition comprising the bispecific, tetravalent antigen binding protein according to claim 1 and at least one pharmaceutically acceptable excipient.