Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K16/00—Immunoglobulins [IGs], e.g. monoclonal or polyclonal 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
  • C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
  • C12N15/1034—Isolating an individual clone by screening libraries
  • C12N15/1086—Preparation or screening of expression libraries, e.g. reporter assays
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  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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  • 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
  • C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
  • C12N15/79—Vectors or expression systems specially adapted for eukaryotic hosts
  • C12N15/85—Vectors or expression systems specially adapted for eukaryotic hosts for animal cells
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  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
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  • C12N5/00—Undifferentiated human, animal or plant cells, e.g. cell lines; Tissues; Cultivation or maintenance thereof; Culture media therefor
  • C12N5/06—Animal cells or tissues; Human cells or tissues
  • C12N5/0602—Vertebrate cells
  • C12N5/0634—Cells from the blood or the immune system
  • C12N5/0635—B lymphocytes
• • C—CHEMISTRY; METALLURGY
  • C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
  • C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
  • C12P21/00—Preparation of peptides or proteins
  • C12P21/02—Preparation of peptides or proteins having a known sequence of two or more amino acids, e.g. glutathione
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07K—PEPTIDES
  • C07K2317/00—Immunoglobulins specific features
  • C07K2317/10—Immunoglobulins specific features characterized by their source of isolation or production
  • C07K2317/14—Specific host cells or culture conditions, e.g. components, pH or temperature
• • 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
  • 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
  • C12N2510/00—Genetically modified cells
  • C12N2510/02—Cells for production

Definitions

• the hybridoma technology developed by Koehler and Milstein is widely used. But in the hybridoma technology only a fraction of the B-cells obtained from an immunized experimental animal can be fused and propagated.
• the source of the B-cells is generally an organ of an immunized experimental animal such as the spleen.
• Zubler et al. started in 1984 to develop a different approach for obtaining cells secreting monoclonal antibodies (see e.g. Eur. J. Immunol. 14 (1984) 357-363, J. Exp. Med. 160 (1984) 1170-1183).
• the B-cells are obtained from the blood of the immunized experimental animal and co-cultivated with murine EL-4 B5 feeder cells in the presence of a cytokine comprising feeder mix. With this methodology up to 50 ng/ml antibody can be obtained after 10-12 days of co-cultivation.
• the isolation of nucleic acid fragments or segments encoding antibody variable domains (light and heavy chain) and the insertion of the isolated nucleic acid fragments or segments in eukaryotic expression cassettes (one cassette each for the light and heavy chain, respectively) is performed without the intermediate isolation and analysis of clonal intermediate plasmids/cassettes.
• the intermediate cloning, isolation and analysis of intermediate plasmids/cassettes is not required, e.g. by analysis of isolated transformed E. coli cells, thus, resulting in a faster method.
• One aspect as reported herein is a method for the isolation of nucleic acids encoding cognate variable domains of an antibody comprising the following steps:
• the method is performed without the isolation and analysis of intermediate nucleic acids.
• One aspect as reported herein is a method for producing an antibody comprising the following step:
• the PCR primer are removed after the PCR.
• the method is performed without the isolation and analysis of intermediate nucleic acids.
• One aspect as reported herein is a method for producing an antibody comprising the following step:
• One aspect as reported herein is a method for producing an antibody comprising the following step:
• the PCR primer are removed after the PCR.
• the method is performed without the isolation and analysis of intermediate nucleic acids.
• One aspect as reported herein is a method for producing an antibody comprising the following step:
• the PCR primer are removed after the PCR.
• the method is performed without the isolation and analysis of intermediate nucleic acids.
• the B-cell is a rabbit B-cell.
• the B-cell is a single deposited B-cell.
• the B-cell is cultivated for about 7 days.
• the B-cell and its progeny produces more than 20 ng/ml antibody in 7 days of co-cultivation with feeder cells starting from a single cell.
• the PCR primer have the nucleic acid sequences of SEQ ID NO: 5 and 6 or SEQ ID NO: 7 or 8.
• nucleic acid fragments are inserted into the expression plasmid by sequence and ligation independent cloning.
• 300 ng nucleic acid is used in the insertion reaction.
• a pool of nucleic acids is used for the insertion.
• the expression plasmid is obtained by sequence and ligation independent cloning of the variable domain encoding nucleic acid into a variable domain free amplified expression plasmid.
• the plasmid is linearized prior to the amplification.
• Bind refers to the strength of the total sum of non-covalent interactions between a single binding site of a molecule (e.g., an antibody) and its binding partner (e.g., an antigen).
• binding affinity refers to intrinsic binding affinity which reflects a 1:1 interaction between members of a binding pair (e.g., antibody and antigen).
• the affinity of a molecule X for its partner Y can generally be represented by the dissociation constant (Kd). Affinity can be measured by common methods known in the art, including those described herein. Specific illustrative and exemplary embodiments for measuring binding affinity are described in the following.
• amino acid denotes the group of carboxy ⁇ -amino acids, which directly or in form of a precursor can be encoded by a nucleic acid.
• the individual amino acids are encoded by nucleic acids consisting of three nucleotides, so called codons or base-triplets. Each amino acid is encoded by at least one codon. This is known as “degeneration of the genetic code”.
• amino acid denotes the naturally occurring carboxy ⁇ -amino acids comprising alanine (three letter code: ala, one letter code: A), arginine (arg, R), asparagine (asn, N), aspartic acid (asp, D), cysteine (cys, C), glutamine (gln, Q), glutamic acid (glu, E), glycine (gly, G), histidine (his, H), isoleucine (ile, I), leucine (leu, L), lysine (lys, K), methionine (met, M), phenylalanine (phe, F), proline (pro, P), serine (ser, S), threonine (thr, T), tryptophan (trp, W), tyrosine (tyr, Y), and valine (val, V).
• antibody herein is used in the broadest sense and encompasses various antibody structures, including but not limited to monoclonal antibodies, polyclonal antibodies, multispecific antibodies (e.g., bispecific antibodies), and antibody fragments so long as they exhibit the desired antigen-binding activity.
• antibody fragment refers to a molecule other than an intact antibody that comprises a portion of an intact antibody that binds the antigen to which the intact antibody binds.
• antibody fragments include but are not limited to Fv, Fab, Fab′, Fab′-SH, F(ab′) 2 ; diabodies; linear antibodies; single-chain antibody molecules (e.g. scFv); single domain antibodies; and multispecific antibodies formed from antibody fragments.
• the “class” of an antibody refers to the type of constant domain or constant region possessed by its heavy chain.
• IgA, IgD, IgE, IgG, and IgM there are five major classes of antibodies in the human: IgA, IgD, IgE, IgG, and IgM, and several of these may be further divided into subclasses (isotypes), e.g., IgG1, IgG2, IgG3, IgG4, IgA1, and IgA2.
• the heavy chain constant domains that correspond to the different classes of immunoglobulins are called ⁇ , ⁇ , ⁇ , ⁇ , and ⁇ , respectively.
• cognate pair of antibody variable domains denotes a pair of antibody variable domains that is obtained from a single antibody secreting B-cell, i.e. which has been generated as pair during the immune response of a mammal due to the contact with an immunogenic molecule or which have been assembled randomly during a display approach.
• an “effective amount” of an agent refers to an amount effective, at dosages and for periods of time necessary, to achieve the desired therapeutic or prophylactic result.
• the term “expression” as used herein refers to transcription and/or translation and secretion processes occurring within a cell.
• the level of transcription of a nucleic acid sequence of interest in a cell can be determined on the basis of the amount of corresponding mRNA that is present in the cell.
• mRNA transcribed from a sequence of interest can be quantified by qPCR or RT-PCR or by Northern hybridization (see Sambrook, et al., Molecular Cloning: A Laboratory Manual, Second Edition, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y. (1989)).
• Polypeptides encoded by a nucleic acid can be quantified by various methods, e.g.
• An “expression cassette” denotes a construct that contains the necessary regulatory elements, such as promoter and polyadenylation site, for expression of at least the contained nucleic acid in a cell.
• expression machinery denotes the sum of the enzymes, cofactors, etc. of a cell that is involved in the steps of gene expression beginning with the transcription step of a nucleic acid or gene (i.e. also called “gene expression machinery”) to the post-translational modification of the polypeptide encoded by the nucleic acid.
• the expression machinery e.g. comprises the steps of transcription of DNA into pre-mRNA, pre-mRNA splicing to mature mRNA, translation into a polypeptide of the mRNA, and post translational modification of the polypeptide.
• an “expression plasmid” is a nucleic acid providing all required elements for the expression of the comprised structural gene(s) in a host cell.
• an expression plasmid comprises a prokaryotic plasmid propagation unit, e.g. for E. coli , comprising an origin of replication, and a selectable marker, a eukaryotic selection marker, and one or more expression cassettes for the expression of the structural gene(s) of interest each comprising a promoter, a structural gene, and a transcription terminator including a polyadenylation signal.
• Gene expression is usually placed under the control of a promoter, and such a structural gene is said to be “operably linked to” the promoter.
• a regulatory element and a core promoter are operably linked if the regulatory element modulates the activity of the core promoter.
• host cell refers to cells into which exogenous nucleic acid has been introduced, including the progeny of such cells.
• Host cells include “transformants” or “transfectants” and “transformed cells” and “transfected cells” which include the primary transformed cell and progeny derived therefrom without regard to the number of passages.
• Progeny may not be completely identical in nucleic acid content to a parent cell, but may contain mutations. Mutant progeny that have the same function or biological activity as screened or selected for in the originally transformed cell are included herein.
• cell includes both prokaryotic cells, which are used for propagation of plasmids, and eukaryotic cells, which are used for the expression of a nucleic acid.
• the eukaryotic cell is a mammalian cell.
• the mammalian cell is selected from the group of mammalian cells comprising CHO cells (e.g. CHO K1, CHO DG44), BHK cells, NSO cells, Sp2/0 cells, HEK 293 cells, HEK 293 EBNA cells, PER.C6® cells, and COS cells.
• a “human antibody” is one which possesses an amino acid sequence which corresponds to that of an antibody produced by a human or a human cell or derived from a non-human source that utilizes human antibody repertoires or other human antibody-encoding sequences. This definition of a human antibody specifically excludes a humanized antibody comprising non-human antigen-binding residues.
• an “individual” or “subject” is a vertebrate.
• the vertebrate is a mammal. Mammals include, but are not limited to, domesticated animals (e.g., cows, sheep, cats, dogs, and horses), primates (e.g., humans and non-human primates such as monkeys), rabbits, and rodents (e.g., mice and rats).
• the individual or subject is a human. In other embodiments the individual or subject is a rabbit.
• “Operably linked” refers to a juxtaposition of two or more components, wherein the components so described are in a relationship permitting them to function in their intended manner.
• a promoter and/or enhancer are operably linked to a coding sequence, if it acts in cis to control or modulate the transcription of the linked sequence.
• the DNA sequences that are “operably linked” are contiguous and, where necessary to join two protein encoding regions such as a secretory leader and a polypeptide, contiguous and in (reading) frame.
• an operably linked promoter is generally located upstream of the coding sequence, it is not necessarily contiguous with it. Enhancers do not have to be contiguous.
• An enhancer is operably linked to a coding sequence if the enhancer increases transcription of the coding sequence.
• Operably linked enhancers can be located upstream, within or downstream of coding sequences and at considerable distance from the promoter.
• a polyadenylation site is operably linked to a coding sequence if it is located at the downstream end of the coding sequence such that transcription proceeds through the coding sequence into the polyadenylation sequence.
• a translation stop codon is operably linked to an exonic nucleic acid sequence if it is located at the downstream end (3′ end) of the coding sequence such that translation proceeds through the coding sequence to the stop codon and is terminated there.
• Linking is accomplished by recombinant methods known in the art, e.g., using PCR methodology and/or by ligation at convenient restriction sites. If convenient restriction sites do not exist, then synthetic oligonucleotide adaptors or linkers are used in accord with conventional practice.
• peptide linker denotes amino acid sequences of natural and/or synthetic origin. They consist of a linear amino acid chain wherein the 20 naturally occurring amino acids are the monomeric building blocks.
• the peptide linker has a length of from 1 to 50 amino acids, in one embodiment between 1 and 28 amino acids, in a further embodiment between 2 and 25 amino acids.
• the peptide linker may contain repetitive amino acid sequences or sequences of naturally occurring polypeptides.
• the linker has the function to ensure that polypeptides conjugated to each other can perform their biological activity by allowing the polypeptides to fold correctly and to be presented properly.
• the peptide linker is rich in glycine, glutamine, and/or serine residues. These residues are arranged e.g.
• GS SEQ ID NO: 1
• GGS GGS
• GGGS SEQ ID NO: 3
• GGGGS GGGGS
• the small repetitive unit may be repeated for one to five times.
• amino acids At the amino- and/or carboxy-terminal ends of the multimeric unit up to six additional arbitrary, naturally occurring amino acids may be added.
• Other synthetic peptidic linkers are composed of a single amino acid, which is repeated between 10 to 20 times and may comprise at the amino- and/or carboxy-terminal end up to six additional arbitrary, naturally occurring amino acids. All peptidic linkers can be encoded by a nucleic acid molecule and therefore can be recombinantly expressed. As the linkers are themselves peptides, the polypeptide connected by the linker are connected to the linker via a peptide bond that is formed between two amino acids.
• Percent (%) amino acid sequence identity with respect to a reference polypeptide sequence is defined as the percentage of amino acid residues in a candidate sequence that are identical with the amino acid residues in the reference polypeptide sequence, after aligning the sequences and introducing gaps, if necessary, to achieve the maximum percent sequence identity, and not considering any conservative substitutions as part of the sequence identity. Alignment for purposes of determining percent amino acid sequence identity can be achieved in various ways that are within the skill in the art, for instance, using publicly available computer software such as BLAST, BLAST-2, ALIGN or Megalign (DNASTAR) software. Those skilled in the art can determine appropriate parameters for aligning sequences, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared.
• % amino acid sequence identity values are generated using the sequence comparison computer program ALIGN-2.
• the ALIGN-2 sequence comparison computer program was authored by Genentech, Inc., and the source code has been filed with user documentation in the U.S. Copyright Office, Washington D.C., 20559, where it is registered under U.S. Copyright Registration No. TXU510087.
• the ALIGN-2 program is publicly available from Genentech, Inc., South San Francisco, Calif., or may be compiled from the source code.
• the ALIGN-2 program should be compiled for use on a UNIX operating system, including digital UNIX V4.0D. All sequence comparison parameters are set by the ALIGN-2 program and do not vary.
• % amino acid sequence identity of a given amino acid sequence A to, with, or against a given amino acid sequence B is calculated as follows:
• polypeptide is a polymer consisting of amino acids joined by peptide bonds, whether produced naturally or synthetically. Polypeptides of less than about 25 amino acid residues may be referred to as “peptides”, whereas molecules consisting of two or more polypeptides or comprising one polypeptide of more than 100 amino acid residues may be referred to as “proteins”.
• a polypeptide may also comprise non-amino acid components, such as carbohydrate groups, metal ions, or carboxylic acid esters. The non-amino acid components may be added by the cell, in which the polypeptide is expressed, and may vary with the type of cell. Polypeptides are defined herein in terms of their amino acid backbone structure or the nucleic acid encoding the same. Additions such as carbohydrate groups are generally not specified, but may be present nonetheless.
• a “structural gene” denotes the region of a gene without a signal sequence, i.e. the coding region.
• variable region refers to the domain of an antibody heavy or light chain that is involved in binding the antibody to antigen.
• the variable domains of the heavy chain and light chain (VH and VL, respectively) of a native antibody generally have similar structures, with each domain comprising four conserved framework regions (FRs) and three hypervariable regions (HVRs).
• FRs conserved framework regions
• HVRs hypervariable regions
• antibodies that bind a particular antigen may be isolated using a VH or VL domain from an antibody that binds the antigen to screen a library of complementary VL or VH domains, respectively (see, e.g., Portolano, S., et al., J. Immunol. 150 (1993) 880-887; Clackson, T., et al., Nature 352 (1991) 624-628).
• variant denotes variants of a parent amino acid sequence that comprises one or more amino acid substitution, addition, or deletion.
• vector denotes a nucleic acid molecule capable of propagating another nucleic acid to which it is linked.
• the term includes the vector as a self-replicating nucleic acid structure as well as the vector incorporated into the genome of a host cell into which it has been introduced.
• Certain vectors are capable of directing the expression of nucleic acids to which they are operatively linked. Such vectors are referred to herein as “expression vectors”.
• non-human animals such as mice, rabbits, hamster and rats
• animal model for evaluating antibody based therapies.
• non-human animals such as mice, rabbits, hamster and rats
• B-cells of a human that survived a specific disease, that suffers from a chronic disease, or that was recently vaccinated against a specific disease.
• B-cells obtained from e.g. mouse, rat, hamster, rabbit, sheep, llama, or human can be used.
• the mouse is an NMRI-mouse or a balb/c-mouse.
• the hamster is selected from Armenian hamster ( Cricetulus migratorius ), Chinese hamster ( Cricetulus griseus ), and Syrian hamster ( Mesocricetulus auratus ).
• the hamster is the Armenia hamster.
• the rabbit is selected from New Zealand White (NZW) rabbits, Zimmermann-rabbits (ZIKA), Alicia-mutant strain rabbits, basilea mutant strain rabbits, transgenic rabbits with a human immunoglobulin locus, rabbit IgM knock-out rabbits, and cross-breeding thereof.
• NZW New Zealand White
• ZIKA Zimmermann-rabbits
• Alicia-mutant strain rabbits basilea mutant strain rabbits
• transgenic rabbits with a human immunoglobulin locus rabbit IgM knock-out rabbits
• rabbit IgM knock-out rabbits and cross-breeding thereof.
• the experimental animals e.g. mice, hamsters, rats and rabbits, chosen for immunization are not older than 12 weeks.
• the blood of an experimental animal or a human provides a high diversity of antibody producing B-cells.
• the therefrom obtained B-cells secrete antibodies that have almost no identical or overlapping amino acid sequences within the CDRs, thus, show a high diversity.
• the B-cells of an experimental animal or a human are obtained from 4 days after immunization until at least 9 days after immunization or the most recent boost immunization.
• This time span allows for a high flexibility in the method as reported herein. In this time span it is likely that the B-cells providing for the most affine antibodies migrate from spleen to blood (see e.g. Paus, D., et al., JEM 203 (2006) 1081-1091; Smith, K. G. S., et al., The EMBO J. 16 (1997) 2996-3006; Wrammert, J., et al., Nature 453 (2008) 667-672).
• B-cells from the blood of an experimental animal or human may be obtained with any method known to a person skilled in the art.
• density gradient centrifugation DGC
• red blood cell lysis lysis
• Density gradient centrifugation compared to lysis provides for a higher overall yield, i.e. number of B-cell clones.
• concentration of secreted antibody is higher compared to cells obtained with a different method. Therefore, in one embodiment the provision of a population of B-cells is by density gradient centrifugation.
• the total mRNA can be isolated and transcribed to cDNA.
• specific primers the cognate VH- and VL-region encoding nucleic acids can be amplified. With the method as reported herein almost no identical sequences will be obtained. Thus, the method provides for highly diverse antibodies binding to the same antigen.
• the methods as reported herein are for producing an antibody comprising cognate antibody variable domains.
• the cognate antibody variable domains are from a single B-cell.
• Primer can be provided for the amplification of the VH-encoding nucleic acid obtained from B-cells of the NMRI-mouse, the Armenian Hamster, the Balb/c-mouse, the Syrian hamster, the rabbit, the rat, the sheep, the llama, and the human.
• One aspect as reported herein is a method for producing an antibody comprising the following steps:
• the isolation of nucleic acid segments encoding antibody variable domains (light and heavy chain) and the insertion of the isolated nucleic acid segments in eukaryotic expression plasmids is performed without the intermediate isolation and analysis of clonal intermediate plasmids.
• the intermediate cloning, isolation and analysis of intermediate cassettes/plasmids is not required, e.g. by analysis of isolated transformed E. coli cells.
• the methods as reported herein are performed without the intermediate isolation and analysis of clonal intermediate plasmids.
• nucleic acid fragments encoding the heavy and light chain variable domain of an antibody as obtained after a specific polymerase chain reaction can be inserted into eukaryotic expression constructs, one for each chain, respectively, and expanded without the requirement of intermediate plating in order to pick and analyze plasmid DNA obtained from single colonies of transformed bacteria.
• a restriction endonuclease cleavage site is engineered into both sense and antisense primer, respectively, allowing the insertion of the PCR fragments into an appropriately designed expression vector.
• the relatively high promiscuity of the ligation process results in a comparatively high number of individual plasmid clones containing no inserted nucleic acid fragment (“empty vector”), containing a nucleic acid fragment inserted in the wrong direction, or containing only an incomplete fragment of the nucleic acid to be cloned. This problem usually is solved by plating the ligation reaction on solid media in such a way that individual bacterial colonies can be isolated.
• the entire workflow from the initial generation and cloning of the DNA fragments into expression vectors until the recombinant expression of the polypeptides encoded by the respective plasmid vectors can be performed in one coherent workflow without the need for intermediate isolation and analysis of single colonies. It has been found that it is advantageous to employ ligation-independent cloning as a means to improve the above-outlined workflow.
• the inserting in the eukaryotic expression plasmid is by ligation-independent cloning.
• Ligation-independent cloning as such is not necessarily more efficient than conventional cloning via restriction and ligation in the sense that the number of individual colonies obtained is significantly higher. But since this method is based on sequence-specific annealing of complementary single-stranded DNA overhangs rather than enzymatic ligation for the assembly of complex molecules, this method comprises significantly longer complementary single-stranded ends of the individual nucleic acid fragments to be cloned. Thus, typically single-stranded nucleotide overhangs encompassing 15-30 nucleotides are used in ligation-independent cloning versus 2-4 nucleotides generated by restriction endonucleases.
• the method as reported herein can be performed with B-cells obtained at any point in time after the immunization of an experimental animal.
• the method as reported herein can be performed early after immunization so that first antibody-encoding nucleic acids can be isolated as early as three weeks after the first immunization of an experimental animal.
• variable domain-encoding nucleic acid fragments from rabbit B-cells since hybridomas derived from rabbit B-cells result in poorly producing clones.
• isolation of variable domain-encoding nucleic acid fragments from rabbit-derived hybridomas is interfered by the endogenous light chain transcript of the commonly used myeloma fusion partner.
• the B-cell is a human B-cell, or a mouse B-cell, or a rat B-cell, or a rabbit B-cell, or a hamster B-cell, or a B-cell derived from a transgenic animal.
• the B-cell is a rabbit B-cell, or a human B-cell, or a B-cell derived from a transgenic animal.
• a transgenic animal is an animal in which the endogenous Ig locus has been inactivated or removed and which comprises an active or functional human Ig locus.
• the B-cell is a B-cell of an immunized experimental animal.
• the B-cell is a B-cell of an immunized human individual, or a human individual that has survived a disease, or a human that is suffering from a chronic disease.
• the B-cell is a single deposited antibody secreting B-cell.
• the B-cell is cultivated for 6 to 8 generations.
• the B-cell is cultivated until about 10 to about 100 cells are obtained.
• the B-cell produces about 10 ng/ml antibody after 7 days of cultivation. In one embodiment the B-cell produces about 20 ng/ml antibody after 7 days of cultivation.
• nucleic acid fragments encoding the variable domains are isolated and/or amplified by RT-PCR.
• nucleic acid fragment encoding the variable light chain domain and the nucleic acid fragment encoding the variable heavy chain domain are cognate nucleic acids. In one embodiment the nucleic acid fragments encoding the heavy and light chain variable domains are isolated from the same cell and/or their progeny.
• the B-cell is a rabbit B-cell and the nucleic acid encoding the variable heavy chain domain is isolated with the primer of SEQ ID NO: 5 (AAGCTTGCCACCATGGAGACTGGGCTGCGCTGGCTTC) and SEQ ID NO: 6 (CCATTGGTGAGGGTGCCCGAG).
• the B-cell is a rabbit B-cell and the nucleic acid encoding the variable light chain domain is isolated with the primer of SEQ ID NO: 7 (AAGCTTGCCACCATGGACAYGAGGGCCCCCACTC) and SEQ ID NO: 8 (CAGAGTRCTGCTGAGGTTGTAGGTAC).
• primer for amplification of e.g. rat, mouse or human immunoglobulin V-domain gene segments can be designed.
• the primer are directed to sequences in the first framework region. See e.g. van Dongen, J. J. M., et al. Leukemia 17 (2003) 2257; Widhopf, G. F., et al. Blood 111 (2008) 3137; Fais, F., et al. J. Clin. Invest. 102 (1998) 1515 for human B-cells; see e.g. Wang, Z., et al. J. Immunol. Methods. 233 (2000) 167; Jones, T. and Bendig, M., Bio/Technology 90 (1991) 88 for murine B-cells.
• the amplified nucleic acid is used without purification after removal of the PCR primer.
• the amplified nucleic acid is used without purification after removal of all PCR primer.
• nucleic acid fragments encoding the variable domains are inserted by sequence and ligation independent cloning (SLIC) into the eukaryotic expression plasmid.
• SLIC sequence and ligation independent cloning
• the insertion does not require restriction enzyme cleavage sites.
• the insertion does not require a phosphatase treatment of the nucleic acid fragment.
• the integration does not require an enzymatic ligation.
• the T4 DNA polymerase is employed in the absence of nucleotides for generating single strand extensions.
• the ratio of plasmid to nucleic acid is about 1:2 (w/w). In one embodiment about 100 ng plasmid and about 200 ng nucleic acid are used in the insertion step.
• the method is a high throughput method.
• the method is performed in parallel for at least ten B-cell clones.
• the efficiency of the method starting from the amplification product to the recombinantly expressed antibody is more than 50%.
• the nucleic acid is a pool of nucleic acids obtained from a pool of E. coli cells containing the assembled and/or amplified antibody expression plasmids for the antibody light and heavy chain, respectively.
• the plasmid from which the vector (or plasmid) backbone is amplified is linearized prior to the amplification. In one embodiment the plasmid is linearized by the use of two or more different restriction enzymes prior to the amplification.
• the amplification product is digested with a methylation dependent restriction enzyme, e.g. DpnI.
• a methylation dependent restriction enzyme e.g. DpnI.
• the light chain encoding plasmid backbone DNA is amplified with the primer of SEQ ID NO: 9 (GTACCTACAACCTCAGCAGCACTCTG) and SEQ ID NO: 10 (CCCTCRTGTCCATGGTGGCAAGCTTCCTCTGTGTTCAGTGCT G).
• the heavy chain encoding plasmid backbone DNA is amplified with the primer of SEQ ID NO: 11 (TGGGAACTCGGGCACCCTCACCAATGG) and SEQ ID NO: 12 (GCCCAGTCTCCATGGTGGCAAGCTTCCTCTGTGTTCAGT GCTG).
• cDNA was generated by reverse transcription of mRNA using the Super Script III first-strand synthesis SuperMix (Invitrogen) according to the manufacturer's instructions.
• a first step 6 ⁇ l of the isolated mRNA was mixed with 1 ⁇ l annealing buffer and 1 ⁇ l (50 ⁇ M) oligo dT, incubated for 5 minutes at 65° C. and thereafter immediately placed on ice for about 1 minute. Subsequently while still on ice 10 ⁇ l 2 ⁇ First-Strand Reaction Mix and SuperScriptTM III/RNaseOUTTM Enzyme Mix were added. After mixing the reaction was incubated for 50 minutes at 50° C. The reaction was terminated by incubation at 85° C. for 5 minutes. After termination the reaction mix was placed on ice.
• the polymerase chain reaction was carried out using AccuPrime Pfx SuperMix (Invitrogen) according to the manufacturer's instructions. Light chain and heavy chain variable regions were amplified in separate reactions. PCR-primer (0.2 ⁇ M/reaction) with 25 bp overlaps to target antibody expression vectors were used. After the PCR 8 ⁇ l of the PCR reaction mixture were used for analysis on 48-well eGels (Invitrogen).
• Residual PCR primer were removed using the NucleoSpin® 96 Extract II kit (Machery & Nagel) according to the manufacturer's instructions.
• the DNA sequences encoding the variable domains of the antibody heavy and light chains were obtained by sequencing the PCR products.
• the plasmid DNA to be used as recipient for the cloning of the PCR products encoding the antibody heavy and light chain variable domains was first linearized by restriction enzyme digestion. Subsequently, the linearized plasmid DNA was purified by preparative agarose electrophoresis and extracted from the gel (QIAquick Gel Extraction Kit/Qiagen). This purified plasmid DNA was added to a PCR-protocol as template using primer overlapping (by 20-25 bp) with the PCR-products to be cloned. The PCR was carried out using AccuPrime Pfx SuperMix (Invitrogen).
• PCR-products were cloned into expression vectors using a “site and ligation independent cloning” method (SLIC) which was described by Haun, R. S., et al. (BioTechniques 13 (1992) 515-518) and Li, M. Z., et al. (Nature Methods 4 (2007) 251-256). Both purified vector and insert were treated with 0.5 U T4 DNA polymerase (Roche Applied Sciences, Mannheim, Germany) per 1 ⁇ g DNA for 45 minutes at 25° C. in the absence of dNTPs to generate matching overhangs. The reaction was stopped by adding 1/10 th of the reaction volume of a 10 mM dCTP Solution (Invitrogen).
• SLIC site and ligation independent cloning
• the T4 treated vector and insert DNA fragments were combined with a plasmid:insert ratio of 1:2 (w/w) (e.g. 100 ng:200 ng) and recombined by adding RecAProtein (New England Biolabs) and 10 ⁇ RecA Buffer for 30 minutes at 37° C. Subsequently, 5 ⁇ l of each of the generated heavy chain and light chain expression plasmid was used to transform MultiShot Strip Well TOP 10 Chemically Competent E. coli cells (Invitrogen) using a standard chemical transformation protocol. After regeneration (shaking for 45 minutes at 37° C. of the transformed E.
• the entire transformation mixture was transferred into DWP 96 (deep well plates) containing 2 ml of LB medium supplemented with ampicillin per well. The cells were incubated in a shaker for 20 hours at 37° C.
• the plasmid DNA encoding the immunoglobulin heavy- and light chains was purified using the NucleoSpin 96 Plasmid Mini Kit (Macherey&Nagel), digested with selected restriction enzymes, and analyzed on 48-well eGels (Invitrogen). In parallel, glycerol stocks were prepared for storage.
• HEK293 cells were grown with shaking at 120 rpm in F17-medium (Gibco) at 37° C. in an atmosphere containing 8% CO 2 . Cells were split the day before transfection and seeded at a density of 0.7-0.8 ⁇ 10 6 cells/ml. On the day of transfection, 1-1.5 ⁇ 10 6 HEK293 cells in a volume of 2 ml were transfected with 0.5 ⁇ g HC plasmid plus 0.5 ⁇ g LC plasmid, suspended in 1 ⁇ l 293-free medium (Novagen) and 80 ⁇ l OptiMEM® medium (Gibco) in 48 well deep well plates. Cultures were incubated for 7 days at 180 rpm at 37° C. and 8% CO 2 . After 7 days the culture supernatants were harvested, filtered and analyzed for antibody content and specificity.
• B-cells to be used in the method as reported herein have to be selected based on the expression yield (antibody titer) obtained by the cultivation of the single deposited B-cell in the presence of feeder cells, e.g. EL4-B5 cells and Zubler mix.
• the obtained expression yield has to be above a specific threshold value as can be seen from the following Table 2.
• LC-primer rb-V-kappa-HindIIIs (SEQ ID NO: 13): GATTAAGCTTATGGACAYGAGGGCCCCCACTC rb-C-kappa-NheIas(SEQ ID NO: 14): GATCGCTAGCCCTGGCAGGCGTCTCRCTCTAACAG HC-primer rb-CH1rev-1(SEQ ID NO: 15): GCAGGGGGCCAGTGGGAAGACTG rbVH3-23for3(SEQ ID NO: 16): CACCATGGAGACTGGGCTGCGCTGGCTTC
• LC-primer rb-V-kappa-Slic-s001 (SEQ ID NO: 18): AAGCTTGCCACCATGGACAYGAGGGCCCCCACTC rbCk1-rev2(SEQ ID NO: 19): CAGAGTRCTGCTGAGGTTGTAGGTAC HC-primer rb-VH3-23-Slic-s001(SEQ ID NO: 20): AAGCTTGCCACCATGGAGACTGGGCTGCGCTGGCTTC rb-CH1rev-2(SEQ ID NO: 21): CCATTGGTGAGGGTGCCCGAG
• 8001-Slic-s001 (SEQ ID NO: 22): TGGGAACTCGGGCACCCTCACCAATGG 8001-Slic-as002(SEQ ID NO: 23): GCCCAGTCTCCATGGTGGCAAGCTTCCTCTGTGTTCAGTGCTG
• huIg-PCR-vectorprimer-as kappa (SEQ ID NO: 48): GGAATGCACACCTGTAGCTGTTGCTA huIg-PCR-vectorprimer-VK-s(SEQ ID NO: 49): GAGCTTCAACAGGGGAGAGTGT
• huIg-PCR-vectorprimer-as lambda (SEQ ID NO: 50): GGAATGCACACCTGTAGCTGTTGCTA huIg-PCR-vectorprimer-VL-s(SEQ ID NO: 51): GAAGGGAGCACCGTGGAGA
• Antibody variable region gene segments were amplified and cloned into the respective expression vectors as described in Example 1. To determine the fidelity of sequences derived from pool-cloning versus conventional clone-picking from single colonies, the transformation mix was split in two halves; one half was plated conventionally to generate single colonies while the other half was grown directly as pool-culture. Subsequently, plasmid was prepared both the pool-transformed E. coli cells as well as from single colonies picked from the conventional plates and the sequences of the cloned variable region gene segments was determined. As shown in the following Table 3, between 80% and 100% of colony-derived plasmids contained a correct variable region gene segment which was identical to the sequence obtained from the pool-transformation.
• VH and VL encoding nucleic acid sequence obtained from the sequencing of the pool cultivated cells were identical to the most abundant sequence obtained from the sequencing of individual clones.

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