WO2010145792A1 - Bispecific antigen binding proteins - Google Patents
Bispecific antigen binding proteins Download PDFInfo
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- WO2010145792A1 WO2010145792A1 PCT/EP2010/003559 EP2010003559W WO2010145792A1 WO 2010145792 A1 WO2010145792 A1 WO 2010145792A1 EP 2010003559 W EP2010003559 W EP 2010003559W WO 2010145792 A1 WO2010145792 A1 WO 2010145792A1
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- fab fragments
- antibody
- replaced
- antigen binding
- binding protein
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- NLJMYIDDQXHKNR-UHFFFAOYSA-K sodium citrate Chemical compound O.O.[Na+].[Na+].[Na+].[O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O NLJMYIDDQXHKNR-UHFFFAOYSA-K 0.000 description 1
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- UCSJYZPVAKXKNQ-HZYVHMACSA-N streptomycin Chemical compound CN[C@H]1[C@H](O)[C@@H](O)[C@H](CO)O[C@H]1O[C@@H]1[C@](C=O)(O)[C@H](C)O[C@H]1O[C@@H]1[C@@H](NC(N)=N)[C@H](O)[C@@H](NC(N)=N)[C@H](O)[C@H]1O UCSJYZPVAKXKNQ-HZYVHMACSA-N 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 230000004797 therapeutic response Effects 0.000 description 1
- 210000001685 thyroid gland Anatomy 0.000 description 1
- 238000004448 titration Methods 0.000 description 1
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- 230000009466 transformation Effects 0.000 description 1
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/46—Hybrid immunoglobulins
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/18—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans
- C07K16/22—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies against material from animals or humans against growth factors ; against growth regulators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/395—Antibodies; Immunoglobulins; Immune serum, e.g. antilymphocytic serum
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
- A61P35/02—Antineoplastic agents specific for leukemia
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal antibodies
- C07K16/46—Hybrid immunoglobulins
- C07K16/468—Immunoglobulins having two or more different antigen binding sites, e.g. multifunctional antibodies
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/11—DNA or RNA fragments; Modified forms thereof; Non-coding nucleic acids having a biological activity
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/31—Immunoglobulins specific features characterized by aspects of specificity or valency multispecific
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/30—Immunoglobulins specific features characterized by aspects of specificity or valency
- C07K2317/35—Valency
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/55—Fab or Fab'
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/50—Immunoglobulins specific features characterized by immunoglobulin fragments
- C07K2317/56—Immunoglobulins specific features characterized by immunoglobulin fragments variable (Fv) region, i.e. VH and/or VL
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/64—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising a combination of variable region and constant region components
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/60—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments
- C07K2317/66—Immunoglobulins specific features characterized by non-natural combinations of immunoglobulin fragments comprising a swap of domains, e.g. CH3-CH2, VH-CL or VL-CH1
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/73—Inducing cell death, e.g. apoptosis, necrosis or inhibition of cell proliferation
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2317/00—Immunoglobulins specific features
- C07K2317/70—Immunoglobulins specific features characterized by effect upon binding to a cell or to an antigen
- C07K2317/76—Antagonist effect on antigen, e.g. neutralization or inhibition of binding
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
Definitions
- the present invention relates to bispecific antigen binding proteins, methods for their production, pharmaceutical compositions containing said antibodies, and uses thereof.
- Engineered proteins such as bi- or multispecific antibodies capable of binding two or more antigens are known in the art.
- Such multispecific binding proteins can be generated using cell fusion, chemical conjugation, or recombinant DNA techniques.
- linkers either to fuse the antibody core (IgA, IgD, IgE, IgG or IgM) to a further binding protein (e.g. scFv) or to fuse e.g. two Fab fragments or scFv (Fischer, N., and Leger, O., Pathobiology 74 (2007) 3-14). While it is obvious that linkers have advantages for the engineering of bispecific antibodies, they may also cause problems in therapeutic settings. Indeed, these foreign peptides might elicit an immune response against the linker itself or the junction between the protein and the linker.
- CDC complement-dependent cytotoxicity
- ADCC antibody dependent cellular cytotoxicity
- bispecific antibodies that are very similar in general structure to naturally occurring antibodies (like IgA, IgD, IgE, IgG or IgM) with minimal deviation from human sequences.
- the percentage of heterodimer could be further increased by remodeling the interaction surfaces of the two CH3 domains using a phage display approach and the introduction of a disulfide bridge to stabilize the heterodimers (Merchant A. M, et al., Nature Biotech
- Another approach to circumvent the problem of mispaired byproducts in the preparation of bispecific antibodies is to switch from heterodimers to homodimers by using an full length antibody which specifically binds to a first antigen and which has fused to its heavy chains N-termini two fused Fab fragments which specifically bind to a second antigen as described e.g. in WO2001/077342.
- One important disadvantage of this strategy is the formation of undesired inactive byproducts by the mispairing of the light chains of the full length antibody with the CHl-VH domains of the Fab fragments and by the mispairing of the Fab fragment light chains with CHl-VH domains of the full length antibody.
- WO 2006/093794 relates to heterodimeric protein binding compositions.
- WO 99/37791 describes multipurpose antibody derivatives. Morrison, S., L., et al the J. Immunolog, 160(1998) 2802-2808 refers to the influence of variable region domain exchange on the functional properties of IgG.
- the invention comprises bispecific antigen binding protein, comprising:
- variable domains VL and VH are replaced by each other, 5 and the constant domains CL and CHl are replaced by each other, and in both Fab fragments of b) the variable domains VL and VH are replaced by each other, 10 or the constant domains CL and CHl are replaced by each other,
- variable domains VL and VH are replaced by each other, 15 or the constant domains CL and CHl are replaced by each other, and in both Fab fragments of b) the variable domains VL and VH are replaced by each other, 20 and the constant domains CL and CHl are replaced by each other,
- a further embodiment of the invention is a method for the preparation of an antigen binding protein according to the invention
- a further embodiment of the invention is a pharmaceutical composition comprising an antigen binding protein according to the invention and at least one pharmaceutically acceptable excipient.
- a further embodiment of the invention is a method for the treatment of a patient in need of therapy, characterized by administering to the patient a therapeutically effective amount of an antigen binding protein according to the invention.
- the invention comprises a bispecific antigen binding protein, comprising: a) two light chains and two heavy chains of an antibody, which specifically binds to a first antigen and comprises two Fab fragments; b) two additional Fab fragments of an antibody, which specifically binds to a second antigen, wherein said additional Fab fragments are fused both via a peptide connector either to the C- or N-termini of the heavy chains of a);
- variable domains VL and VH are replaced by each other, and the constant domains CL and CHl are replaced by each other, and in both Fab fragments of b) the variable domains VL and VH are replaced by each other, or the constant domains CL and CHl are replaced by each other,
- variable domains VL and VH are replaced by each other, or the constant domains CL and CHl are replaced by each other, and in both Fab fragments of b) the variable domains VL and VH are replaced by each other, and the constant domains CL and CHl are replaced by each other,
- the bispecific antigen binding protein according to the invention is characterized in that
- said additional Fab fragments are fused both via a peptide connector either to the C-termini of the heavy chains of a), or to the N-termini of the heavy chains of a).
- the bispecific antigen binding protein according to the invention is characterized in that
- said additional Fab fragments are fused both via a peptide connector either to the C-termini of the heavy chains of a).
- the bispecific antigen binding protein according to the invention is characterized in that
- said additional Fab fragments are fused both via a peptide connector to the N- termini of the heavy chains of a).
- the bispecific antigen binding protein according to the invention is characterized in that
- the bispecific antigen binding protein according to the invention is characterized in that
- Antibodies of subclass IgGl, IgG2, and IgG3 usually show complement activation including CIq and C3 binding, whereas IgG4 does not activate the complement system and does not bind CIq and/or C3.
- Cell-mediated effector functions of monoclonal antibodies can be enhanced by engineering their oligosaccharide component as described in Umana, P., et al., Nature Biotechnol. 17 (1999) 176-180, and US 6,602,684.
- IgGl type antibodies the most commonly used therapeutic antibodies, are glycoproteins that have a conserved N-linked glycosylation site at Asn297 in each CH2 domain.
- Asn297 can also be located some amino acids (usually not more than +3 amino acids) upstream or downstream of position 297, i.e. between position 294 and 300.
- the glycosylated antigen binding protein according to the invention the IgG subclass is of human IgGl subclass, of human IgGl subclass with the mutations L234A and L235A or of IgG3 subclass.
- the amount of N-glycolylneuraminic acid (NGNA) is 1% or less and/or the amount of N-terminal alpha- 1,3 -galactose is 1 % or less within said sugar chain.
- the sugar chain show preferably the characteristics of N-linked glycans attached to Asn297 of an antibody recombinantly expressed in a CHO cell.
- the sugar chains show characteristics of N-linked glycans attached to Asn297 of an antibody recombinantly expressed in a CHO cell
- NGNA as used within this application denotes the sugar residue
- N-glycolylneuraminic acid N-glycolylneuraminic acid.
- CHO type glycosylation of antibody Fc parts is e.g. described by Routier, F., H., Glycoconjugate J. 14 (1997) 201-207.
- Antibodies which are recombinantly expressed in non-glycomodified CHO host cells usually are fucosylated at Asn297 in an amount of at least 85%.
- the modified oligosaccharides of the full length parent antibody may be hybrid or complex.
- the bisected, reduced/not- fucosylated oligosaccharides are hybrid.
- the bisected, reduced/not-fucosylated oligosaccharides are complex.
- Methods for recombinant production are widely known in the state of the art and comprise protein expression in prokaryotic and eukaryotic cells with subsequent isolation of the antigen binding protein and usually purification to a pharmaceutically acceptable purity.
- nucleic acids encoding the respective modified light and heavy chains are inserted into expression vectors by standard methods.
- Amino acid sequence variants (or mutants) of the bispecific antigen binding protein are prepared by introducing appropriate nucleotide changes into the antigen binding protein DNA, or by nucleotide synthesis. Such modifications can be performed, however, only in a very limited range, e.g. as described above. For example, the modifications do not alter the above mentioned antibody characteristics such as the
- HEK 293 A preferred transient expression system (HEK 293) is described by Schlaeger, E.-J., and Christensen, K., in Cytotechnology 30 (1999) 71-83 and by Schlaeger, E.-J., in J. Immunol. Methods 194 (1996) 191-199.
- a nucleic acid is "operably linked" when it is placed in a functional relationship with another nucleic acid sequence.
- DNA for a pre-sequence or secretory leader is operably linked to DNA for a polypeptide if it is expressed as a pre-protein that participates in the secretion of the polypeptide;
- a promoter or enhancer is operably linked to a coding sequence if it affects the transcription of the sequence; or
- a ribosome binding site is operably linked to a coding sequence if it is positioned so as to facilitate translation.
- "operably linked” means that the DNA sequences being linked are contiguous, and, in the case of a secretory leader, contiguous and in reading frame.
- enhancers do not have to be contiguous. Linking is accomplished by ligation at convenient restriction sites. If such sites do not exist, the synthetic oligonucleotide adaptors or linkers are used in accordance with conventional practice. Purif ⁇ cation of antibodies is performed in order to eliminate cellular components or other contaminants, e.g. other cellular nucleic acids or proteins, by standard techniques, including alkaline/SDS treatment, CsCl banding, column chromatography, agarose gel electrophoresis, and others well known in the art. See Ausubel, F., et al., ed. Current Protocols in Molecular Biology, Greene Publishing and Wiley Interscience, New York (1987).
- affinity chromatography with microbial proteins e.g. protein A or protein G affinity chromatography
- ion exchange chromatography e.g. cation exchange (carboxymethyl resins), anion exchange (amino ethyl resins) and mixed-mode exchange
- hydrophobic interaction or aromatic adsorption chromatography e.g. with phenyl-sepharose, aza-arenophilic resins, or m-aminophenylboronic acid
- metal chelate affinity chromatography e.g. with Ni(II)- and Cu(II)-affinity material
- size exclusion chromatography e.g. with electrophoretical methods (such as gel electrophoresis, capillary electrophoresis)
- Another aspect of the invention is said pharmaceutical composition for the treatment of cancer.
- Another aspect of the invention is the bispecific antigen binding protein according to the invention for the treatment of cancer.
- Another aspect of the invention is the use of an antigen binding protein according to the invention for the manufacture of a medicament for the treatment of cancer.
- Another aspect of the invention is a method of treatment of a patient suffering from cancer by administering an antigen binding protein according to the invention to said patient in the need of such treatment.
- pharmaceutical carrier includes any and all solvents, dispersion media, coatings, antibacterial and antifungal agents, isotonic and absorption delaying agents, and the like that are physiologically compatible.
- the carrier is suitable for intravenous, intramuscular, subcutaneous, parenteral, spinal or epidermal administration (e.g. by injection or infusion).
- a composition of the present invention can be administered by a variety of methods known in the art. As will be appreciated by the skilled artisan, the route and/or mode of administration will vary depending upon the desired results. To administer a compound of the invention by certain routes of administration, it may be necessary to coat the compound with, or co-administer the compound with, a material to prevent its inactivation.
- the compound may be administered to a subject in an appropriate carrier, for example, liposomes, or a diluent.
- Pharmaceutically acceptable diluents include saline and aqueous buffer solutions.
- Pharmaceutical carriers include sterile aqueous solutions or dispersions and sterile powders for the extemporaneous preparation of sterile injectable solutions or dispersion. The use of such media and agents for pharmaceutically active substances is known in the art.
- cancer refers to proliferative diseases, such as lymphomas, lymphocytic leukemias, lung cancer, non small cell lung (NSCL) cancer, bronchioloalviolar cell lung cancer, bone cancer, pancreatic cancer, skin cancer, cancer of the head or neck, cutaneous or intraocular melanoma, uterine cancer, ovarian cancer, rectal cancer, cancer of the anal region, stomach cancer, gastric cancer, colon cancer, breast cancer, uterine cancer, carcinoma of the fallopian tubes, carcinoma of the endometrium, carcinoma of the cervix, carcinoma of the vagina, carcinoma of the vulva, Hodgkin's Disease, cancer of the esophagus, cancer of the small intestine, cancer of the endocrine system, cancer of the thyroid gland, cancer of the parathyroid gland, cancer of the adrenal gland, sarcoma of soft tissue, cancer of the urethra, cancer of the penis, prostate cancer, cancer of the bladder, cancer of the kidney or ure
- compositions may also contain adjuvants such as preservatives, wetting agents, emulsifying agents and dispersing agents. Prevention of presence of microorganisms may be ensured both by sterilization procedures, supra, and by the inclusion of various antibacterial and antifungal agents, for example, paraben, chlorobutanol, phenol, sorbic acid, and the like. It may also be desirable to include isotonic agents, such as sugars, sodium chloride, and the like into the compositions. In addition, prolonged absorption of the injectable pharmaceutical form may be brought about by the inclusion of agents which delay absorption such as aluminum monostearate and gelatin.
- the compounds of the present invention which may be used in a suitable hydrated form, and/or the pharmaceutical compositions of the present invention, are formulated into pharmaceutically acceptable dosage forms by conventional methods known to those of skill in the art.
- Actual dosage levels of the active ingredients in the pharmaceutical compositions of the present invention may be varied so as to obtain an amount of the active ingredient which is effective to achieve the desired therapeutic response for a particular patient, composition, and mode of administration, without being toxic to the patient.
- the selected dosage level will depend upon a variety of pharmacokinetic factors including the activity of the particular compositions of the present invention employed, the route of administration, the time of administration, the rate of excretion of the particular compound being employed, the duration of the treatment, other drugs, compounds and/or materials used in combination with the particular compositions employed, the age, sex, weight, condition, general health and prior medical history of the patient being treated, and like factors well known in the medical arts.
- Proper fluidity can be maintained, for example, by use of coating such as lecithin, by maintenance of required particle size in the case of dispersion and by use of surfactants.
- isotonic agents for example, sugars, polyalcohols such as mannitol or sorbitol, and sodium chloride in the composition.
- the expressions "cell,” “cell line,” and “cell culture” are used interchangeably and all such designations include progeny.
- the words “transformants” and “transformed cells” include the primary subject cell and cultures derived therefrom without regard for the number of transfers. It is also understood that all progeny may not be precisely identical in DNA content, due to deliberate or inadvertent mutations. Variant progeny that have the same function or biological activity as screened for in the originally transformed cell are included. Where distinct designations are intended, it will be clear from the context.
- transfection refers to process of transfer of a vectors/nucleic acid into a host cell. If cells without daunting cell wall barriers are used as host cells, transfection is carried out e.g. by the calcium phosphate precipitation method as described by Graham, F., L., and Van der Eb, A., J.,
- expression refers to the process by which a nucleic acid is transcribed into mRNA and/or to the process by which the transcribed mRNA (also referred to as transcript) is subsequently being translated into peptides, polypeptides, or proteins.
- the transcripts and the encoded polypeptides are collectively referred to as gene product. If the polynucleotide is derived from genomic DNA, expression in a eukaryotic cell may include splicing of the mRNA.
- a “vector” is a nucleic acid molecule, in particular self-replicating, which transfers an inserted nucleic acid molecule into and/or between host cells.
- the term includes vectors that function primarily for insertion of DNA or RNA into a cell (e.g., chromosomal integration), replication of vectors that function primarily for the replication of DNA or RNA, and expression vectors that function for transcription and/or translation of the DNA or RNA. Also included are vectors that provide more than one of the functions as described.
- Figure 1 Schematic structure of a full length antibody without CH4 domain specifically binding to a first antigen 1 with two pairs of heavy and light chain which comprise variable and constant domains in a typical order.
- Figure 2a and 2b Schematic structure of typical unmodified Fab fragments specifically binding to a second antigen 2 with the peptide connector either at the C-terminus ( Figure 2a) or
- Figure 3 Schematic structure of a full length antibody specifically binding to a first antigen 1 which has fused to the
- Figure 4a, 4b and 4c Schematic structure of a bispecific antigen binding proteins according to the invention in which the mispairing is reduced by the replacement of certain domains a) in the Fab fragment of the full length antibody which specifically binds to a first antigen 1 and/or b) in the two additional fused Fab fragments antibody which specifically binds to a second antigen 2.
- Figure 4a shows bispecific antigen binding proteins.
- Figure 4b and 4c show all combination of VH/VL and /or CHl /CL domain exchanges within the full length Fab fragments and the additional Fab fragments which lead to bispecific antigen binding proteins according to the invention with reduced mispairing.
- Figure 5 Schematic structure of a bispecific antigen binding proteins according to the invention recognizing Ang-2 and VEGF
- FIG. 1 Figure 6 Schematic structure of a bispecific antigen binding proteins according to the invention recognizing Ang-2 and VEGF (Example 2).
- DNA sequences are determined by double strand sequencing performed at MediGenomix GmbH (Martinsried, Germany) or Sequiserve GmbH (Vaterstetten, Germany).
- the transcription unit of the antibody gene is composed of the following elements: unique restriction site(s) at the 5' end
- the fusion genes comprising the described antibody chains as described below are generated by PCR and/or gene synthesis and assembled with known recombinant methods and techniques by connection of the according nucleic acid segments e.g. using unique restriction sites in the respective vectors.
- the subcloned nucleic acid sequences are verified by DNA sequencing.
- larger quantities of the plasmids are prepared by plasmid preparation from transformed E. coli cultures (Nucleobond AX, Macherey-Nagel).
- Bispecific tetravalent antibodies are expressed by transient co-transfection of the respective three expression plasmids in adherently growing HEK293-EBNA or in HEK29-F cells growing in suspension as described below. Transient transfections in HEK293-EBNA system
- Bispecific tetravalent antibodies are expressed by transient co-transfection of the respective three expression plasmids (e.g. encoding the modified heavy chain, as well as the corresponding light and modified light chain) in adherently growing HEK293-EBNA cells (human embryonic kidney cell line 293 expressing Epstein-
- Proteins are expressed from the respective plasmids using a molar ratio of (modified and wildtype) light chain and modified heavy chain encoding plasmids of 1 :1 :1 (equimolar) ranging from 1 :1 :2 to 2:2:1, respectively.
- Cells are feeded at day 3 with L-Glutamine ad 4 mM, Glucose [Sigma] and NAA [Gibco].
- Bispecific tetravalent antibody containing cell culture supernatants are harvested from day 5 to 11 after transfection by centrifugation and stored at -20°C.
- General information regarding the recombinant expression of human immunoglobulins in e.g. HEK293 cells is given in: Meissner, P. et al., Biotechnol. Bioeng. 75 (2001) 197-203. Transient transfections in HEK293-F system
- bispecific tetravalent antibodies are generated by transient transfection of the respective plasmids (e.g. encoding the modified heavy chain, as well as the corresponding light and modified light chain) using the HEK293-F system (Invitrogen) according to the manufacturer's instruction.
- HEK293- F cells growing in suspension either in a shake flask or in a stirred fermenter in serumfree FreeStyle 293 expression medium (Invitrogen) are transfected with a mix of the three expression plasmids as described above and 293fectin or fectin (Invitrogen).
- HEK293-F cells are seeded at a density of 1.0E*6 cells/mL in 600 mL and incubated at 120 rpm, 8% CO2. The day after the cells are transfected at a cell density of ca. 1.5E*6 cells/mL with ca. 42 mL mix of A) 20 mL Opti-MEM (Invitrogen) with 600 ⁇ g total plasmid DNA (1 ⁇ g/mL) encoding the modified heavy chain, the corresponding light chain and the corresponding modified light chain in an equimolar ratio and B) 20 ml Opti-MEM + 1.2 mL 293 fectin or fectin (2 ⁇ l/mL). According to the glucose consumption glucose solution is added during the course of the fermentation. The supernatant containing the secreted antibody is harvested after 5-10 days and antibodies are either directly purified from the supernatant or the supernatant is frozen and stored.
- the protein concentration of purified bispecific tetravalent antibodies and derivatives is determined by determining the optical density (OD) at 280 nm, using the molar extinction coefficient calculated on the basis of the amino acid sequence according to Pace, C, N., et al., Protein Science 4 (1995) 2411-1423.
- the concentration of bispecific tetravalent antibodies in cell culture supernatants is estimated by immunoprecipitation with Protein A Agarose-beads (Roche). 60 ⁇ L
- Protein A Agarose beads are washed three times in TBS-NP40 (50 mM Tris, pH 7.5, 150 mM NaCl, 1% Nonidet-P40). Subsequently, 1-15 mL cell culture supernatant are applied to the Protein A Agarose beads pre-equilibrated in TBS- NP40. After incubation for at 1 h at room temperature the beads are washed on an Ultrafree-MC-filter column (Amicon] once with 0.5 mL TBS-NP40, twice with 0.5 mL 2x phosphate buffered saline (2xPBS, Roche) and briefly four times with 0.5 mL 100 mM Na-citrate pH 5,0.
- TBS-NP40 50 mM Tris, pH 7.5, 150 mM NaCl, 1% Nonidet-P40.
- 1-15 mL cell culture supernatant are applied to the Protein A Agarose beads pre-equilibrated in TBS- NP40.
- Bound antibody is eluted by addition of 35 ⁇ l NuP AGE® LDS Sample Buffer (Invitrogen). Half of the sample is combined with NuP AGE® Sample Reducing Agent or left unreduced, respectively, and heated for 10 min at 70°C. Consequently, 5-30 ⁇ l are applied to an 4-12% NuP AGE® Bis-
- Tris SDS-PAGE (Invitrogen) (with MOPS buffer for non-reduced SDS-PAGE and MES buffer with NuP AGE® Antioxidant running buffer additive (Invitrogen) for reduced SDS-PAGE) and stained with Coomassie Blue.
- the concentration of bispecific tetravalent antibodies in cell culture supernatants is quantitatively measured by affinity HPLC chromatography. Briefly, cell culture supernatants containing antibodies and derivatives that bind to Protein A are applied to an Applied Biosystems Poros A/20 column in 200 mM KH2PO4, 100 mM sodium citrate, pH 7.4 and eluted from the matrix with 200 mM NaCl, 100 mM citric acid, pH 2,5 on an Agilent HPLC 1100 system. The eluted protein is quantified by UV absorbance and integration of peak areas. A purified standard
- IgGl antibody served as a standard.
- the concentration of bispecific tetravalent antibodies in cell culture supernatants is measured by Sandwich-IgG-ELISA. Briefly, StreptaWell High Bind Strepatavidin A-96 well microtiter plates (Roche) are coated with 100 ⁇ L/well biotinylated anti-human IgG capture molecule F(ab')2 ⁇ h-Fc ⁇ > BI (Dianova) at 0.1 ⁇ g/mL for 1 h at room temperature or alternatively over night at 4°C and subsequently washed three times with 200 ⁇ L/well PBS, 0.05% Tween (PBST, Sigma).
- PBST 0.05% Tween
- Protein purification Proteins are purified from filtered cell culture supernatants referring to standard protocols.
- bispecific tetravalent antibodies are applied to a Protein A Sepharose column (GE healthcare) and washed with PBS. Elution of bispecific tetravalent antibodies is achieved at pH 2.8 followed by immediate neutralization of the sample. Aggregated protein is separated from monomelic antibodies by size exclusion chromatography (Superdex 200, GE Healthcare) in PBS or in 20 mM
- Monomelic fractions are pooled, concentrated if required using e.g. a MILLIPORE Amicon Ultra (30 MWCO) centrifugal concentrator, frozen and stored at -20°C or -80°C. Part of the samples are provided for subsequent protein analytics and analytical characterization e.g. by SDS-PAGE, size exclusion chromatography or mass spectrometry.
- the NuP AGE® Pre-Cast gel system (Invitrogen) is used according to the manufacturer's instruction. In particular, 10% or 4-12% NuP AGE® Novex® Bis- TRIS Pre-Cast gels (pH 6.4) and a NuPAGE® MES (reduced gels, with NuPAGE® Antioxidant running buffer additive) or MOPS (non-reduced gels) running buffer is used.
- the total deglycosylated mass of the bispecific tetravalent antibodies is determined and confirmed via electrospray ionization mass spectrometry (ESI-MS). Briefly, 100 ⁇ g purified antibodies are deglycosylated with 50 mU N-Glycosidase F (PNGaseF, ProZyme) in 100 mM KH2PO4/K2HPO4, pH 7 at 37 0 C for 12-24 h at a protein concentration of up to 2 mg/ml and subsequently desalted via HPLC on a Sephadex G25 column (GE Healthcare). The mass of the respective modified heavy, light chain and modified light chain is determined by ESI-MS after deglycosylation and reduction.
- PNGaseF N-Glycosidase F
- bispecific tetravalent antibody in 1 15 ⁇ l are incubated with 60 ⁇ l IM TCEP and 50 ⁇ l 8 M Guanidine-hydrochloride subsequently desalted.
- the total mass and the mass of the reduced heavy and light chains is determined via ESI-MS on a Q-Star Elite MS system equipped with a NanoMate source.
- VEGF binding ELISA The binding properties of the bispecific tetravalent antibodies is evaluated in an
- VEGF165-His protein full-length VEGF165-His protein (R&D Systems).
- Falcon polystyrene clear enhanced microtiter plates are coated with 100 ⁇ l 2 ⁇ g/mL recombinant human VEGF 165 (R&D Systems) in PBS for 2 h at room temperature or over night at 4 0 C.
- the wells are washed three times with 300 ⁇ l PBST (0,2% Tween 20) and blocked with 200 ⁇ l 2% BSA 0,1% Tween 20 for 30 min at room temperature and subsequently washed three times with 300 ⁇ l PBST.
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MX2011013615A MX2011013615A (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding proteins. |
EP10725615.8A EP2443154B1 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding proteins |
CA2764392A CA2764392C (en) | 2009-06-16 | 2010-06-14 | Tetravalent bispecific antigen binding proteins |
RU2012100865/10A RU2573914C2 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen-binding proteins |
AU2010262129A AU2010262129A1 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding proteins |
BRPI1008145A BRPI1008145B8 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding protein, method for preparing a bispecific antigen binding protein, transgenic microorganism, pharmaceutical composition and use of the bispecific antigen binding protein |
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DK10725615.8T DK2443154T3 (en) | 2009-06-16 | 2010-06-14 | BISPECIFIC ANTI-ANTI-BINDING PROTEINS |
JP2012515381A JP5689463B2 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding protein |
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SI201030525T SI2443154T1 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding proteins |
PL10725615T PL2443154T3 (en) | 2009-06-16 | 2010-06-14 | Bispecific antigen binding proteins |
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ZA2011/08536A ZA201108536B (en) | 2009-06-16 | 2011-11-21 | Bispecific antigen binding proteins |
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