Patent Application
20150376603
The present invention relates to a method for engineering and manufacturing of a molecule comprising a modified immunoglobulin variable domain polypeptide. The general field is the engineering of proteins with the aim to impart them with specific binding properties. More specifically, the engineered proteins of relevance here are immunoglobulins (antibodies), and even more specifically, single variable domains or pairs or combinations of single variable domains of immunoglobulins or combinations with other immunoglobulin domain˜. The specific binding properties of immunoglobulins are important features since they control the interaction with other molecules such as antigens, and render immunoglobulins useful for diagnostic and therapeutic applications.
The basic structure of antibodies is similar for various classes of antibodies and for various species and will be explained here using as example an intact IgG1 immunoglobulin. Two identical heavy (H) and two identical light (L) chains combine to form the Y-shaped antibody molecule. The heavy chains each have four domains. The amino terminal variable domains (VH) are at the tips of the Y. These are followed by three constant domains: CHI, CH2, and the carboxy-terminal CH3, at the base of the Y's stem. A short stretch, the switch, connects the heavy chain variable and constant regions. The hinge connects CH2 and CH3 (the Fe fragment) to the remainder of the antibody (the Fab fragments). One Fe and two identical Fab fragments can be produced by proteolytic cleavage of the hinge in an intact antibody molecule. The light chains are constructed of two domains, variable (VL) and constant (CL), separated by a switch.
Disulfide bonds in the hinge region connect the two heavy chains. The light chains are coupled to the heavy chains by additional disulfide bonds.
The variable regions of both the heavy and light chains (VH) and (VL) lie at the “tips” of the Y, where they are positioned to react with antigen. This tip of the molecule is the side on which the N-termini of the amino acid sequences are located.
The stem of the Y projects in a way to efficiently mediate effector functions such as the activation of complement and interaction with Fc receptors, or ADCC and ADCP. Its CH2 and CH3 domains bulge to facilitate interaction with effector proteins. The C-terminus of the amino acid sequence is located on the opposite side of the tip, which can be termed “bottom” of the Y.
Each domain in an antibody molecule has a similar structure of two beta sheets packed tightly against each other in a compressed antiparallel beta barrel. This conserved structure is termed the immunoglobulin fold. For reference see Bork et al. (1994) J. Mol. Biol. 242:309-320; Halaby et al. (1999) Protein Engineering 12: 563-571; Immunobiology. 5th ed. Janeway, Charles A.; Travers, Paul; Walport, Mark; Shlomchik, Mark. New York and London: Garland Publishing; 2001.
The fold of variable domains has 9 beta strands arranged in two sheets of 4 and 5 strands. The 5-stranded sheet is structurally homologous to the 3-stranded sheet of constant domains, but contains the extra strands C′ and C″. The remainder of the strands (A, B, C, D, E, F, G) have the same topology and similar structure as their counterparts in constant domain immunoglobulin folds. A disulfide bond links strands B and F in opposite sheets, as in constant domains. The variable domains of both light and heavy immunoglobulin chains contain three hypervariable loops, or complementarity-determining regions (CDRs). The three CDRs of a V domain (CDR1, CDR2, CDR3) cluster at one end of the beta barrel. The CDRs are loops that connect beta strands B-C, C′-C″, and F-G of the immunoglobulin fold. The residues in the CDRs vary from one immunoglobulin molecule to the next, imparting antigen specificity to each antibody.
The VL and VH domains at the tips of antibody molecules are closely packed such that the 6 CDRs (3 on each domain) cooperate in constructing a surface (or cavity) for antigen-specific binding. The natural antigen binding site of an antibody thus is composed of the loops which connect strands B-C, C′-C″, and F-G of the light chain variable domain and strands B-C, C′-C″, and F-G of the heavy chain variable domain.
Using the 3D structure of a protein as an aid for design, amino acid residues located on the surface of many proteins have been randomized using the core structure of the protein as scaffold. Examples for this strategy are described or reviewed in the following references and incorporated herein by reference: Nygren P A, Uhlen M., Curr Opin Struct Biol. (1997) 7:463-9; Binz H K, Amstutz P, Kohl A, Stumpp M T, Briand C, Forrer P, Grutter M G, Pluckthun A. Nat Biotechnol. (2004) 22:575-82; Vogt M, Skerra A. Chembiochem. (2004) 5:191-9; U.S. Pat. No. 6,562,617; Hufton et al. FEBS Letters (2000) 475: 225; Binz et al. Nat Biotechnol. (2005) 23:1257-68; Hosse et al. Protein Sci. (2006) 15:14-27.
The basic principle of this technique is based on the observation that many proteins have a stable core, formed by specific arrangements of secondary structure elements such as beta sheets or alpha helices, which are interconnected by structures such as loops, turns, or random coils. Typically, these latter three structure elements are less crucial for the overall structure of the protein, and amino acid residues in these structure elements can be exchanged often without destroying the general fold of the protein. Naturally occurring examples for this design principle are the CDRs of immunoglobulin-like domains as can be found in antibodies, T-cell receptors and other molecules of the immunoglobulin superfamily. Artificial examples include lipocalins, ankyrins, kunitz domain inhibitor, knottin and other protein scaffolds.
A multitude of prior art documents show that the immunoglobulin like scaffold has been employed for the purpose of manipulating the existing antigen- or ligand-binding site, thereby introducing novel binding properties. More precisely, mainly the CDR regions have been engineered for antigen binding, in other words, in the case of the immunoglobulin fold, the natural antigen binding site has been modified in order to change its binding affinity or specificity. A vast body of literature exist which describes different formats of such manipulated immunoglobulins, frequently expressed in the form of complete antibodies, fusion products and/or fragments such as single-chain Fv fragments (scFv), diabodies, minibodies, single domains or Fab fragments and the like, either displayed on the surface of phage particles or other viruses and cells or solubly expressed in various prokaryotic or eukaryotic expression systems. The techniques are reviewed e.g. in Holliger & Hudson, Nat. Biotechnol. (2005) 23:1126-36 and Hoogenboom, Nat. Biotechnol. (2005) 23:1105-16.
The CDR-loops of an immunoglobulin variable domain define the antigen specificity. The rest of the molecule is termed framework (FR). These framework regions however are composed of beta-strand and loop structures.
The loops which are not CDR-loops in a native immunoglobulin variable domain do not have antigen-binding or epitope-binding specificity but contribute to the correct overall folding of the immunoglobulin domain and consequently also to the correct positioning of the CDRs and to interaction between domains. These loops are named structural loops for the purpose of this invention.
Antibody variable domains in general have been manipulated for very many different reasons, such as the construction of various antibody formats, CDR grafting (i.e. grafting of specificity of a particular antibody into another framework; e.g. Jones et al. Nature (1986) 321: 522-525; Kashmiri et al. Methods (2005) 36:25-34), changing the surface of variable domains in order to make it more soluble and stable (e.g. Ewert et al. Methods (2004) 34:184-99; Conrath et al. J Mol Biol. (2005) 350:112-125), to render it monomeric (e.g. Dottorini et al. Biochemistry (2004) 43:622-628)) or to study the interaction between variable domains (e.g. Masuda et al. FEBS J. (2006) 273:2184-94). Many of those manipulations have involved changes in the framework region of the molecule; some amino acid mutations within structural loops of the variable domain have been performed.
The influence of remote framework regions on CDR-loop positioning is evident from CDR grafting results which show that mutation of framework amino acids frequently is necessary to regain antigen binding after grafting of CDRs from one framework to another (e.g. Foote & Winter (1992) J. Mol. Biol. 224: 487-499; Kettleborough et al. Protein Eng. (1991) 4:773-783; Wu et al. J. Mol. Biol. (1999) 294:151-162).
Simon & Rajwesky (Protein Sci. (1992) 5:229-234) have studied the effects of a four residue insertion into the FR3 loop of the heavy chain variable region from the anti-NP antibody B1-8. The insertion mutant was obtained as secreted antibody without major defects in biosynthesis, indicating that antibody variable domains can accommodate length variation not only in complementarity determining regions (CDRs), but also in framework region (FR) loops. In this case the original antigen binding site formed by the CDR-loops was not affected by the modification in a neighbouring structural loop.
Grafting of CDR-Loops into Structural Loop Regions
EP0640130B1 describes chimeric immunoglobulin superfamily protein analogues (chi-proteins) having more than one biological binding site (single V domains or Fvs). The binding sites on these proteins are comprised of hypervariable regions derived from molecules related to the immunoglobulin superfamily of molecules, including immunoglobulins, cell surface antigens (such as T-cell antigens) and cell receptors (such as Fc-receptor). The hypervariable regions are called “CDR-like regions” and define ligand binding sites. Additionally, the chi-protein has at least one more ligand binding site segment, also a CDR-like region, spliced into the FR-like regions of the beta-barrel domain.
Each ligand binding site of the chi-protein therefore is comprised of a CDR-like region derived from molecules of the immunoglobulin superfamily. For example, a ligand binding site is comprised of the CDRs derived from an immunoglobulin molecule whose ligand is an antigen.
EP0640130B1 thus teaches how to splice CDR-like regions with a given specificity from a molecule of the immunoglobulin superfamily into the structural loops of a variable domain.
It is postulated that functional bispecific antibodies can be prepared by this technique. There is a requirement for this technique that the relative orientations of the CDR-like loops (CDR loop symmetry) for a variable domain be reproduced to a reasonable approximation in the relative orientation of the structural loops. EP0640130B1 claims that such an approximation of the CDR-like loop symmetry does exist for the structural loops. However, it is doubtful that the relative orientation of the CDR-loops and the structural loops is similar in sufficient detail and resolution; consequently it has not been described to date that it is actually possible to develop bispecific molecules by this technique.
EP0640130B1 exemplifies that R19.9 (a monoclonal murine antibody specific for the p-azobenzenearsonate) and 26-10 (monoclonal murine antibody specific for ouabain) were used as the framework providing the primary CDR loops respectively, and the CDR-loops of murine anti-lysozyme antibody D1.3 were grafted into the structural loop regions. However, functional specificity after grafting is not described.
Another example describes that the single chain antibody 26-10 specific for ouabain could retain its ouabain-specificity after grafting two CDRs from the lysozyme-specific antibody into the structural loops of the ouabain-specific single-chain Fv antibody fragment. However, it is not described that the antibody fragment which was made according to this method had also lysozyme-binding specificity.
Grafting of Peptides into the Structural Loop Region
WO00244215A2 describes binding molecules comprising a specific target binding site and an Fc effector peptide. The Fc effector peptide is a peptide of up to 100 amino acids which interacts with effector molecules. The effector peptide may, e.g. be inserted into the loop regions of an antibody provided that the ability to bind an antigen is not adversely affected. The insertion of an effector peptide into a non-CDR loop of a CH1-domain of an immunoglobulin fragment is exemplified. The same insertion is not described for a variable domain.
Every peptide grafted into a non-CDR loop according to this disclosure has a high chance of being inactive due to the different structural environment in which it has been placed. In addition, it may be difficult to retain a specific CDR-loop conformation in a parent immunoglobulin if a peptide is grafted into a structural loop of a variable domain. Consequently, it is not described that an effector peptide can be grafted into a variable domain without loss of either antigen binding or effector molecule binding.
PCT/EP2006/050059 describes a method of engineering an immunoglobulin which comprises a modification in a structural loop region to obtain a new antigen binding sites. This method is broadly applicable to immunoglobulins and may be used to produce a series of immunoglobulins targeting a variety of antigens.
US2005/266000A1 describes polypeptides comprising a variant heavy chain variable framework domain (VFR). A VFR is part of the antigen binding pocket or groove that may contact antigen. VFRs are part of the CDR loop region, herein also called CDR region, and located at a variable domain at the side of the CDR loops to support the antigen binding via the CDR loop region. Framework loops other than VFR have not been mutated for the purpose of engineering an antigen binding site.
It is an object of the present invention to provide immunoglobulins and variable immunoglobulin domains with improved antigen binding properties and methods for engineering and manufacturing immunoglobulins with the improved variable domains.
The object is met by the subject matter of the present invention.
The present invention relates to a method for engineering an immunoglobulin comprising a variable domain and at least one modification in at least two structural loops of said immunoglobulin and determining the binding of said immunoglobulin to an epitope of an antigen, wherein the unmodified immunoglobulin does not significantly bind to said epitope, comprising the steps of:
The structural loops engineered according to the invention are preferably located within one or two structural loop regions, in some cases the modifications are placed in even more than 2 structural loop regions.
In order to overcome the shortcomings of the state of the art as described in WO00244215A2 and EP0640130B1 in engineering a binding site into a structural loop region of an antibody variable domain, the present invention provides methods to select specific binding of a polypeptide (i.e. a variable domain peptide comprising modified structural loop regions) in its natural context (i.e. antibody variable domain). In order to increase the number of potential structures of variant immunoglobulin domains which can be selected for antigen-binding at least two structural loops or loop regions are modified according to the invention. Thus it is possible to introduce and select for many different modifications with minimal disturbance of the overall domain structure. Another advantage of modifying at least two loops or loop regions is the enlarged surface area potentially able to interact with a specific binding partner. The thus modified immunoglobulin variable domains are selected for specific functions or binding. The invention enables to engineer a modified immunoglobulin variable domain and a modified immunoglobulin binding with its modified structural loops or loop regions with high affinity binding and/or high specificity to a binding partner. The method allows selection of specific binding molecules with minimal modifications and without destruction of the overall structure of the variable immunoglobulin domain.
To overcome the difficulty to retain a specific CDR-loop conformation in a parent immunoglobulin a structural loop of a variable domain is modified according to the invention. It is thus the first time possible to add to the antigen binding properties of an immunoglobulin without significant loss of antigen binding or even effector molecule binding of a parent antibody. It is surprisingly possible to engineer the immunoglobulin according to the invention without significantly interfering with the binding properties of a specific CDR-loop conformation, such as binding affinity, avidity and specificity, of the parent immunoglobulin.
A specific CDR-loop conformation provides for antigen-binding by CDR loops or a CDR loop region. Any immunoglobulin that is antigen binding through such a CDR-loop conformation may be modified according to the invention to obtain an additional binding site in a structural loop of the immunoglobulin, preferably while the specific CDR-loop conformation and the original antigen binding properties of the parent molecule may be retained or unchanged. Preferably the binding properties of the CDR-loop conformation may be maintained to the extend that the binding affinity of the parent molecule is not significantly reduced, for instance, the dissociation constant Kd is not significantly increased, meaning that the difference in Kd is a factor preferably less than 104, more preferably less than 103, even more preferred less than 102, or less than 10.
In accordance with the present invention, one of the key features of the present invention is that the engineering of the immunoglobulin or immunoglobulin variable domains takes place in regions which are not normally involved in antigen binding, in other words, in regions other than the CDRs of an antibody variable domain. It was observed that the specific fold of immunoglobulin domains allows the introduction of random mutations in regions which are structurally analogous to the CDRs but different in position in sequence and structure. The regions identified for modification according to the present invention are, like CDRs, loop regions connecting the beta strands of the immunoglobulin fold. These structural loops or loop regions can be mutated as described in the present invention without affecting the binding of the variable domains of the immunoglobulin that is mediated through the CDR loops. By mutating said structural loops or loop regions, a new molecular binding surface or binding pocket is generated that is similar in size and shape to the binding surface or binding pocket formed by the CDR loops of the natural antigen binding site of an antibody. Since the structural loops can also be extended by the insertion of additional amino acids, the architecture of the newly generated binding site can be voluntarily adjusted to the target to which it should hind. For example, deep binding pockets which are especially suitable for the binding of small molecules can be preferentially formed by long loops, i.e. structural loops with additional amino acids inserted in their sequence, whereas rather flat binding surfaces, which are well suited to bind to targets with a large, flat molecular surface are preferentially formed when the residues in the structural loops are mutated without the insertion of additional residues More specifically, it is described herein that by introducing random mutations in the loops connecting beta strands A-B, C′-D and E-F of a human or humanized heavy chain variable domain, mutated domains can be selected that bind specifically to either human serum albumin or to Fcgamma receptor III, which are not normally recognized and bound by human or humanized immunoglobulin variable domains. The mutations introduced include mutations in which selected amino acid residues in the wild-type sequence were replaced by randomly chosen residues, and they also include insertions of extra amino acid residues in the loops mentioned above. Thus, preferably modified immunoglobulins are provided according to the invention that are obtainable and produced according to the above described methods, and have a binding site specific for an antigen, in particular specific for a serum albumin, cell receptors and complement factors, more specifically human serum albumin and Fc receptors.
In particular, the present invention relates to a method for engineering an immunoglobulin variable domain and an immunoglobulin containing such a domain that is binding specifically to an epitope of an antigen.
Specifically the method according to the invention comprises the steps of:
This method preferably applies to immunoglobulin variable domain peptides. More preferably the method according to this embodiment of the invention relates to immunoglobulins that bind to said first epitope through their CDR-regions or specific CDR-loop conformation.
The method according to the invention refers further to at least one modification in each of at least two structural loops or loop regions of said immunoglobulin variable domain and determining the specific binding of said structural loops or loop regions to at least one antigen, wherein the immunoglobulin variable domain containing an unmodified structural loop or loop region does not specifically bind to such an antigen.
The term “immunoglobulin” as used herein is including immunoglobulins or parts, fragments or derivatives of immunoglobulins. Thus it includes an “immunoglobulin variable domain peptide” to be modified according to the present invention (as used herein the terms immunoglobulin and antibody are interchangeable) as well as immunoglobulin variable domains or parts thereof that contain a structural loop, such as a minidomain, or a structural loop of such domains. The immunoglobulins can be used as isolated peptides or as combination molecules with other peptides. In some cases it is preferable to use a defined modified structural loop or a structural loop region, or parts thereof, as isolated molecules for binding or combination purposes. The “immunoglobulin variable domain” as defined herein contains such immunoglobulin variable domain peptides or polypeptides that may have specific binding characteristics upon modifying and engineering. The peptides are homologous to immunoglobulin variable domain sequences, and are preferably at least 5 amino acids long, more preferably at least 10 or even at least 50 or 100 amino acids long, and constitute at least partially the structural loop region or the non-CDR loop region of the variable domain. Preferably the peptides exclude those insertions that are considered non-functional amino acids, hybrid or chimeric CDR-regions or CDR-like regions and/or canonical structures of CDR regions. The binding characteristics relate to specific epitope binding, affinity and avidity.
A derivative of an immunoglobulin according to the invention is any combination of one or more immunoglobulins of the invention and or a fusion protein in which any domain or minidomain of the immunoglobulin of the invention may be fused at any position of one ore more other proteins (such as other immunoglobulins, ligands, scaffold proteins, enzymes, toxins and the like). A derivative of the immunoglobulin of the invention may also be obtained by recombination techniques or binding to other substances by various chemical techniques such as covalent coupling, electrostatic interaction, disulphide bonding etc.
The other substances bound to the immunoglobulins may be lipids, carbohydrates, nucleic acids, organic and anorganic molecules or any combination thereof (e.g. PEG, prodrugs or drugs). A derivative is also an immunoglobulin with the same amino acid sequence but made completely or partly from non-natural or chemically modified amino acids.
The engineered molecules according to the present invention will be useful as stand-alone proteins as well as fusion proteins or derivatives, most typically fused in such a way as to be part of larger antibody structures or complete antibody molecules, or parts thereof such as Fab fragments, Fc fragments, Fv fragments and others. It will be possible to use the engineered proteins to produce molecules which are bispecific, trispecific, and maybe even carry more specificities at the same time, and it will be possible at the same time to control and preselect the valency of binding at the same time according to the requirements of the planned use of such molecules.
Another aspect of the present invention relates to an immunoglobulin with at least one loop region besides the CDR-loop conformation of the variable domain, characterised in that said at least one loop region comprises at least one amino acid modification forming at least one modified loop region, wherein said at least one modified loop region binds specifically to at least one epitope of an antigen.
It is preferred to molecularly combine at least one modified antibody domain, which is binding to the specific partner via the non-variable sequences or a structural loop, with at least one other binding molecule, which can be an antibody, antibody fragment, a soluble receptor, a ligand or another modified antibody domain.
The molecule that functions as a part of a binding pair that is specifically recognized by the immunoglobulin according to the invention is preferably selected from the group consisting of proteinaceous molecules, nucleic, acids and carbohydrates.
The modified loops or loop regions of the immunoglobulins according to the invention may specifically bind to any kind of binding molecules or structures, in particular to antigens, proteinaceous molecules, proteins, peptides, polypeptides, nucleic acids, glycans, carbohydrates, lipids, small organic molecules, anorganic molecules, or combinations or fusions thereof. Of course, the modified immunoglobulins may comprise at least two loops or loop regions whereby each of the loops or loop regions may specifically bind to different molecules or epitopes.
According to the present invention, binding regions to antigens or antigen binding sites of all kinds of cell surface antigens, may be introduced into a structural loop of a given antibody structure.
Binding of the immunoglobulins according to the invention is preferably on the one hand through CDR-regions, if the immunoglobulin contains such a CDR-region, and on the other hand through an additional binding site that is formed by modifying at least two structural loops. Those structural loops are either placed on one or at least two variable domains having one or more modified structural loops. Thus, an immunoglobulin according to the invention contains at least two modifications in the structural loops of variable domains either through at least one modification of at least two variable domains or at least two modifications of at least one variable domain. Preferably the modified immunoglobulin thus exhibits a binding site either by changing the primary structure of the protein or by changing the tertiary structure to obtain a conformation specific binding site.
By analogy the immunoglobulin variable domains from any class of immunoglobulins and from immunoglobulins from any species are amenable to this type of engineering. Furthermore not only the specific loops targeted in the examples of the present invention can be manipulated, but any loop connecting beta strands in immunoglobulin variable domains can be manipulated in the same way.
Engineered immunoglobulins or, immunoglobulin variable domains from any organism and from any class of immunoglobulin can be used according to the present invention either as such (as single domains), or as part of a larger molecule. For example, they can be part of an intact immunoglobulin, which accordingly would have its “normal” antigen binding region formed by at least one of the 6 CDRs and the new, engineered antigen binding site. Like this, a multi-specific, e.g. bispecific, or trispecific immunoglobulin could be generated. The engineered immunoglobulin domains can also be part of any fusion protein.
Immunoglobulins or immunoglobulin variable domains according to the invention may be complete antibody molecules or part of antibodies, such as IgG, IgA, IgM, IgD, IgE and the like. The immunoglobulins or immunoglobulin variable domains of the invention may also contain or consist of a functional antibody fragment such as Fab, Fab2, scFv, Fv, or parts thereof, or other derivatives or combinations of the immunoglobulins such as minibodies, domains of the heavy and light chains of the variable region (such as Fd, VL, including Vlambda and Vkappa, VH, VHH) as well as mini-domains consisting of two beta-strands of an immunoglobulin domain connected by at least two structural loops (see for example Laffly et al (2005) Hum Antibodies. 2005; 14:33-55), as isolated domains or in the context of naturally associated molecules.
The modified immunoglobulin according to the invention is possibly further combined with one or more modified immunoglobulins or with unmodified immunoglobulins, or parts thereof, to obtain a combination immunoglobulin. Combinations are preferably obtained by recombination techniques, but also by association through adsorption, electrostatic interactions or the like, or else through chemical binding with or without a linker. The preferred linker sequence is either a natural linker sequence or a functionally suitable artificial sequence.
It is understood that the term “immunoglobulin”, “immunoglobulin variable domain peptide” and “immunoglobulin variable domain” includes derivatives as well. A derivative is any part or combination of one or more immunoglobulins and/or a fusion protein in which any domain or minidomain of the immunoglobulin as obtained according to the invention may be combined or fused at any position with one ore more other peptides or proteins (including but not limited to other immunoglobulins, immunoglobulin domains, Fc parts, ligands, scaffold proteins, enzymes, toxins, serum proteins and the like). A derivative of the immunoglobulin of the invention may also be obtained by binding the unmodified or modified immunoglobulin or immunoglobulin variable domain of the invention to other substances by various chemical techniques such as covalent coupling, electrostatic interaction, disulphide bonding etc.
The other substances bound to the immunoglobulin or immunoglobulin variable domain may be lipids, carbohydrates, nucleic acids, organic and anorganic molecules or any combination thereof (e.g. PEG, pro-drugs or drugs). A derivative is also an immunoglobulin or immunoglobulin variable domain with the same amino acid sequence but made completely or partly from non-natural, artificial or chemically modified amino acids.
The engineered molecules according to the present invention will be useful as stand-alone proteins as well as fusion proteins or derivatives, most typically fused before or after modification in such a way as to be part of larger antibody structures or complete antibody molecules, or parts thereof. Immunoglobulins according to the invention may thus also consist of or comprise Fab fragments, Fc fragments, Fv fragments, single chain antibodies, in particular single-chain Fv fragments, bi- or multispecific scFv, diabodies, multibodies, multivalent or multimers of immunoglobulin domains and others. It will be possible to use the engineered proteins to produce molecules which are monospecific, bispecific, trispecific, and molecules that may even carry more specificities. By the invention it is possible to control and preselect the valency of binding at the same time according to the requirements of the planned use of such molecules.
According to the present invention, one or more binding sites to antigens or antigen binding sites to one or more antigens may be introduced into a structural loop or loop region of a given antibody variable domain structure. The antigens may be naturally occurring molecules or chemically synthesized molecules or recombinant molecules, either in solution or in suspension, e.g. located on or in particles such as solid phases, on or in cells or on viral surfaces. It was surprising that the binding of an immunoglobulin to an antigen could be achieved according to the invention, even when the antigen is still adhered or bound to molecules and structures that would hinder its binding. By employing the target antigen in its selected or natural context and structure for selecting the modified and designed immunoglobulin, it is possible to identify and obtain those modified immunoglobulins that are best suitable for the purpose of diagnostic or therapeutic use.
The term “antigen” as used herein shall comprise molecules selected from the group consisting of allergens, tumor associated antigens, self antigens including albumin, T cell receptors, FcRn, cell surface receptors, enzymes, Fc-receptors, proteins of the complement system, serum molecules, bacterial antigens, fungal antigens, protozoan antigen and viral antigens, also molecules responsible for transmissible spongiform encephalitis (TSE), such as prions, infective or not, and markers or molecules that relate to Alzheimer disease. Antigens can be targeted and bound by the immunoglobulins or immunoglobulin variable domains as engineered according to the invention through at least part of a modified structural loop.
In a preferred embodiment the immunoglobulin is binding with its modified structural loops specifically to at least two such epitopes that are identical or differ from each other, either of the same antigen or of different antigens.
For example, the method according to the invention refers to engineering an immunoglobulin or immunoglobulin variable domain that is binding specifically to at least one first epitope and comprising at least one modification in each of at least two structural loops or loop regions of said immunoglobulin, and determining the specific binding of said loops or loop regions to at least one second epitope, the epitope being selected from the group of antigens as mentioned above, wherein the unmodified structural loop or loop region (non-CDR region) does not specifically bind to said at least one second epitope.
The term antigen as used according to the present invention shall in particular include all antigens and target molecules capable of being recognised by a binding site of an immunoglobulin or an antibody structure, as a whole target molecule or as a fragment of such molecule (especially substructures of targets, generally referred to as “epitopes”).
Preferred antigens as targeted by the immunoglobulins according to the invention are those antigens or molecules, which have already been proven to be or are capable of being immunogenic, bound by immune response factors, or else immunologically or therapeutically relevant, especially those, for which a clinical efficacy has been tested.
The term “antigen” according to the present invention shall mean molecules or structures known to interact or capable of interacting with the CDR-loop region of immunoglobulins. Structural loop regions of the prior art referring to native antibodies, do not interact with antigens but rather contribute to the overall structure and/or to the binding to effector molecules. Only upon engineering according to the invention structural loops may form antigen binding pockets without involvement of CDR loops or the CDR region.
According to a preferred embodiment the antigen bound by the immunoglobulin according to the invention is a cell surface antigen. The term “cell surface antigens” shall include all antigens or capable of being recognised by an antibody structure on the surface of a cell, and fragments of such molecules. Preferred “cell surface antigens” are those antigens, which have already been proven to be or which are capable of being immunologically or therapeutically relevant, especially those, for which a preclinical or clinical efficacy has been tested. Those cell surface molecules are specifically relevant for the purpose of the present invention, which mediate cell killing activity. Upon binding of the immunoglobulin according to the invention to at least two of those cell surface molecules the immune system provides for cytolysis or cell death, thus a potent means for attacking human cells may be provided.
Preferably the antigen is selected from cell surface antigens, including receptors, in particular from the group consisting of erbB receptor tyrosine kinases (such as EGFR, HER2, HER3 and HERO, but not limited to these), molecules of the TNF-receptor superfamily, such as Apo-1 receptor, TNFR1, TNFR2, nerve growth factor receptor NGFR, CD40, T-cell surface molecules, T-cell receptors, T-cell antigen OX40, TACI-receptor, BCMA, Apo-3, DR4, DR5, DR6, decoy receptors, such as DcR1, DcR2, CAR1, HVEM, GITR, ZTNFR-5, NTR-1, TNFL1 but not limited to these molecules, B-cell surface antigens, such as CD10, CD19, CD20, CD21, CD22, antigens or markers of solid tumors or hematologic cancer cells, cells of lymphoma or leukaemia, other blood cells including blood platelets, but not limited to these molecules.
According to a further preferred embodiment of the present invention the antigen or the molecule binding to the modified structural loop or loop region is selected from the group consisting of tumor associated antigens, in particular EpCAM, tumor-associated glycoprotein-72 (TAG-72), tumor-associated antigen CA 125, Prostate specific membrane antigen (PSMA), High molecular weight melanoma-associated antigen (HMW-MAA), tumor-associated antigen expressing Lewis Y related carbohydrate, Carcinoembryonic antigen (CEA), CEACAM5, HMFG PEM, mucin MUC1, MUC18 and cytokeratin tumor-associated antigen, bacterial antigens, viral antigens, allergens, allergy related molecules IgE, cKIT and Fc-epsilon-receptorI, IRp60, IL-5 receptor, CCR3, red blood cell receptor (CR1), human serum albumin, mouse serum albumin, rat serum albumin, neonatal Fc-gamma-receptor FcRn, Fc-gamma-receptors Fc-gamma RI, Fc-gamma-RII, Fc-gamma RIII, Fc-alpha-receptors, Fc-epsilon-receptors, fluorescein, lysozyme, toll-like receptor 9, erythropoietin, CD2, CD3, CD3E, CD4, CD11, CD11a, CD14, CD16, CD18, CD19, CD20, CD22, CD23, CD25, CD28, CD29, CD30, CD32, CD33 (p67 protein), CD38, CD40, CD40L, CD52, CD54, CD56, CD64, CD80, CD147, GD3, IL-1, IL-1R, IL-2, IL-2R, IL-4, IL-5, IL-6, IL-6R, IL-8, IL-12, IL-15, IL-18, IL-23, interferon alpha, interferon beta, interferon gamma; TNF-alpha, TNFbeta2, TNFalpha, TNFalphabeta, TNF-R1, TNF-RII, FasL, CD27L, CD30L, 4-1BBL, TRAIL, RANKL, TWEAK, APRIL, BAFF, LIGHT, VEG1, OX40L, TRAIL Receptor-1, A1 Adenosine Receptor, Lymphotoxin Beta Receptor, TACI, BAFF-R, EPO; LFA-3, ICAM-1, ICAM-3, integrin beta1, integrin beta2, integrin alpha4/beta7, integrin alpha2, integrin alpha3, integrin alpha4, integrin alpha5, integrin alpha6, integrin alphav, alphaVbeta3 integrin, FGFR-3, Keratinocyte Growth Factor, VLA-1, VLA-4, L-selectin, anti-Id, E-selectin, HLA, HLA-DR, CTLA-4, T cell receptor, B7-1, B7-2, VNRintegrin, TGFbeta1, TGFbeta2, ectaxin1, BLyS (B-lymphocyte Stimulator), complement C5, IgE, IgA, IgD, IgM, IgG, factor VII, CBL, NCA 90, EGFR (ErbB-1), Her2/neu (ErbB-2), Her3 (ErbB-3), Her4 (ErbB4), Tissue Factor, VEGF, VEGFR, endothelin receptor, VLA-4, carbohydrates such as blood group antigens and related carbohydrates, Galili-Glycosylation, Gastrin, Gastrin receptors, tumor associated carbohydrates, Hapten NP-cap or NIP-cap, T cell receptor alpha/beta, E-selectin, P-glycoprotein, MRP3, MRP5, glutathione-S-transferase pi (multi drug resistance proteins), alpha-granule membrane protein (GMP) 140, digoxin, placental alkaline phosphatase (PLAP) and testicular PLAP-like alkaline phosphatase, transferrin receptor, Heparanase I, human cardiac myosin, Glycoprotein IIb/IIIa (GPIIb/IIIa), human cytomegalovirus (HCMV) gH envelope glycoprotein, HIV gp120, HCMV, respiratory syncital virus RSV F, RSVF Fgp, VNRintegrin, Hep B gp120, CMV, gpIIbIIIa, HIV IIIB gp120 V3 loop, respiratory syncytial virus (RSV) Fgp, Herpes simplex virus (HSV) gD glycoprotein, HSV gB glycoprotein, HCMV gB envelope glycoprotein, Clostridium perfringens toxin and fragments thereof.
Preferably, the antigen is selected from the group consisting of pathogen antigen, tumor associated antigen, enzyme, substrate, self antigen, organic molecule or allergen. More preferred antigens are selected from the group consisting of viral antigens, bacterial antigens or antigens from pathogens of eukaryots or phages. Preferred viral antigens include HAV-, HBV-, HCV-, HIV I-, HIV II-, Parvovirus-, Influenza-, HSV-, Hepatitis Viruses, Flaviviruses, Westnile Virus, Ebola Virus, Pox-Virus, Smallpox Virus, Measles Virus, Herpes Virus, Adenovirus, Papilloma Virus, Polyoma Virus, Parvovirus, Rhinovirus, Coxsackie virus, Polio Virus, Echovirus, Japanese Encephalitis virus, Dengue Virus, Tick Borne Encephalitis Virus, Yellow Fever Virus, Coronavirus, respiratory syncytial virus, parainfluenza virus, La Crosse Virus, Lassa Virus, Rabies Viruse, Rotavirus antigens; preferred bacterial antigens include Pseudomonas-, Mycobacterium-, Staphylococcus-, Salmonella-, Meningococcal-, Borellia-, Listeria, Neisseria-, Clostridium-, Escherichia-, Legionella-, Bacillus-, Lactobacillus-, Streptococcus-, Enterococcus-, Corynebacterium-, Nocardia-, Rhodococcus-, Moraxella-, Brucella, Campylobacter-, Cardiobacterium-, Francisella-, Helicobacter-, Haemophilus-, Klebsiella-, Shigella-, Yersinia-, Vibrio-, Chlamydia-, Leptospira-, Rickettsia-, Mycobacterium-, Treponema-, Bartonella-antigens. Preferred eukaryotic antigens of pathogenic eukaryotes include antigens from Giardia, Toxoplasma, Cyclospora, Cryptosporidium, Trichinella, Yeasts, Candida, Aspergillus, Cryptococcus, Blastomyces, Histoplasma, Coccidioides.
The modified immunoglobulin according to the present invention may preferably bind to one of the molecules disclosed above. These molecules comprise also allergens and haptens.
Substructures of antigens are generally referred to as “epitopes” (e.g. B-cell epitopes, T-cell epitopes), as long as they are immunologically relevant, i.e. are also recognisable by natural or monoclonal antibodies. The term “epitope” according to the present invention shall mean a molecular structure which may completely make up a specific binding partner or be part of a specific binding partner to the binding domain or the immunoglobulin of the present invention.
Chemically, an epitope may either be composed of a carbohydrate, a peptide, a fatty acid, an anorganic substance or derivatives thereof and any combinations thereof. If an epitope is a peptide or polypeptide, there will usually be at least 3 amino acids, preferably 8 to 50 amino acids, and more preferably between about 10-20 amino acids included in the peptide. There is no critical upper limit to the length of the peptide, which could comprise nearly the full length of the polypeptide sequence. Epitopes can either be linear or conformational epitopes. A linear epitope is comprised of a single segment of a primary sequence of a polypeptide chain. Linear epitopes can be contiguous or overlapping. Conformational epitopes are comprised of amino acids brought together by folding of the polypeptide to form a tertiary structure and the amino acids are not necessarily adjacent to one another in the linear sequence.
Specifically, epitopes are at least part of diagnostically relevant molecules, i.e. the absence or presence of an epitope in a sample is qualitatively or quantitatively correlated to either a disease or to the health status or to a process status in manufacturing or to environmental and food status. Epitopes may also be at least part of therapeutically relevant molecules, i.e. molecules which can be targeted by the specific binding domain which changes the course of the disease.
Besides the antigen binding sites of the immunoglobulin as engineered according to the invention further binding capacities may be introduced aside from or into the structural loop regions of variable domains, e.g. binding capacities for other antigens, small molecules, for drugs or enzymes, catalytic sites of enzymes or enzyme substrates or the binding to a transition state analogue of an enzyme substrate.
Preferably the new antigen binding site in the structural loops is foreign to the unmodified immunoglobulin variable domain. Thus foreign targets like effector molecules, serum proteins or Fc-receptors or cell surface receptors, which are not bound by variable domains by nature, are preferred as antigens or binding molecules bound by the immunoglobulin variable domains according to the invention.
In this context the term “foreign” means that the antigen is not recognized by the specific CDR binding region or other natural or intrinsic binding regions of the immunoglobulin. A foreign binding partner, but not the natural binding partner of an immunoglobulin, may thus be bound by the newly formed antigen binding site of a structural loop. This means that a natural binding partner, such as an Fc-receptor or an effector of the immune system, is not considered to be bound by the antigen binding site foreign to the unmodified immunoglobulin.
As used herein, the term “specifically binds” or “specific binding” refers to a binding reaction, which is determinative of the cognate ligand of interest in a heterogeneous population of molecules. Thus, under designated conditions (e.g. immunoassay conditions), the specified antibody variable domain binds to its particular “target” and does not bind in a significant amount to other molecules present in a sample. The specific binding means that binding is selective in terms of target identity, high, medium or low binding affinity or avidity, as selected. Selective binding is usually achieved if the binding constant or binding dynamics is at least 10 fold different.
The term “expression system” refers to nucleic acid molecules containing a desired coding sequence and control sequences in operable linkage, so that hosts transformed or transfected with these sequences are capable of producing the encoded proteins. In order to effect transformation, the expression system may be included on a vector; however, the relevant DNA may then also be integrated into the host chromosome. Alternatively, an expression system can be used for in vitro transcription/translation.
A “structural loop” or “non-CDR-loop” according to the present invention is to be understood in the following manner: immunoglobulins are made of domains with a so called immunoglobulin fold. In essence, anti-parallel beta sheets are connected by loops to form a compressed antiparallel beta barrel. In the variable region, some of the loops of the domains contribute essentially to the specificity of the antibody, i.e. the binding to an antigen. These loops are called CDR-loops.
The CDR loops are located within the CDR loop region, which may in some cases also the variable framework region (called “VFR”) adjacent to the CDR loops. It is known that VFRs may contribute to the antigen binding pocket of an antibody, which generally is mainly determined by the CDR loops. Thus, those VFRs are considered as part of the CDR loop region, and would not be appropriately used for the purpose of the invention. Contrary to those VFRs within the CDR loop region or located proximal to the CDR loops, other VFRs of variable domains would be particularly suitable to be used according to the invention. Those are the structural loops of the VFRs located opposite to the CDR loop region, or at the C-terminal side of a variable immunoglobulin domain.
All loops of antibody variable domains outside the CDR loop region are rather contributing to the structure of the molecule. These loops are defined herein as structural loops or non-CDR-loops.
All numbering of the amino acid sequences of the immunoglobulins is according to the IMGT numbering scheme (IMGT, the international ImMunoGeneTics information system@imgt.cines.fr; http://imgt.cines.fr; Lefranc et al., 1999, Nucleic Acids Res. 27: 209-212; Ruiz et al., 2000 Nucleic Acids Res. 28: 219-221; Lefranc et al., 2001, Nucleic Acids Res. 29: 207-209; Lefranc et al., 2003, Nucleic Acids Res. 31: 307-310; Lefranc et al., 2005, Dev Comp Immunol 29:185-203).
According to a preferred embodiment of the present invention the immunoglobulin variable domain is of human, camelid, rabbit; chicken, rat, dog, horse, sheep or murine origin.
Since the modified immunoglobulin may be employed for various purposes, in particular in pharmaceutical compositions, the immunoglobulin is preferably of human, camelid or murine origin.
Of course, the modified immunoglobulin may also be a humanized or a chimeric immunoglobulin. In the most preferred embodiment of the invention the modified variable domain is of human origin or a humanized version of a variable domain of any species.
A humanized immunoglobulin variable domain has at least about 50% amino acid sequence identity, preferably at least about 55% amino acid sequence identity, more preferably at least about 60% amino acid sequence identity, more preferably at least about 65% amino acid sequence identity, more preferably at least about 70% amino acid sequence identity, more preferably at least about 75% amino acid sequence identity, more preferably at least about 80% amino acid sequence identity, more preferably at least about 85% amino acid sequence identity, more preferably at least about 90% amino acid sequence identity, more preferably at least about 95% amino acid sequence identity to a native human immunoglobulin variable domain sequence.
A humanized immunoglobulin variable domain has furthermore at least about 50% amino acid sequence identity, preferably at least about 55% amino acid sequence identity, more preferably at least about 60% amino acid sequence identity, more preferably at least about 65% amino acid sequence identity, more preferably at least about 70% amino acid sequence identity, more preferably at least about 75% amino acid sequence identity, more preferably at least about 80% amino acid sequence identity, more preferably at least about 85% amino acid sequence identity, more preferably at least about 90% amino acid sequence identity, more preferably at least about 95% amino acid sequence identity when comparing all surface accessible amino acids to the surface accessible amino acids of a native human immunoglobulin variable domain sequence.
The preferred homology or sequence identities specifically relates to those sequences of the framework region.
The preferred immunoglobulin according to the invention comprises a domain that has at least 50% homology with the unmodified domain.
The term “homology” indicates that polypeptides have the same or conserved residues at a corresponding position in their primary, secondary or tertiary structure. The term also extends to two or more nucleotide sequences encoding the homologous polypeptides.
“Homologous immunoglobulin domain” means an immunoglobulin domain according to the invention having at least about 50% amino acid sequence identity with regard to a full-length native sequence immunoglobulin domain sequence or any other fragment of a full-length immunoglobulin domain sequence as disclosed herein. Preferably, a homologous immunoglobulin domain will have at least about 50% amino acid sequence identity, preferably at least about 55% amino acid sequence identity, more preferably at least about 60% amino acid sequence identity, more preferably at least about 65% amino acid sequence identity, more preferably at least about 70% amino acid sequence identity, more preferably at least about 75% amino acid sequence identity, more: preferably at least about 80% amino acid sequence identity, more preferably at least about 85% amino acid sequence identity, more preferably at least about 90% amino acid sequence identity, more preferably at least about 95% amino acid sequence identity to a native immunoglobulin domain sequence, or any other specifically defined fragment of a full-length immunoglobulin domain sequence as disclosed herein.
“Percent (%) amino acid sequence identity” with respect to the immunoglobulin domain sequences identified herein is defined as the percentage of amino acid residues in a candidate sequence that are identical with the amino acid residues in the specific immunoglobulin variable domain sequence, after aligning the sequence 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 measuring alignment, including any algorithms needed to achieve maximal alignment over the full length of the sequences being compared.
% amino acid sequence identity values may be obtained as described below by using the WU-BLAST-2 computer program (Altschul et al., Methods in Enzymology 266:460-480 (1996)). Most of the WU-BLAST-2 search parameters are set to the default values. Those not set to default values, i.e., the adjustable parameters, are set with the following values: overlap span=1, overlap fraction=0.125, word threshold (T)=11, and scoring matrix=BLOSUM62. When WU-BLAST-2 is employed, a % amino acid sequence identity value is determined by dividing (a) the number of matching identical amino acid residues between the amino acid sequence of the immunoglobulin variable domain of interest having a sequence derived from the native immunoglobulin variable domain and the comparison amino acid sequence of interest (i.e., the sequence against which, the immunoglobulin variable domain of interest is being compared which may be the unmodified immunoglobulin variable domain) as determined by WU-BLAST-2 by (b) the total number of amino acid residues of the non-randomized parts of the immunoglobulin variable domain of interest. For example, in the statement “a polypeptide comprising an amino acid sequence X which has or having at least 80% amino acid sequence identity to the amino acid sequence Y”, the amino acid sequence A is the comparison amino acid sequence of interest and the amino acid sequence B is the amino acid sequence of the immunoglobulin variable domain of interest.
In a preferred embodiment the polypeptide according to the invention is a bispecific antibody or a bispecific single chain antibody or a bispecific Fab or a bispecific sdAb. Further preferred is that the polypeptide comprises a bispecific domain or a part thereof. Specific examples refer to Fab or dAb molecules with additional functionality through the new binding site at the opposite side of the CDR region. The preferred immunoglobulin according to the invention, which is a Fab molecule, may, for example, contain one or two additional binding sites at the C-terminal loop side of a CH1 and/or a CL domain. The preferred immunoglobulin according to the invention, which is a dAb molecule, may, for example, contain an additional binding site at the C-terminal loop side of a Vh, Vhh or Vl domain. By such additional binding sites additional functionalities, like prolonged half life (e.g. through binding to an FcRn or serum proteins, such as albumin or IgG), or effector function (e.g. through binding to T cell receptors, C1q or CD64) can be added to the molecules. According to such examples the dedicated Fab or dAb libraries, would be prepared with an appropriate size to enable selection of the specific binders to the specific binding partners.
The preferred variable domain according to the invention is selected from the group of VH, VL, including Vkappa and Vlambda, VHH and combinations thereof. It turned out that those modifications are of specific advantage when brought into the loops or loop regions of a VH, a Vkappa, a Vlambda or a VHH, and the modified loops or loop regions comprise at least one modification within amino acids 7 to 21, amino acids 25 to 39, amino acids 41 to 81, amino acids 83 to 85, amino acids 89 to 103 or amino acids 106 to 117.
The structural loops or loop regions of the immunoglobulin or variable domain of the immunoglobulin of human or humanized origin as modified according to the invention are selected preferably from the structural loops that comprise amino acids 8 to 20, amino acids 44 to 50, amino acids 67 to 76 and amino acids 89 to 101, most preferably amino acid positions 12 to 17, amino acid positions 45 to 50, amino acid positions 69 to 75 and amino acid positions 93 to 98.
In another preferred embodiment a modification in the structural loops or loop regions comprising amino acids 93 to 98 is combined with a modification in the structural loops or loop regions comprising amino acids 8 to 20.
The above identified amino acid regions of the respective immunoglobulins are loops or loop regions specified to be suitable for modification purposes according to the invention. Preferably combinations of such modifications, e.g. in at least two of the specified loops or loop regions, are engineered into the immunoglobulin according to the invention.
Preferably, a modification in the structural loop or loop region comprising amino acids 93 to 98 is combined with a modification in one or more of the other structural loops.
In a preferred embodiment a modification in the structural loop or loop region comprising amino acids 93 to 98 is combined with a modification in the structural loop region comprising amino acids 69 to 75.
Most preferably each of the structural loops comprising amino acids 93 to 98, amino acids 69 to 75 and amino acids 8 to 20 contain at least one amino acid modification.
In another preferred embodiment each of the structural loops comprising amino acids 93 to 98, amino acids 69 to 75, amino acids 44 to 50 and amino acids 8 to 20 contain at least one amino acid modification.
According to a preferred embodiment of the present invention the structural loops or loop regions of an immunoglobulin or the variable domain of the immunoglobulin of murine origin, e.g. a VH, comprise amino acids 6 to 20, amino acids 44 to 52, amino acids 67 to 76 and amino acids 92 to 101.
According to another preferred embodiment of the present invention the structural loops or loop regions of an immunoglobulins or the variable domain of the immunoglobulin of camelid origin, e.g. VHH, comprise amino acids 7 to 18, amino acids 43 to 55, amino acids 68 to 75 and amino acids 91 to 101.
The variable domains of camelid origin or humanized variants of camelid origin, have the advantage that they could easily be combined with other variable domains, for instance with other VHH of camelid origin, modified or native. The possible combination of VHH of camelid origin is the basis for multivalent immunoglobulins. Thus, according to the invention specific modified variable domains of camelid origin are multivalent combinations, preferably with at least 3, more preferably with at least 4 or 5 valencies or VHHs.
Preferably, the new antigen binding sites in the structural loops are introduced into the immunoglobulin encoded by the selected nucleic acid by substitution, deletion and/or insertion of at least one nucleotide.
According to another preferred embodiment of the present invention the modification of at least one nucleotide in each of at least two structural loops or loop regions result in a substitution, deletion and/or insertion in the immunoglobulin or immunoglobulin variable domain encoded by said nucleic acid.
The modification of the at least two loops or loop regions of an immunoglobulin or antibody variable domain may result in a substitution, deletion and/or insertion of 2 or more amino acids, preferably point mutations, change of amino acids of whole loops, more preferred the change of at least 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, up to 30 amino acids. However, the maximum number of amino acids inserted into a structural loops or loop regions of an immunoglobulin or immunoglobulin variable domain may in specific cases not exceed the number of 30, preferably 25, more preferably 20, amino acids.
Thereby the modified sequence comprises amino acids not included in the conserved regions of the structural loops, the newly introduced amino acids being naturally occurring, but foreign to the site of modification, or substitutes of naturally occurring amino acids. When the foreign amino acid is selected from a specific group of amino acids, such as amino acids with specific polarity, or hydrophobicity, a library enriched in the specific group of amino acids at the randomized positions can be obtained according to the invention. Such libraries are also called “focused” libraries.
The at least two loops or loop regions are preferably mutated or modified by random, semi-random or, in particular, by site-directed random mutagenesis methods.
A preferred method to introduce modifications is site directed random mutation. With this method two or more specific amino acid residues of the loops are exchanged or introduced using randomly generated inserts into such structural loops. Alternatively preferred is the use of combinatorial approaches.
In another preferred embodiment at least three structural loops or loop regions of an immunoglobulin or immunoglobulin variable domain are mutated or modified by random, semi-random or, in particular, by site-directed random mutagenesis methods.
These methods may be used to make amino acid modifications at desired positions of the immunoglobulins or immunoglobulin variable domain of the present invention. In these cases positions are chosen randomly, or amino acid changes are made using certain rules. For example certain residues may be mutated to any amino acids, whereas other residues may be mutated to a restricted set of amino acids. This can be achieved in a stepwise fashion by alternating of cycles of mutation and selection or simultaneously.
The randomly modified nucleic acid molecule may comprise the herein identified repeating units, which code for all known naturally occurring amino acids or a subset thereof. Those libraries that contain modified sequences wherein a specific subset of amino acids are used for modification purposes are called “focused” libraries. The member of such libraries have an increased probability of an amino acid of such a subset at the modified position, which is at least two times higher than usual, preferably at least 3 times or even at least 4 times higher. Such libraries have also a limited or lower number of library members, so that the number of actual library members reaches the number of theoretical library members. In some cases the number of library members of a focused library is not less than 103 times the theoretical number, preferably not less than 102 times, most preferably not less than 10 times.
A library according to the invention may be designed as a library containing or consisting of library members of a specific immunoglobulin format. Those libraries that are consisting of specific immunoglobulin molecular format are called dedicated library for the purpose of this invention. Dedicated libraries preferably contain a majority of the specific formats, at least 50%, preferably at least 60%, more preferred at least 70%, more preferred at least 80%, more preferred at least 90%, or those that essentially consist of specific antibody formats. Specific antibody formats are preferred, such that the preferred library according to the invention it is selected from the group consisting of a VH library, VHH library, Vkappa library, Vlambda library, Fab library, a CH1/CL library and a CH3 library. Libraries characterized by the content of composite molecules containing more than one antibody domains, such as an IgG library or Fc library are specially preferred. Other preferred libraries are those containing T-cell receptors, forming T-cell receptor libraries. Further preferred libraries are epitope libraries, wherein the fusion protein comprises a molecule with a variant of an epitope, also enabling the selection of competitive molecules having similar binding function, but different functionality. Exemplary is a TNFalpha library, wherein trimers of the TNFalpha fusion protein are displayed by a single genetic package.
However, the maximum number of amino acids inserted into a loop or loop region of an immunoglobulin preferably may not exceed the number of 30, preferably 25, more preferably 20 amino acids at a maximum. The substitution and the insertion of the amino acids occurs preferably randomly or semi-randomly using all possible amino acids or a selection of preferred amino acids for randomization purposes, by methods known in the art and as disclosed in the present patent application.
The site of modification may be at a specific single structural loop or a structural loop region. A loop region usually is composed of at least two, preferably at least 3 or at least 4 loops that are adjacent to each other, and which may contribute to the binding of an antigen through forming an antigen binding site or antigen binding pocket. It is preferred that the one or more sites of modification are located within the area of 10 amino acids, more preferably within 20, 30, 40, 50, 60, 70, 80, 90 up to 100 amino acids, in particular within a structural loop region to form a surface or pocket where the antigen can sterically access the loop regions.
The at least one loop or loop region is preferably mutated or modified to produce libraries, preferably by random, semi-random or, in particular, by site-directed random mutagenesis methods, in particular to delete, exchange or introduce randomly generated inserts into structural loops. Alternatively preferred is the use of combinatorial approaches. Any of the known mutagenesis methods may be employed, among them cassette mutagenesis. These methods may be used to make amino acid modifications at desired positions of the immunoglobulin of the present invention. In some cases positions are chosen randomly, e.g. with either any of the possible amino acids or a selection of preferred amino acids to randomize loop sequences, or amino acid changes are made using simplistic rules. For example all residues may be mutated preferably to specific amino acids, such as alanine, referred to as amino acid or alanine scanning. Such methods may be coupled with more sophisticated engineering approaches that employ selection methods to screen higher levels of sequence diversity.
A preferred method according to the invention refers to a randomly modified nucleic acid molecule coding for an immunoglobulin, immunoglobulin domain or a part thereof which comprises at least one nucleotide repeating unit within a structural loop coding region having the sequence 5′-NNS-3′, 5′-NNN-3′, 5′-NNB-3′ or 5′-NNK-3′. In some embodiments the modified nucleic acid comprises nucleotide codons selected from the group of TMT, WMT, BMT, RMC, RMG, MRT, SRC, KMT, RST, YMT, MKC, RSA, RRC, NNK, NNN, NNS or any combination thereof (the coding is according to IUPAC).
The randomly modified nucleic acid molecule may comprise the above identified repeating units, which code for all known naturally occurring amino acids or a subset thereof.
The modification of the nucleic acid molecule may be performed by introducing synthetic oligonucleotides into a larger segment of nucleic acid or by de novo synthesis of a complete nucleic acid molecule. Synthesis of nucleic acid may be performed with tri-nucleotide building blocks which would reduce the number of nonsense sequence combinations if a subset of amino acids is to be encoded (e.g. Yanez et al. Nucleic Acids Res. (2004) 32:e158; Virnekas et al. Nucleic Acids Res. (1994) 22:5600-5607).
Preferably the positions to be modified are surface exposed amino acids. Surface exposition of amino acids of structural loops can be judged from known protein structures of antibody variable domains and by analogy or homology for such amino acid sequences for which no experimentally determined structure is available.
In a preferred embodiment of the invention the modifications introduced into the at least two structural loops comprise at least 1, 2, 3, 4, 5 or 6 foreign amino acids or amino acids not naturally occurring at the respective site of the structural loop of the non-modified immunoglobulin or immunoglobulin variable domain.
The modification of amino acids may preferentially be biased in order to introduce into structural loops or loop regions amino acids which are known to be frequently involved in protein-protein interactions (e.g. Lea & Stewart (1995) FASEB J. 9:87-93; Fellhouse et al. (2006) J. Mol. Biol. 357:100-114; Adib-Conquuy et al. (1998) International Immunology 10:341-346; Lo Conte et al. (1999) J. Mol. Biol. 285:2177-2198; Zemlin et al. (2003) J. Mol. Biol. 334:733-749).
According to one embodiment of the invention an immunoglobulin obtainable by the method according to the invention is used for the preparation of a library with library members displaying or encoding the immunoglobulins according to the invention, specifically a library of proteins, fusion proteins, cells, in particular microbial cells, like bacterial or yeast cells, phages, viruses, nucleic acids or ribosomes.
The following specification not only refers to libraries of polypeptide or protein variants, but, of course, also to the alternative libraries used for expressing the immunoglobulins according to the invention, e.g. as mentioned above.
In one preferred embodiment, a library of polypeptide variants comprising immunoglobulins or immunoglobulin variable domains of the invention is used as a pool for selection wherein the modifications contain or introduce at least one, more preferably at least two amino acids per modified structural loop out of the group of amino acids tryptophane, tyrosine, phenylalanine, histidine, isoleucine, serine, methionine, alanine and asparagine.
It turned out that according to the invention a variant variable domain polypeptide can be provided with specific mutations that are foreign to the native polypeptides. Any of the amino acids tryptophane, tyrosine, phenylalanine, histidine, isoleucine, serine, methionine, alanine and asparagines are not present in the structural loops of human native immunoglobulins, thus are considered as “foreign”. A variant polypeptide according to the invention may contain at least two of said foreign amino acids in the structural loops, by modification of at least one structural loop and to make up a binding site.
If the modified immunoglobulin or immunoglobulin variable domain is of human origin or a humanized immunoglobulin variable domain, preferred modifications are the incorporation of least one tyrosine in any one of the positions 12 to 17, 45 to 50, 69 to 75 and 93 to 98, and/or at least one tryptophane in any one of the positions 12 to 17, 45 to 50, 69, 71 to 75, 93 to 94 and 96 to 98, and/or at least one histidine in any one of the positions 12 to 17, 46, 47, 49, 50, 69 to 74 and 93 to 98, and/or at least one asparagine in any one of the positions 12 to 17, 45 to 47, 49, 50, 70 to 73, 75, 94 to 96 and 98, and/or at least one methionine in any one of the positions 12 to 17, 46 to 50, 69 to 71, 73 to 75, 93, 95, 96 and 98, and/or at least one serine in any one of the positions 13, 71, 75, 94, 95 and 98, and/or at least one isoleucine in any one of the positions 12, 14 to 17, 45 to 50, 69, 70, 72 to 75, 93 and 96 to 98, and/or at least one phenylalanine in any one of the positions 15, 46, 48, 70 to 73, 75, 93, 95 and 98.
According to another preferred embodiment of the present invention at least two amino acid residues in positions 15 to 17, 29 to 34, 85.4 to 85.3, 92 to 94, 97 to 98 and/or 108 to 110 of a human or humanized single domain antibody are modified.
The nucleic acid molecules encoding the modified immunoglobulins or immunoglobulin variable domains (and always included throughout the whole specification: immunoglobulins and immunoglobulin fragments comprising a modified immunoglobulin variable domain) may be cloned into host cells, expressed and assayed for their binding specificities. These practices are carried out using well-known procedures, and a variety of methods that may find use in the present invention are described in Molecular Cloning—A Laboratory Manual, 3.sup.rd Ed. (Maniatis, Cold Spring Harbor Laboratory. Press, New York, 2001), and Current Protocols in Molecular Biology (John Wiley & Sons). The nucleic acids that encode the modified immunoglobulins or immunoglobulin variable domains of the present invention may be incorporated into an expression vector in order to express said immunoglobulins. Expression vectors typically comprise an immunoglobulin operably linked—that is placed in a functional relationship—with control or regulatory sequences, selectable markers, any fusion partners, and/or additional elements. The modified immunoglobulins of the present invention may be produced by culturing a host cell transformed with nucleic acid, preferably an expression vector, containing nucleic acid encoding the modified immunoglobulins, under the appropriate conditions to induce or cause expression of the modified immunoglobulins. The methods of introducing exogenous nucleic acid molecules into a host are well known in the art, and will vary with the host used. Of course, also non-cellular or cell-free expression systems for the expression of modified immunoglobulins may be employed.
In a preferred embodiment of the present invention, the modified immunoglobulins are purified or isolated after expression. Modified immunoglobulins may be isolated or purified in a variety of ways known to those skilled in the art. Standard purification methods include chromatographic techniques, electrophoretic, immunological, precipitation, dialysis, filtration, concentration, and chromatofocusing techniques. Purification can often be enabled by a particular fusion partner. For example, antibodies may be purified using glutathione resin if a GST fusion is employed, Ni2+-affinity chromatography if a His-tag is employed or immobilized anti-flag antibody if a flag-tag is used. For general guidance in suitable purification techniques, see e.g. Scopes, “Protein Purification: Principles and Practice”, 1994, 3rd ed., Springer-Science and Business Media Inc., NY or Roe, “Protein Purification Techniques: A Practical Approach”, 2001, Oxford University Press. Of course, it is also possible to express the modified immunoglobulins according to the present invention on the surface of a host, in particular on the surface of a bacterial, insect or yeast cell or on the surface of phages or viruses.
Modified immunoglobulins of the invention may be screened using a variety of methods, including but not limited to those that use in vitro assays, in vivo and cell-based assays, and selection technologies. Automation and high-throughput screening technologies may be utilized in the screening procedures. Screening may employ the use of a fusion partner or label, for example an enzyme, an immune label, isotopic label, or small molecule label such as a fluorescent or colorimetric dye or a luminogenic molecule.
In a preferred embodiment, the functional and/or biophysical properties of the immunoglobulins are screened in an in vitro assay. In a preferred embodiment, the antibody is screened for functionality, for example its ability to catalyze a reaction or its binding specificity, cross reactivity and/or affinity to its target.
In another preferred embodiment, the favourable modified immunoglobulin domains may be selected in vivo, e.g. by introducing it into a cell or an organism. The specifically binding variants may be isolated either from body fluid such as blood or lymphatic liquid or from specific organs, depending on the required properties of the modified domains.
Assays may employ a variety of detection methods including but not limited to chromogenic, fluorescent, luminescent, or isotopic labels.
As is well known in the art, there are a variety of selection technologies that may be used for the identification and isolation of proteins with certain binding characteristics and affinities, including, for example, display technologies such as phage display, ribosome display, cell surface display, and the like, as described below. Methods for production and screening of antibody variants are well known in the art. General methods for antibody molecular biology, expression, purification, and screening are described in Antibody Engineering, edited by Duebel & Kontermann, Springer-Verlag, Heidelberg, 2001; and Hayhurst & Georgiou, 2001, Curr Opin Chem Biol 5:683-689; Maynard & Georgiou, 2000, Annu Rev Biomed Eng 2:339-76.
As is known in the art, some screening methods select for favourable members of a library. The methods are herein referred to as “selection methods”, and these methods find use in the present invention for screening modified immunoglobulins. When variant immunoglobulin variable domain libraries are screened using a selection method, only those members of a library that are favourable, that is which meet some selection criteria, are propagated, isolated, and/or observed. As will be appreciated, because only the fittest variants are observed, such methods enable the screening of libraries that are larger than those screenable by methods that assay the fitness of library members individually. Selection is enabled by any method, technique, or fusion partner that links, covalently or non-covalently, the phenotype of immunoglobulins with its genotype that is the function of an antibody with the nucleic acid that encodes it. For example the use of phage display as a selection method is enabled by the fusion of library members to a phage coat protein (most frequently used is the filamentous bacteriophage gene III protein, however also other coat proteins such as protein VIII, protein VII, protein VI and protein IX can be used). In this way, selection or isolation of modified immunoglobulins that meet some criteria, for example binding affinity to the immunoglobulin's target, also selects for or isolates the nucleic acid that encodes it. Once isolated, the gene or genes encoding modified immunoglobulins may then be amplified. This process of isolation and amplification, referred to as panning, may be repeated, allowing favourable antibody variable domain variants in the library to be enriched. Nucleic acid sequencing of the attached nucleic acid ultimately allows for gene identification.
A variety of selection methods are known in the art that may find use in the present invention for screening immunoglobulin or immunoglobulin variable domain libraries. These include but are not limited to phage display (Phage display of peptides and antibodies: a laboratory manual, Kay et al., 1996, Academic Press, San Diego, Calif., 1996; Lowman et al., 1991, Biochemistry 30:10832-10838; Smith, 1985, Science 228:1315-1317) and its derivatives such as selective phage infection (Malmborg et al., 1997, J Mol Biol 273:544-551), selectively infective phage (Krebber et al., 1997, J Mol Biol 268:619-630), and delayed infectivity panning (Benhar et al., 2000, J Mol Biol 301:893-904), cell surface display (Witrrup, 2001, Curr Opin Biotechnol, 12:395-399) such as display on bacteria (Georgiou et al., 1997, Nat Biotechnol 15:29-34; Georgiou et al., 1993, Trends Biotechnol 11:6-10; Lee et al., 2000, Nat Biotechnol 18:645-648; Jun et al., 1998, Nat Biotechnol 16:576-80), yeast (Boder & Wittrup, 2000, Methods Enzymol 328:430-44; Boder & Wittrup, 1997, Nat Biotechnol 15:553-557), and mammalian cells (Whitehorn et al., 1995, Bio/technology 13:1215-1219), as well as in vitro display technologies (Amstutz et al., 2001, Curr Opin Biotechnol 12:400-405) such as polysome display (Mattheakis et al., 1994, Proc Natl Acad Sci USA 91:9022-9026), ribosome display (Hanes et al., 1997, Proc Natl Acad Sci USA 94:4937-4942), mRNA display (Roberts & Szostak, 1997, Proc Natl Acad Sci USA 94:12297-12302; Nemoto et al., 1997, FEBS Lett 414:405-408), and ribosome-inactivation display system (Zhou et al., 2002, J Am Chem Soc 124, 538-543).
Other selection methods that may find use in the present invention include methods that do not rely on display, such as in vivo methods including but not limited to periplasmic expression and cytometric screening (Chen et al., 2001, Nat Biotechnol 19:537-542), the antibody fragment complementation assay (Johnsson & Varshaysky, 1994, Proc Natl Acad Sci USA 91:10340-10344; Pelletier et al., 1998, Proc Natl Acad Sci USA 95:12141-12146), and the yeast two hybrid screen (Fields & Song, 1989, Nature 340:245-246) used in selection mode (Visintin et al., 1999, Proc Natl Acad Sci USA 96:11723-11728). In an alternate embodiment, selection is enabled by a fusion partner that binds to a specific sequence on the expression vector, thus linking covalently or noncovalently the fusion partner and associated immunoglobulin library member with the nucleic acid that encodes them. For example, WO9308278 describe such a fusion partner and technique that may find use in the present invention. In an alternative embodiment, in vivo selection can occur if expression of the antibody imparts some growth, reproduction, or survival advantage to the cell.
Some selection methods are referred to as “directed evolution” methods. Those methods include the mating or breeding of favourable sequences during selection, sometimes with the incorporation of new mutations. As will be appreciated by those skilled in the art, directed evolution methods can facilitate identification of the most favourable sequences in a plurality of polypeptides, and can increase the diversity of sequences that are screened. A variety of directed evolution methods are known in the art that may find use in the present invention for generating and screening antibody variable domain variants, including but not limited to DNA shuffling (PCT WO00/42561; PCT WO 01/70947), exon shuffling (Kolkman & Stemmer, 2001, Nat Biotechnol 19:423-428), family shuffling (Crameri et al., 1998, Nature 391:288-291), selective combinatorial randomization (WO03012100, WO04018674A1), Random Chimeragenesis on Transient Templates (Coco et al., 2001, Nat Biotechnol 19:354-359), molecular evolution by staggered extension process (StEP) in vitro recombination (Zhao et al., 1998, Nat Biotechnol 16:258-261; Shao et al., 1998, Nucleic Acids Res 26:681-683), exonuclease mediated gene assembly (U.S. Pat. No. 6,352,842; U.S. Pat. No. 6,361,974), Gene Site Saturation Mutagenesis (U.S. Pat. No. 6,358,709), Gene Reassembly (U.S. Pat. No. 6,358,709), SCRATCHY (Lutz et al., 2001, Proc Natl Aced Sci USA 98:11248-11253), DNA fragmentation methods (Kikuchi et al., Gene 236:159-167), single-stranded DNA shuffling (Kikuchi et al., 2000, Gene 243:133-137), and directed evolution antibody engineering technology (Applied Molecular Evolution) (U.S. Pat. No. 5,824,514; U.S. Pat. No. 5,817,483; U.S. Pat. No. 5,814,476; U.S. Pat. No. 5,763,192; U.S. Pat. No. 5,723,323).
In a preferred embodiment, immunoglobulins or antibody variable domain variants are screened using one or more cell-based or in vivo assays. For such assays, purified or non-purified modified immunoglobulins or immunoglobulin variable domains are typically added exogenously such that cells are exposed to individual immunoglobulins or modified immunoglobulin variable domains or pools of modified immunoglobulin variable domains belonging to a library. These assays are typically, but not always, based on the desired function of the immunoglobulin or immunoglobulin variable domain; that is, the ability of the antibody or antibody variable domain modified according to the invention to bind to its target and to mediate some biochemical event, for example effector function, ligand/receptor binding inhibition, apoptosis, and the like. Such assays often involve monitoring the response of cells to the antibody variable domain, for example cell survival, cell death, change in cellular morphology, or transcriptional activation such as cellular expression of a natural gene or reporter gene. For example, such assays may measure the ability of variable immunoglobulin domain variants to elicit ADCC, ADCP or CDC. For some assays additional cells or components, that is in addition to the target cells, may need to be added, for example serum complement, or effector cells such as peripheral blood monocytes (PBMCs), NK cells, macrophages, and the like. Such additional cells may be from any organism, preferably humans, mice, rat, rabbit, and monkey. Immunoglobulins may cause apoptosis of certain cell lines expressing the target, or they may mediate attack on target cells by immune cells which have been added to the assay. Methods for monitoring cell death or viability are known in the art, and include the use of dyes, immunochemical, cytochemical, and radioactive reagents. For example, caspase staining assays may enable to measure apoptosis, and uptake or release of radioactive substrates or fluorescent dyes may enable cell growth or activation to be monitored.
Alternatively, dead or damaged target cells may be monitored by measuring the release of one or more natural intracellular components, e.g. lactate dehydrogenase. Transcriptional activation may also serve as a method for assaying function in cell-based assays. In this case, response may be monitored by assaying for natural genes which may be upregulated, for example the release of certain interleukins may be measured, or alternatively readout may be via a reporter system. Cell-based assays may also involve the measure of morphological changes of cells as a response to the presence of modified immunoglobulin variable domains. Cell types for such assays may be prokaryotic or eukaryotic, and a variety of cell lines that are known in the art may be employed.
Alternatively, cell-based screens may be performed using cells that have been transformed or transfected with nucleic acids encoding the variant immunoglobulin variable domains. In this case, antibody variable domain variants of the invention are not added exogenously to the cells (e.g. Auf der Maur, 2004, Methods, 34:215-224). In another alternative method, the cell-based screen utilizes cell surface display. A fusion partner can be employed that enables display of modified immunoglobulin variable domains on the surface of cells (Witrrup, 2001, Curr Opin Biotechnol, 12:395-399).
In a preferred embodiment, the immunogenicity of the modified immunoglobulins may be changed and determined experimentally using one or more immunological or cell based assays (e.g. Koren et al., 2002, Current Pharmaceutical Biotechnology 3:349-360; Chirino et al., 2004, Drug Discovery Today 9:82-90; Tangri et al., 2005, J. Immunol. 174:3187-3196; Hermeling et al., 2004, Pharm. Res. 21:897-903). In a preferred embodiment, ex vivo T-cell activation assays are used to experimentally quantitate immunogenicity. In this method, antigen-presenting cells and naive T-cells from matched donors are challenged with a peptide or whole antibody or immunoglobulin of interest one or more times. T-cell activation can be detected using a number of methods, e.g. by monitoring of cytokine release or measuring uptake of tritiated thymidine. In preferred embodiments, LUMINEX technology is used to measure cytokine release (e.g. de Jager et al., Clin. Diagn. Lab. Immunol., 2003, 10:133-139) or interferon gamma production is monitored using Elispot assays (Schmittel et. al., 2000, J. Immunol. Meth., 24: 17-24).
The biological or functional properties of the modified immunoglobulins or immunoglobulin variable domains of the present invention may be characterized in cell, tissue, and whole organism experiments. As is known in the art, drugs are often tested in animals, including but not limited to mice, rats, rabbits, dogs, cats, pigs, and monkeys, in order to measure a drug's efficacy for treatment against a disease or disease model, or to measure a drug's pharmacokinetics, toxicity, and other properties. The animals may be referred to as disease models. Therapeutics are often tested in mice, including but not limited to nude mice, SCID mice, xenograft mice, and transgenic mice (including genetic knock-in and knock-out mutants). Such experimentation may provide meaningful data for determination of the potential of the polypeptide variant to be used as a therapeutic. Any organism, preferably mammals, may be used for testing. Because of their genetic similarity to humans, monkeys can be suitable therapeutic models, and thus may be used to test the efficacy, toxicity, pharmacokinetics, or other property of the modified immunoglobulins of the present invention. Testing drug candidates in humans are mostly required for approval as therapeutics, and thus of course these experiments are contemplated. Thus the modified immunoglobulins or immunoglobulin variable domains of the present invention may be tested in humans to determine their therapeutic efficacy, toxicity, immunogenicity, pharmacokinetics, pharmacodynamics and/or other clinical properties.
The immunoglobulin according to the present invention may be used for any purpose known in the art for immunoglobulins but also enables applications which are depending on the combination of specificities introduced by the present invention.
In one embodiment the antibody variant of the present invention is used for therapy or prophylaxis, for preparative or analytic use, as a diagnostic, an industrial compound or a research reagent, preferably a therapeutic. The antibody variant may find use in an antibody composition that is monoclonal, oligoclonal or polyclonal. In a preferred embodiment, the modified immunoglobulins or immunoglobulin variable domains of the present invention are used to kill target cells that bear the target antigen, for example cancer cells. In an alternate embodiment, the modified immunoglobulins of the present invention are used to block, antagonize, or agonize the target antigen, for example by antagonizing a cytokine or cytokine receptor. In an alternately preferred embodiment, the modified immunoglobulins of the present invention are used to block, antagonize, or agonize the target antigen and kill the target cells that bear the target antigen.
In an alternately preferred embodiment, the modified immunoglobulins of the present invention are used to block, antagonize, or agonize growth factors or growth factor receptors and kill the target cells that bear or need the target antigen. In an alternately preferred embodiment, the modified immunoglobulins of the present invention are used to block, antagonize, or agonize enzymes and substrate of enzymes.
In another alternatively preferred embodiment, the modified immunoglobulin variable domains of the present invention are used to neutralize infectious agents such as viruses, small viruses, prions, bacteria or fungi.
The modified immunoglobulins or immunoglobulins variable domains of the present invention may be used for various therapeutic purposes. In a preferred embodiment, an antibody comprising the modified immunoglobulin or immunoglobulin variable domain is administered to a patient to treat a specific disorder. A “patient” for the purposes of the present invention includes both, humans and other animals, preferably mammals and most preferably humans. By “specific disorder” herein is meant a disorder that may be ameliorated by the administration of a pharmaceutical composition comprising a modified immunoglobulin or immunoglobulin variable domain of the present invention.
In one embodiment, a modified immunoglobulin or immunoglobulin variable domain according to the present invention is the only therapeutically active agent administered to a patient. Alternatively, the modified immunoglobulin or immunoglobulin variable domain according the present invention is administered in combination with one or more other therapeutic agents, including but not limited to cytotoxic agents, chemotherapeutic agents, cytokines, growth inhibitory agents, anti-hormonal agents, kinase inhibitors, anti-angiogenic agents, cardioprotectants, or other therapeutic agents. The modified immunoglobulin or immunoglobulin variable domain may be administered concomitantly with one or more other therapeutic regimens. For example, an antibody variant of the present invention may be formulated and administered to the patient along with chemotherapy, radiation therapy, or both chemotherapy and radiation therapy. In one embodiment, the modified immunoglobulin or immunoglobulin variable domain of the present invention may be administered in conjunction with one or more antibodies, which may or may not comprise an antibody variant of the present invention. In accordance with another embodiment of the invention, the modified immunoglobulin or immunoglobulin variable domain of the present invention and one or more other anti-cancer therapies are employed to treat cancer cells ex vivo. It is contemplated that such ex vivo treatment may be useful in bone marrow transplantation and particularly, autologous bone marrow transplantation. It is of course contemplated that the antibodies of the invention can be employed in combination with still other therapeutic techniques such as surgery.
A variety of other therapeutic agents may find use for administration with the modified immunoglobulins of the present invention. In one embodiment, the modified immunoglobulin is administered with an anti-angiogenic agent, which is a compound that blocks, or interferes to some degree with the development of blood vessels. The anti-angiogenic factor may, for instance, be a small molecule or a protein, for example an antibody, Fc fusion, or cytokine, that binds to a growth factor or growth factor receptor involved in promoting angiogenesis. The preferred anti-angiogenic factor herein is an antibody that binds to Vascular Endothelial Growth Factor (VEGF). In an alternate embodiment, the modified immunoglobulin is administered with a therapeutic agent that induces or enhances adaptive immune response, for example an antibody that targets CTLA-4. In an alternate embodiment, the modified immunoglobulin is administered with a tyrosine kinase inhibitor, which is a molecule that inhibits to some extent tyrosine kinase activity of a tyrosine kinase. In an alternate embodiment, the modified immunoglobulins of the present invention are administered with a cytokine. By “cytokine” as used herein is meant a generic term for proteins released by one cell population that act on another cell as intercellular mediators including chemokines.
Pharmaceutical compositions are contemplated wherein modified immunoglobulins of the present invention and one or more therapeutically active agents are formulated. Formulations of the polypeptide variants of the present invention are prepared for storage by mixing said modified immunoglobulin or immunoglobulin variable domain having the desired degree of purity with optional pharmaceutically acceptable carriers, excipients or stabilizers (Remington's Pharmaceutical Sciences, 1980, 16th edition, Osol, A. Ed.,), in the form of lyophilized formulations or aqueous solutions. The formulations to be used for in vivo administration are preferably sterile. This is readily accomplished by filtration through sterile filtration membranes or other methods. The modified immunoglobulins and other therapeutically active agents disclosed herein may also be formulated as immunoliposomes, and/or entrapped in microcapsules.
Administration of the pharmaceutical composition comprising a modified immunoglobulin or immunoglobulin variable domain of the present invention, preferably in the form of a sterile aqueous solution, may be performed in a variety of ways, including, but not limited to, orally, subcutaneously, intravenously, intranasally, intraotically, transdermally, topically (e.g., gels, salves, lotions, creams, etc.), intraperitoneally, intramuscularly, intrapulmonary, vaginally, parenterally, rectally, or intraocularly.
Another aspect of the present invention relates to a method for manufacturing a molecule comprised of an immunoglobulin or immunoglobulin variable domain or a pharmaceutical preparation thereof comprising at least one modification in each of two structural loops or loop regions of said immunoglobulin or immunoglobulin variable domain and determining the binding of said molecule to an epitope of an antigen, wherein the unmodified molecule does not significantly bind to said epitope, comprising the steps of:
In particular the present invention relates to a method for manufacturing a multi-specific molecule binding specifically to at least one first molecule or a pharmaceutical preparation thereof comprising at least one modification in each of at least two structural loops or loop regions of an immunoglobulin or immunoglobulin variable domain and determining the specific binding of said at least two loops or loop regions to at least one second molecule selected from antigens. The immunoglobulin or immunoglobulin variable domain containing an unmodified structural loops or loop regions does not specifically bind to said at least one second molecule.
The method specifically comprises the steps of:
The engineering of more than one binding site or at least two specificities into a member of a specific binding pair is preferred (Kufer et al. (2004) Trends in Biotechnology vol. 22 pages 238-244).
Numerous attempts have been made to produce multi-specific, e.g. bispecific, monoclonal antibodies or antibody fragments. One problem in the production of bispecific antibodies made of two different polypeptide chains (heavy and light chain) is the necessity to express four different chains (two heavy and two light chains) in one cell resulting in a number of various combinations of molecules which have to be separated from the desired bispecific molecule in the mixture. Due to their similarity the separation of these molecules is difficult and expensive. A number of techniques have been employed to minimize the occurrence of such unwanted pairings (Carter (2001) Journal of Immunological Methods, vol 248, pages 7-15)
One solution to the problem is the production of one polypeptide chain with two specificities, like e.g. two scFvs linked to each other or the production of so-called diabodies. Such molecules have been shown to be far away from the fold of a natural molecule and are notoriously difficult to produce (LeGall et al. (2004) Protein Engineering, Design & Selection vol 17 pages 357-366).
According to a preferred embodiment of the present invention the expression system comprises a vector. Any expression vector known in the art may be used for this purpose as appropriate.
The modified immunoglobulin is preferably expressed in a host, preferably in a bacterium, in yeast, in a plant cell, in an insect cell, in an animal cell or mammalian cell or in an organ of a plant or animal or in a complete plant or animal.
A wide variety of appropriate host cells may be used to express the modified polypeptide of the invention, including but not limited to mammalian cells (animal cells) plant cells, bacteria (e.g. Bacillus subtilis, Escherichia coli), insect cells, and yeast (e.g. Pichia pastoris, Saccharomyces cerevisiae). For example, a variety of cell lines that may find use in the present invention are described in the ATCC cell line catalog, available from the American Type Culture Collection. Furthermore, also plants and animals may be used as hosts for the expression of the immunoglobulin according to the present invention. The expression as well as the transfection vectors or cassettes may be selected according to the host used.
Of course also non-cellular or cell-free protein expression systems may be used. In vitro transcription/translation protein expression platforms, that produce sufficient amounts of protein offer many advantages of a cell-free protein expression, eliminating the need for laborious up- and down-stream steps (e.g. host cell transformation, culturing, or lysis) typically associated with cell-based expression systems.
Another problem of the current design of bispecific antibodies is the fact that even if the parent antibodies are bivalently binding to their respective binding partner (e.g. IgG), the resulting bispecific antibody is monovalent for each of the respective binding partner.
The preferred multi-specific molecules of the present invention solve these problems:
Expression of a bispecific molecule as one polypeptide chain is possible (a modified immunoglobulin variable domain with two binding specificities, see example section), which is easier to accomplish than the expression of two antibody polypeptide chains (Cabilly et al. Proc. Natl. Acad. Sci. USA 81:3273-3277 (1984).
It can also be produced as an antibody like molecule (i.e. made of 2 polypeptide chains). Due to the fact that the second specificity is located in the non-CDR part of the variable domains there is no need for two different heavy chains or different light chains. Thus, there is no possibility of wrong pairing of the two chains.
An antibody of the present invention may consist of a heavy chain and a light chain, which form together a variable CDR loop region binding to a specific binding partner, i.e. a specific CDR loop conformation, and the second specificity may be formed by modified structural loops or loop regions contained in the immunoglobulin molecule, e.g. the structural loops of either the heavy chain or the light chain variable domain, while maintaining the specific CDR loop conformation. The binding site may also be formed by at least one or more than one non-CDR loops on two, variable domains (e.g. a heavy chain variable domain and a light chain variable domain which may be structurally neighboured).
The modified antibody may be a complete antibody or an antibody fragment (e.g. Fab, scFv, Fv, minibody, dAb) comprising at least one immunoglobulin variable domain and modifications in the structural loops or loop regions, or derivatives thereof.
It may bind mono- or multivalently to binding partners or even with different valency for the different binding partners, depending on the design. For example, an Fab fragment or, equivalently an scFv may be engineered in such a way that the structural loops of the VH and the VL domains are separately engineered to bind to the same epitope as the binding site formed by the CDRs, resulting in a trivalent Fab fragment or scFv respectively. In another embodiment, a complete immunoglobulin containing the same engineered VH and VL domains will bind hexavalently to its target epitope. If for example the natural binding site formed by the CDRs recognizes a different target epitope than the engineered Vh and Vl domains then the resulting Fab fragment or scFv will bind monovalently to the first target, and bivalently to the second target which is bound independently by the modified structural loops of the VH and the VL domain respectively. This modular design principle can be applied in numerous different ways as will be obvious to those skilled in the art.
As there are a number of various structural loops available for selection and design of a specific binding site in the non-CDR regions of heavy and light domains it is possible to design antibody derivatives with even more than two specificities. For example, VH and VL domains recognizing a first target by their CDRs can be engineered separately to bind specifically to different (second and third) targets through interactions mediated by the modified structural loops. Thus, a trispecific Fab fragment or scFv, which binds monovalenty to each of its target can be generated. If the modified variable domains of this Fab are engineered in the form of a full size IgG, an engineered IgG is generated which is trispecific and, to each if its three specificities, binds bivalently.
The specific binding domains within one polypeptide chain may be connected with or without a peptide linker.
Some antibody classes can be regarded as multi-specific, in particular bispecific, by nature: They bind to an antigen (which is typically e.g. either a foreign structure or a cancer associated structure) with the variable region and they bind to Fc-effector molecules with the Fc part (e.g. Fc receptors on various immune cells or complement protein) thus enabling effects such as ADCC, ADCP or CDC.
The Fc-effector molecules are bound by the Fc-part of an immunoglobulin molecule (for IgG1 it consists of domains CH2 and CH3) and a number of methods have been described to optimize effector function by improvement of binding of the Fc-part of an antibody molecule either by glycoengineering techniques (U.S. Pat. No. 6,602,684) or by protein engineering either directly at the Fc (US 2005/0054832) or indirectly by engineering outside the Fc (US 2005/02444403). Both, binding of the Fc region to Fc receptor and/or binding to complement proteins such Cq1 has been altered by such techniques. Usually one tries to improve the binding affinity to such Fc-effector molecules as this correlates with improved effector functions.
With the current invention it is possible to design an antibody binding to Fc-effector molecules outside the natural Fc binding region. Modified loops in antibody variable domains other than the loops involved in “natural” Fc-effector molecule binding can be selected from a library of modified loop structures or designed to bind to one or more Fc-effector molecules. An antibody with such additional Fc-effector molecule binding sites would either have stronger avidity to a certain Fc-effector molecule or effector-cell displaying an Fc-effector molecule and therefore may have an even stronger effect than glycoengineered antibodies or otherwise improved Fc regions.
Antibody fragments have certain advantages as compared to whole antibodies. Fragments have usually good biodistribution properties and can more easily be produced. However, most of the antibody fragment designs lack effector functions and have short in vivo half life (Holliger P, et al. Nat Biotechnol. (2005) 23:1126-36.). Neither CH1 nor Cκ or Cλ domains are able to mediate effector functions, which is the reason why Fab molecules usually do not show ADCC, ADCP or CDC.
WO 02/44215 describes binding molecules which consist of the antigen binding site of an antibody and a peptide binding Fc-effector molecules. In such a way an antibody fragment displaying effector functions can be constructed. The peptide is being incorporated into the binding molecule at a position that does neither destroy the antigen binding nor the ability of the peptide to bind to an Fc-effector molecule.
According to the present invention however, the binding to Fc-effector molecules may be performed with modified immunoglobulins or immunoglobulin variable domains which have been selected for Fc-effector molecule binding from libraries of two, three or four randomized structural loop sequences within a fixed scaffold of an immunoglobulin or immunoglobulin variable domain. Therefore, it is possible to select for specific loop sequences which would not bind to Fc-effector molecules if isolated from the Ig-domain scaffold. The polypeptides resulting from the present invention may therefore preferably consist of more than 100 amino acids and may comprise one or more immunoglobulin variable domains.
In order to select for potential effector function of such variable domains according to the present invention, antibody- or antibody fragment libraries comprising mutant variable domains may be selected for binding to Fc-receptors and/or complement factors such as C1q. Fcgamma receptors for selection may be provided either on the surface of cells expressing naturally the respective receptors or by expression and purification of the extracellular part of the respective receptor. IFN-g stimulated U937 cells (CRL-1503, American Type Culture Collection) can be used as target cells for the isolation of phage displayed modified immunoglobulin variable domains that bind specifically to the high-affinity IgG receptor, FcgammaRI (Berntzen et al., 2006, Protein Eng Des Sel. 19(3):121-8). Binding to the Fc receptor can be tested for by FACS using U937 cells as target, which cells are stained specifically with selected modified immunoglobulin variable domains. Furthermore, the extracellular domains of human Fcgamma receptors can be cloned and expressed as soluble proteins or fusion proteins and used for analysis of the specific binding of potential binding partners (e.g. as in Berntzen et al., 2005, J Immunol Methods. 298(1-2):93-104). The identification and characterisation of modified immunoglobulin variable domains specifically binding to complement factor C1q can be performed essentially similarily (e.g. as in Lauvrak et al. 1997 Biol Chem. 378(12):1509-19).
In order to increase in vivo half life of a molecule consisting of or containing such a variable domain binding to FcRn, or serum albumin may be selected for with libraries of mutant variable domains according to the present invention. Those modified structural loops responsible for extending the half life of a molecule through its specific binding to scrum proteins or complement proteins can be used as isolated structural loops or in the context of an immunoglobulin or parts thereof, for combination with those molecules that are to be designed as molecules with increased half life in vivo.
FcRn receptors or other cell receptors for selection may be provided either on the surface of cells expressing naturally the respective receptors or by expression and purification of the extracellular part of the respective receptor. For the purpose of this invention a first screening on FcRn may select for mutant variable domains (or molecules comprising such mutant variable domains) which can further be tested in vitro and even further characterized in FACS experiments by binding to cells expressing FcRn receptor. Screening and selection may also consider pH dependencies in binding to FcRn (as described in PCT WO02/060919; PCT WO97/34631). It can be further characterized by affinity ranking of binding to various recombinant FcRn, isoforms and allotypes e.g with surface plasmon resonance techniques (e.g. as in Dall' Acqua et al. Journal of Immunology, 2002, 169: 5171-5180).
The modified immunoglobulin according to the invention may comprise a heavy and/or light chain, or parts thereof, and at least one variable domain.
The immunoglobulin according to the present invention comprises preferably at least one constant and/or at least one variable domain of the immunoglobulin, or a part thereof.
A variable domain usually is considered an immunoglobulin fold unit of the variable part of an immunoglobulin, also referred to as a domain of the variable region (e.g. VH, Vk, Vl, Vd)
Another preferred immunoglobulin according to the invention consists of a variable domain of a heavy or light chain, or a part thereof, with at least two structural loops or loop regions, and is characterised in that said at least two structural loops or loop regions comprise at least two amino acid modifications forming at least two modified structural loops or loop regions, wherein said at least two modified structural loops or loop regions bind specifically to at least one epitope of an antigen. In such a preferred immunoglobulin according to the invention the at least two amino acid modifications may be located in one or two structural loops or loop regions or at one or two structural loops so to make up a binding site for an antigen.
According to a preferred embodiment of the present invention the specific binding of the modified polypeptide to a molecule is determined by a binding assay selected from the group consisting of immunological assays, preferably enzyme linked immunosorbent assays (ELISA), surface plasmon resonance assays, saturation transfer difference nuclear magnetic resonance spectroscopy, transfer NOE (trNOE) nuclear magnetic resonance spectroscopy, competitive assays, tissue binding assays, live cell binding assays and cellular extract assays.
Binding assays can be carried out using a variety of methods known in the art, including but not limited to FRET (Fluorescence Resonance Energy Transfer) and BRET (Bioluminescence Resonance Energy Transfer)-based assays, Amplified Luminescent Proximity Homogeneous Assay, Scintillation Proximity Assay, ELISA (Enzyme-Linked Immunosorbent Assay), SPR (Surface Plasmon Resonance), isothermal titration calorimetry, differential scanning calorimetry, gel electrophoresis, and chromatography including gel filtration.
The modified polypeptide of the invention is preferably conjugated to a label selected from the group consisting of organic molecules, enzyme labels, radioactive labels, colored labels, fluorescent labels, chromogenic labels, luminescent labels, haptens, digoxigenin, biotin, metal complexes, metals, colloidal gold and mixtures thereof.
Modified polypeptides conjugated to labels as specified above may be used, for instance, in diagnostic methods.
The modified immunoglobulin may be conjugated to other molecules which allow the simple detection of said conjugate in, for instance, binding assays (e.g. ELISA) and binding studies.
Another aspect of the present invention relates to a polypeptide comprising a variable domain of a light or heavy chain or combinations thereof, with at least two loops or loop regions, characterised in that said at least two structural loops or loop regions each comprise at least one amino acid modification forming at least two modified structural loops or loop regions, wherein said at least two modified structural loops or loop regions bind specifically to at least one epitope of an antigen.
It is preferred to combine molecularly at least one modified antibody variable domain (=binding to the specific partner via the non-variable sequences or structural loops) with at least one other binding molecule which can be an antibody, antibody fragment, a soluble receptor, a ligand or another modified antibody domain.
The other binding molecule combined with the at least one modified antibody variable domain of the invention is selected from the group consisting of proteinaceous molecules, nucleic acids, and carbohydrates.
The structural loops or loop regions of the modified immunoglobulin according to the invention may specifically bind to any kind of binding molecules, in particular to proteinaceous molecules, proteins, peptides, polypeptides, nucleic acids, glycans, carbohydrates, lipids, small and large organic molecules, inorganic molecules. Of course, the modified immunoglobulin according to the invention may comprise at least two loops or loop regions whereby each of the loops or loop regions may specifically bind to different molecules or epitopes.
Another aspect of the present invention relates to the use of an immunoglobulin or immunoglobulin variable domain according to the present invention or obtainable by a method according to the present invention for the preparation of a vaccine for active immunization. Hereby the immunoglobulin is either used as antigenic drug substance to formulate a vaccine or used for fishing or capturing antigenic structures for use in a vaccine formulation.
Another aspect of the present invention relates to the use of an immunoglobulin according to the present invention or obtainable by a method according to the present invention for the preparation of a library of polypeptides comprising modified immunoglobulin variable domains.
Yet another aspect of the present invention relates to a method for specifically binding and/or detecting a target molecule comprising the steps of:
A preferred method according to the invention is for specifically binding and/or detecting a molecule comprising the steps of:
Test samples may be human or animal sample, such as blood samples or other body fluids and cell suspensions, which sample possibly contains a target molecule to be specifically bound by immunoglobulins for capturing and/or detecting purposes.
Another aspect of the present invention relates to a method for specifically isolating a target molecule comprising the steps of:
A preferred method according to the invention is for specifically isolating a modified immunoglobulin binding to a molecule comprising the steps of:
Those samples are usually considered sources for preparative isolating those molecules, for instance complex natural sources, like animal, human or plant sources or microbial derived sources or cell suspensions and cultures.
The immunoglobulins or immunoglobulin variable domains according to the present invention may be used to isolate specifically target molecules from a sample. If multi-specific immunoglobulins or immunoglobulin variable domains are used more than one target molecule may be isolated from a sample. It is especially advantageous using immunoglobulins or modified immunoglobulin variable domains in such methods because it allows, e.g., to generate a matrix having a homogeneous surface with defined amounts of binding partners (i.e. modified immunoglobulin variable domains) immobilised thereon which are able to bind to the target molecules to be isolated. In contrast thereto, if mono-specific binding partners are used no homogeneous matrix can be generated because the single binding partners do not bind with the same efficiency to the matrix.
Another aspect of the present invention relates to a method for targeting a compound to a target comprising the steps of:
Modified immunoglobulins or immunoglobulin variable domains according to the present invention may be used to deliver at least one compound bound to the CDRs by a specific CDR loop conformation to a target by binding to the modified structural loop region. Such immunoglobulins may be used to target therapeutic substances to a preferred site of action in the course of the treatment of a disease.
Another aspect of the present invention relates to a molecule library comprising, expressing or encoding an immunoglobulin or immunoglobulin variable domain according to the present invention or obtainable by the method according to the present invention.
The preferred library of immunoglobulins or immunoglobulin variable domains according to the invention comprises at least 10 immunoglobulins or immunoglobulin variable domains, preferably 100, more preferably 1000, more preferably 10000, more preferably 100000, most preferably more than 1000000 variant immunoglobulins or variable domains, with a modification in at least two structural loops or loop regions.
Usually libraries according to the invention comprise at least 10 fusion proteins or binding agents, preferably at least 100, more preferred at least 1000, more preferred at least 104, more preferred at least 105, more preferred at least 106, more preferred at least 107, more preferred at least 108, more preferred at least 109, more preferred at least 1010, more preferred at least 1011, up to 1012, in cases of ribosomal display even higher number are feasible.
It turned out that most preferred members of a library have mutations of at least 4, or even at least 5 or 6 amino acid positions in at least two structural loops or loop regions. Thus, the particularly preferred libraries according to the invention consist of members that have mutations of at least 2, 3 or 4 amino acid positions in at least two structural loops.
A library according to the invention may also comprises or consist of one of or a mixture of immunoglobulin variable domains selected from the group of VH, Vkappa, Vlambda and VHH, as suitable for the purpose of defining binding partners for commercial reasons.
Preferred methods for constructing said library can be found above and in the examples. The library according to the present invention may be used to identify immunoglobulins or immunoglobulin variable domains binding to a distinct molecule.
In particular the present invention relates to the use of a protein library of polypeptides comprising an immunoglobulins or immunoglobulin variable domain according to the present invention or obtainable by the method according to the present invention for the design of immunoglobulin derivatives.
An existing immunoglobulin can be changed to introduce antigen binding sites into an immunoglobulin or a variable domain by using a protein library of the respective immunoglobulin or variable domain of at least 10, preferably 100, more preferably 1000, more preferably 10000, more preferably 100000, most preferably more than 1000000 immunoglobulins or variant variable domains each with at least two modified structural loops. The library is then screened for binding to the specific antigen. After molecular characterization for the desired properties the selected immunoglobulin or variable domain is cloned into the original immunoglobulin by genetic engineering techniques so that it replaces the wild type region. Alternatively, only the DNA coding for the modified loops or coding for the mutated amino acids may be exchanged to obtain an immunoglobulin with the additional binding site for the specific antigen. Alternatively, the modification in the structural loops of the variable domains may be performed with the variable domain in its natural context, e.g. in the form of a Fab, scFv, or complete immunoglobulin molecule. Except when single domain immunoglobulins, a chain of single immunoglobulin domains or single chain immunoglobulins, such as scFv or unibodies (monovalent immunoglobulin fragments) are produced, usually the immunoglobulin according to the invention is provided as a dimer, preferably as a heterodimer.
The choice of the site for the mutated, antigen-specific structural loop is dependent on the structure of the original immunoglobulin and on the purpose of the additional binding site. If, for example, the original or parent immunoglobulin is a Fab or scFv, modification of at least two structural loops in the variable domains of the light chain and/or the heavy chain is possible, but also modification of at least two structural loops in the CH1/CL is preferred to produce an immunoglobulin according to the invention. Thus, the Fab molecule according to the invention may contain the new binding site through a modified loop region in the CH1 and or the CL domain. In this context it is usually of primary importance to maintain the specific CDR loop conformation and natural binding properties of the parent immunoglobulin, scFv or Fab.
To generate a library one may prepare libraries of mutant original molecules which have mutations in two ore more structural loops of one or more variable domains. The selection with complete mutated original molecules may have some advantages as the selection for antigen binding with a modified structural loop will deliver the sterically advantageous modifications. For example, if the complete molecule is a scFv, it may be advantageous to screen the library of mutated original scFv for binding to an antigen, followed by screening the specific binders for binding to the antigen which is recognized by the CDR loops (original specificity). In an alternative selection procedure the original—the first—antigen may be bound to the CDR-loops during the screening for binding to an antigen with the modified structural loops. This simultaneous screening may allow for rescuing of clones that would be lost during a sequential selection procedure if the binding to the antigen is influenced by the binding to the first antigen.
A preferred embodiment of the invention is a library of variant immunoglobulins containing or consisting of variable domains with at least one variant amino acid position in each of at least two of the structural loops. The library may comprise immunoglobulin domains of the heavy and the light chain or mixtures and molecular combinations thereof.
Another preferred embodiment is a library containing or consisting of VHH domains or humanized forms of such camelid domains with at least one variant amino acid position in each of at least two structural loops or loop regions.
Another preferred embodiment of the invention is a library containing or consisting of single chain antibodies, such as a scFv library with at least one variant amino acid position in each of at least two of the structural loops or loop regions of any of the variable domains of the single chain antibody or scFv.
Another preferred embodiment of the invention is a diabody library containing or consisting of at least one variant amino acid position in each of at least two of the structural loops or loop regions of any of the variable domains of the diabody.
Another preferred embodiment of the invention is a minibody library containing or consisting of at least one variant amino acid position in each of at least two of the structural loops or loop regions of any of the variable domains of the minibody.
Yet another preferred embodiment of the invention is a Fab library containing or Consisting of at least one variant amino acid position in each of at least two of the structural loops or loop regions of any of the variable domains of the Fab.
Yet another preferred embodiment of the invention is an antibody or IgG library, preferably a human antibody library, containing or consisting of at least one variant amino acid position in each of at least two of the structural loops or loop regions of any of the variable domains of the antibody or IgG domains.
The size requirement (i.e. the number of variants) of a library according to the invention, comprising differently mutated immunoglobulins or immunoglobulin variable domains or fusion molecules of mutated variable antibody domains is dependent on the task. In general, a library to generate an antigen binding site de novo needs to be larger than a library used to further modify an already existing engineered antigen binding site formed by a modified structural loop or loop region (e.g. for enhancing affinity or changing fine specificity to the antigen).
The present invention also relates to a polypeptide library or a nucleic acid library comprising a plurality of polypeptides comprising immunoglobulins or immunoglobulin variable domains or at least two structural loops or loop regions contained in a minidomain, or nucleic acid molecules encoding the same. The library contains members with different modifications, wherein the plurality is defined by the modifications in the at least two structural loops or loop regions. The nucleic acid library preferably includes at least 10 different members (with at least two potential amino acid modifications) and more preferably includes at least 100, more preferably 1000 or 10000 different members (e.g. designed by randomisation strategies or combinatory techniques). Even more diversified individual member numbers, such as at least 1000000 or at least 10000000 are also preferred, more preferred at least 108, more preferred at least 109, more preferred at least 1010, more preferred at least 1011, up to 1012, in cases of ribosomal display even higher number are feasible.
A further aspect of the invention is the combination of two different immunoglobulins or immunoglobulin variable domains selected from at least two libraries according to the invention in order to generate multispecific immunoglobulins. These selected specific immunoglobulin variable domains may be combined with each other and with other molecules, similar to building blocks, to design the optimal arrangement of the domains to get the desired properties such as combinations of specificities and/or valencies.
Furthermore, one or more modified immunoglobulins or immunoglobulin variable domains according to the invention may be introduced at various or all the different sites of a protein without destruction of the structure of the protein. By such a “domain shuffling” technique new libraries are created which can again be selected for the desired properties.
The preferred library contains immunoglobulins or immunoglobulin variable domains according to the invention or derivatives thereof.
A preferred embodiment of the present invention is a binding molecule for an antigen (antigen binding molecule) comprising at least one immunoglobulin or immunoglobulin variable domain and at least two structural loops or loop regions being modified according to the present invention to bind to the antigen, wherein said binding molecule has no relevant and/or specific binding activity with its CDR-loops. It may comprise other parts useable for antibody activities (e.g. such as natural or modified effector regions (sequences); however, it lacks the “natural” binding region of antibodies, i.e. active CDR-loops in their naturally occurring position. These antigen binding molecules according to the present invention have the advantages described above for the present molecules, yet without the specific binding activity of antibodies; however with a newly introduced specific binding activity in the structural loop or loop region.
Also for the antigen binding molecules according to the present invention it is preferred that the new antigen binding sites in the structural loops are introduced by randomising technologies, i.e. by modifying one or more amino acid residues of at least two structural loops by randomisation techniques or by introducing randomly generated inserts into such structural loops. Alternatively preferred is the use of combinatorial approaches.
According to another aspect, the present invention relates to a modified immunoglobulin having an antigen binding site foreign to the unmodified immunoglobulin and incorporated in one, two, three or more structural loops of the immunoglobulin or immunoglobulin variable domain. In this context the term “foreign” means that the antigen binding site is not naturally formed by the specific structural loop or loop region of the variable immunoglobulin domain.
According to yet another aspect, the present invention relates to a modified immunoglobulin having an antigen binding site foreign to the unmodified immunoglobulin and incorporated in one, two, three or more structural loops of the variable domain, wherein said modified immunoglobulin binds to said antigen with an affinity of at least 103 mol−1, at least 104 mol−1, at least 105 mol−1, at least 106 mol−1, at least 107 mol−1, at least 108 mol−1, or at least 109 mol−1.
Usually binders with medium or high affinity are provided according to the invention. Those with medium affinity preferably exert a dissociation rate Kd in the range of 10−5 to 10−7, those with high affinity have a proven Kd in the range of 10−8 to 1010, those having a Kd less than 10−9 being most preferred as a high affinity binder. In some cases it will be appropriate to select binders with even lower Kd, e.g. less than 10−11, usually as low as 10−12.
Preferred immunoglobulins or immunoglobulin variable domains according to the present invention comprise at least two antigen binding sites, the first site binding to a first epitope, and the second site binding to a second epitope.
According to a preferred embodiment, the present immunoglobulin or immunoglobulin variable domain comprises at least three loops or loop regions, the first loop or loop region binding to a first epitope, and the second and third loop or loop region binding to a second epitope. Either the at least first or at least second and third loop or loop region or both may contain a structural loop. The immunoglobulin or immunoglobulin variable domains according to the present inventions include the fragments thereof known in the art to be functional which contain the essential elements according to the present invention: the structural loops or loop regions modified according to the present invention.
Preferably, the immunoglobulin according to the present invention is composed of at least two immunoglobulin domains, or a part thereof including a minidomain, and each domain contains at least one antigen binding site. One of the preferred pairs of immunoglobulin domains is a CL/CH1 pair, which may be engineered in the structural loop region that is located at the C-terminus of the CL/CH1 pair. Thereby one or two new binding sites are engineered. Upon selection of the specific CL/CH1 binding domain pair, it may be recombined with the variable domains VL and VH to obtain a Fab molecule according to the invention with one “natural” binding site in the CDR region and one or two additional binding sites opposite thereto, i.e. in the C-terminal structural loop region of the CH1/CL domains.
Thus, the immunoglobulin according to the invention may be obtained by modifying an immunoglobulin parent molecule that contains the variable domain. Alternatively, a constant immunoglobulin domain may be engineered to obtain a binding site in the structural loop region, which domain can then be used as a building block to produce combinations with variable immunoglobulin domains and optionally with other constant domains, resulting in an immunoglobulin according to the invention that contains both a variable domain and a new binding site formed by structural loops or structural loop regions.
According to such preferred embodiment of the invention there is provided an immunoglobulin, which comprises at least one domain of the variable region of an immunoglobulin and at least one domain of the constant region of an immunoglobulin; for example, a variable domain, which is modified in at least two structural loops linked to a CH1 domain.
Another aspect of the present invention relates to a kit of binding partners containing
(a) a polypeptide comprising a modified immunoglobulin variable domain having an antigen binding site incorporated in two or more structural loops, and
(b) a binding molecule containing an epitope of said antigen.
Preferably a kit of binding partners according to the invention is containing
Such a binding molecule of this kit according to the present invention may be used for selecting and distinguishing a native or modified immunoglobulin according to the present invention in a sample or from a library. It may further be used for identifying the binding specificity of polypeptides comprising a modified immunoglobulin or immunoglobulin variable domain according to the present invention. By using the binding molecule of this kit according to the present invention, the potency of the modified polypeptide according to the present invention may be determined.
Potency as defined here is the binding property of the modified molecule of the invention to its antigen. The binding can be determined quantitatively and/or qualitatively in terms of specificity and/or affinity and/or avidity by assay methods as known in the art for quality control purposes.
Moreover, the binding molecule of a kit according to the present invention may be used for selecting the polypeptide comprising a modified immunoglobulin or immunoglobulin variable domain according to the present invention from a library as specified above, preferably consisting of at least 10, preferably at least 100, more preferably at least 1000, more preferred at least 10000, especially at least 100000 polypeptides with different modifications in the structural loops.
The present invention is further illustrated by the following examples.
The crystal structure of the camel VHH domain D2-L24 in complex with Hen Egg White Lysozyme, which is published in the Brookhaven Database as entry 1ZVH.pdb was used to aid in the design of the mutated VHH domain. The sequence of chain A of the structure file 1ZVH.pdb is given in SEQ ID No. 1.
The sequence which was used as the basis for construction of the VHH library is the sequence of the anti-TNF-alpha VHH domain from patent WO04041862A21, clone 3E and is given in SEQ ID No. 2.
After detailed analysis of the structure of 1ZVH.pdb and by visual inspection of the residues forming the loops which connect the beta strands, it was decided to randomize residues 13, 15, (i.e. in the loop between beta-strands A and B) 89, 90, 92 and 93 (i.e. in the loop between beta-strands E and F) of SEQ ID No. 2 for the generation of the library. In addition, three randomized positions were decided to be inserted between residues 14 and 15, and three randomized positions were decided to be inserted between residues 92 and 93 of SEQ ID No. 2.
The engineered gene coding for the VHH sequence is produced in the form of a synthetic gene by PCR assembly. The sequence and its translation are shown in
The amino acid sequence encoded by the synthetic gene is given in SEQ ID. No.3.
The first two residues and the last two residues are caused by the restriction sites used for cloning. The nucleotide sequence coding for SEQ ID No. 3 is given in SEQ ID No. 4. SEQ ID No.4: cttgccatgg ccccccgaga accacaggtg tac
The first two codons and the last two codons are caused by the restriction sites used for cloning.
The oligonucleotides for PCR assembly of the synthetic gene are designed by use of the publicly available software tool DNAWorks 3.1 (http://helixweb.nih.gov/dnaworks/) and are assembled by PCR following standard protocols from the 18 oligos presented in Table 1 and as SEQ ID No. 5 through SEQ ID No. 22 (Hoover D M, Lubkowski J., DNAWorks: an automated method for designing oligonucleotides for PCR-based gene synthesis, Nucleic Acids Res. 2002 May 15; 30(10):e43).
Briefly, equal volumes of oligonucleotide solutions (each at a concentration of ˜1 mg/ml) are mixed together and diluted with water to a final concentration of ˜1 ng/μl for each oligonucleotide. The oligonucleotide mixture is diluted 5-fold with the PCR solution. The final concentrations of components are 0.2 ng/μl for each oligonucleotide, 20 mM for Tris-HCl (pH 8.8), 10 mM for KCl, 10 mM for (NH4)2SO4, 6 mM for MgSO4, 0.1% (v/v) for Triton X-100, 0.1 mg/ml for bovine serum albumin, 0.2 mM for each dNTP and 2.5 U for Pfu polymerase. The PCR protocol for gene assembly begins with one 5 min denaturation step of 95° C., during which the polymerase is added to avoid any possible mispriming (‘hot start’ PCR). This step is followed by 25 cycles of a denaturation temperature of 95° C. for 30 s, an annealing temperature of 55° C. for 30 s and an extension temperature of 72° C. for 1.5 min. The last step in this protocol is an incubation cycle at 72° C. for 10 min. For gene amplification, 1 μl of the mixture resulting from the gene assembly reaction are used as the template, with the outermost oligonucleotides (SEQ ID No. 5 and SEQ ID No. 22) used as primers. The PCR protocol for gene amplification is essentially the same as that for gene assembly. The assembled synthetic VHH gene is subsequently cloned via the NcoI and NotI restriction sites in the vector pET27b (Novagen, http://www.merckbiosciences.co.uk/product/69863; http://www.novagen.com) and the sequence is verified by DNA sequencing.
PCR is then used to construct the randomized library. The template for the first 2 PCR reactions is the cloned synthetic VHH gene as described above. The primer pairs used for the first two PCR reactions are as follows: 3esynmu1 (gactccatgg caagtgcaac tgcaggaaag cggaggcggt ctggttnnsc cannsnnsnn snnsggcagc ctgcgtctga get (SEQ ID No. 23)) and 3esynmu2 (catgagatct acggtgttct tggcg (SEQ ID No. 24)); 3esynmu3 (catgagatct tacgatgnns nnsttgnnsn nsnnsnnsnn sgaagatacg gcggtgtatt attg (SEQ ID No. 25)) and 3esyn2 (aatagcggcc gcagagctca cggtcacc (SEQ ID No. 26)). The resulting PCR products are digested with BglII, ligated, and the ligation product is used as template for a PCR reaction with primers 3esyn1 (acgtccatgg caagtgcaac tgcag (SEQ ID No. 27)) and 3esyn2 (aatagcggcc gcagagctca cggtcacc (SEQ ID No. 26)). The NNS codons in primers 3esynmu1 (SEQ ID No. 23) and 3esynmu3 (SEQ ID No. 25) introduce the randomized positions in the sequence. The codon NNS (IUPAC code, where S means C or G) is chosen which encodes all 20 naturally occurring amino acids, but avoids 2 out of 3 stop codons.
This randomized PCR product is subsequently cloned into the phagemid cloning vector pHEN1 (Hoogenboom H R, Griffiths A D, Johnson K S, Chiswell D J, Hudson P, Winter G. Multi-subunit proteins on the surface of filamentous phage: methodologies for displaying antibody (Fab) heavy and light chains. Nucleic Acids Res. 1991 Aug. 11; 19(15):4133-7) in frame with the pelB secretion signal via the NcoI restriction site. The NotI restriction site at the 3′ end of the gene inserts the VHH library in frame with the gene coding for the minor coat protein (protein III) of filamentous phage fd contained in the vector pHEN1. The engineered sequence of the randomized VHH library insert is given as a nucleotide sequence in SEQ ID No. 28 and translated as an amino acid sequence in SEQ ID No. 29. The Letter X in SEQ ID No. 29 denotes the randomized amino acid residues.
The ligation product is then transformed into Escherichia coli TG1, the number of obtained colonies is determined, and a number of selected clones are controlled by restriction analysis and by DNA sequencing. For the following steps of the surface display library phage preparation, standard protocols are followed. Briefly, the ligation mixture is transformed into E. coli TG1 cells by electroporation. Subsequently, phage particles are rescued from E. coli TG1 cells with helper phage M13-KO7. Phage particles are then precipitated from culture supernatant with PEG/NaCl in 2 steps, dissolved in water and used for selection by panning or, alternatively, they are stored at minus 80° C.
3 panning rounds are performed according to standard protocols. (e.g. Phage display of peptides and antibodies: a laboratory manual, Kay et al., 1996, Academic Press, San Diego, Calif.) Briefly, the following method is applied. Maxisorp 96-well plates (Nunc) are coated with HSA. 200 μl of the following solution are added per well: 0.1M Na-carbonate buffer, pH 9.6, with the following concentrations of HSA: 1st panning round: 2 mg/ml HSA; 2nd panning round: 1 mg/ml HSA; 3rd panning round: 1 mg/ml HSA Incubation is for 1 hour at 37° C., followed by blocking with 2% dry milk (M-PBS) with 200 μl per well for 1 hour at room temperature. The surface display phage library is then allowed to react with the bound HSA by adding 100 μl phage suspension and 100 μl 4% dry milk (M-PBS), followed by incubation for 45 minutes with shaking and for 90 minutes without shaking at room temperature.
Unbound phage particles are washed away as follows.
After the 1st panning round: 10×300 μl T-PBS, 5×300 μl PBS;
after the 2nd panning round: 15×300 μl T-PBS, 10×300 μl PBS;
after the 3rd panning round: 20×300 μl T-PBS, 20×300 μl PBS.
Elution of bound phage particles is performed by adding 200 μl per well of 0.1 M glycine, pH 2.2, and incubation with shaking for 30 minutes at room temperature. Subsequently, the phage suspension is neutralized by addition of 60 μl 2M Tris-Base, followed by infection into E. coli TG1 cells by mixing 10 ml exponentially growing culture with 0.5 ml eluted phage and incubation for 30 minutes at 37° C. Finally, infected bacteria are plated on TYE medium with 1% glucose and 100 μg/ml ampicillin, and incubated at 30° C. overnight.
Phagemid DNA from the phage selected through the 3 panning rounds is isolated with a midi-prep. DNA encoding mutated VHH domains regions is batch-amplified by PCR and cloned NcoI-NotI into the vector pNOTBAD/Myc-His, which is the E. coli expression vector pBAD/Myc-His (Invitrogen) with an inserted NotI restriction site to facilitate cloning. Ligated constructs are transformed into E. coli LMG194 cells (Invitrogen) with electroporation, and grown at 30° C. on TYE medium with 1% glucose and ampicillin overnight. Selected clones are inoculated into 200 μl 2xYT medium with ampicillin, grown overnight at 30° C., and induced by adding L-arabinose to an end concentration of 0.1%. After expression at 16° C. overnight, the cells are harvested by centrifugation and treated with 100 μl Na-borate buffer, pH 8.0, at 4° C. overnight for preparation of periplasmic extracts. 50 μl of the periplasmic extracts are used in ELISA (see below).
The periplasmatic extracts of the VHH mutants selected for human serum albumin-binding are tested in an ELISA with the following protocol:
Coating: Microtiter plate (NUNC, Maxisorp), 100 μl per well, 100 μg HSA/ml in PBS, overnight at 4° C.
Wash: 3×200 μl PBS
Blocking: 1% Blocker Casein in PBS (Pierce), 1 h at RT
Wash: 3×200 μl PBS
Periplasmic extract binding: 50 μl periplasmic extract (Example 4), 50 μl PBS 0.05% Tween 20, at room temperature overnight Wash: 3×200 μl PBS
1st antibody: anti-His4 (Qiagen), 1:1000 in PBS 0.05% Tween 20, 90 min at RT, 100 μl per well
Wash: 3×200 μl PBS
2nd antibody: goat anti mouse*HRP (SIGMA), 1:1000 in PBS 0.05% Tween 20, 90 min at RT (room temperature), 100 μl per well
Wash: 3×200 μl PBS
Detection: 3 mg/ml OPD in Na-citrate/phosphate buffer, pH 4.5, 0.4 μl 30% H2O2
Stopping before background gets too high: 100 ml 3M H2SO4
Absorbance read: 492/620 nm
The synthetic gene coding for the engineered VHH gene described above in example 2 is used as a template for two PCR reactions in which the following primer pairs are used: SEQ ID No. 30 (actgctcgag agacatcgcc aagaacac; esynmu4) together with SEQ ID No. 26 (3esyn2) and SEQ ID No. 31 (cacactcgag atcgcaaasn nsnnsnncac snnsnncgca tagtaggtat tgcc; 3esynmu5) together with SEQ ID No. 27 (3esyn1). The resulting PCR products are digested with XhoI, ligated, and the ligation product is used as template for a PCR reaction with primers 3esyn1 (SEQ ID No. 27) and 3esyn2 (SEQ ID No. 26). The NNS codons in primers 3esynmu4 (SEQ ID No. 30) and 3esynmu5 (SEQ ID No. 31) introduce the randomized positions in the sequence similarily as described in example 2.
This randomized PCR product is subsequently cloned into the phagemid cloning vector pHEN1 (Hoogenboom H R, Griffiths A D, Johnson K S, Chiswell D J, Hudson P, Winter G. Multi-subunit proteins on the surface of filamentous phage: methodologies for displaying antibody (Fab) heavy and light chains. Nucleic Acids Res. 1991 Aug. 11; 19(15):4133-7) in frame with the pelB secretion signal and the minor coat protein (protein III) of filamentous phage fd contained in the vector pHEN1 as described in example 2. The engineered sequence of the randomized VHH library insert is given as a nucleotide sequence in SEQ ID No. 32 and translated as an amino acid sequence in SEQ ID No. 33. The Letter X in SEQ ID No. 33 denotes the randomized amino acid residues.
The ligation product is then transformed into Escherichia coli TG1, the number of obtained colonies is determined, and a number of selected clones are controlled by restriction analysis and by DNA sequencing. For the following steps of the surface display library phage preparation, standard protocols are followed as described in example 2. The steps of panning, selection and characterization of specifically binding clones are performed essentially as described in examples 3, 4 and 5.
The library with randomized residues in the AB loop and in the EF loop as described in example 2 is used as a template for a PCR in which the same primer pairs as in example 6 are used: SEQ ID No. 30 (esynmu4) together with SEQ ID No. 26 (3esyn2) and SEQ ID No. 31 (3esynmu5) together with SEQ ID No. 27 (3esyn1). The following steps for library construction, cloning, panning, selection and characterization of specifically binding clones are essentially as described in examples 2, 3, 4 and 5.
The libraries are used in panning with various antigens.
3 panning rounds are performed. Maxisorp 96-well plates (Nunc) are coated with hen egg lysozyme by adding 200 μl of the following solution per well:
PBS, with the following concentrations of dissolved hen egg lysozyme (HEL):
1st panning round: 2 mg/ml HEL
2nd panning round: 1 mg/ml HEL
3rd panning round: 1 mg/ml HEL
Incubation is for 1 hour at 37° C., followed by blocking with 2% dry milk (M-PBS) with 200 μl per well for 1 hour at room temperature.
The surface display phage library is then allowed to react with the bound hen egg lysozyme by adding 100 μl phage suspension and 100 μl 4% dry milk (M-PBS), followed by incubation for 45 minutes with shaking and for 90 minutes without shaking at room temperature.
Unbound phage particles were washed away as follows:
1st panning round: 10×300 μl T-PBS, 5×300 μl PBS
2nd panning round: 15×300 μl T-PBS, 10×300 μl PBS
3rd panning round: 20×300 μl T-PBS, 20×300 μl PBS
Elution of bound phage particles is performed by adding 200 μl per well of 0.1 M glycine, pH 2.2, and incubation with shaking for 30 minutes at room temperature. Subsequently, the phage suspension is neutralized by addition of 60 μl 2M Tris-Base, followed by infection into E. coli TG1 cells by mixture of 10 ml exponentially growing culture with 0.5 ml eluted phage and incubation for 30 minutes at 37° C. Finally, infected bacteria are plated on TYE medium with 1% glucose and 100 μg/ml Ampicillin, and incubated at 30° C. overnight.
The libraries of examples 2, 6 and 7 are used in panning rounds as described above. Specifically, the phage libraries are suspended in binding buffer (PBS, 1% ovalbumin, 0.005% Tween 20) and panned against human serum albumin immobilized directly on maxisorp plates (10 micrograms/ml in PBS, overnight at 4° C.; plates are blocked with Blocker Casein (Pierce). After 2 hours, unbound phages are removed by repetitive washing (PBS, 0.05% Tween 20) and bound phage are eluted with 500 mM KCl, 10 mM HCl, pH2.
After each HSA-specific panning round the resulting clones are selected or tested for binding to TNF alpha. Selection and testing for TNF-alpha specificity is performed as described in example 1 of WO2004/041862.
The panning is performed as described in WO02060919, Example 6.2. In short, phage libraries are resuspended in 5 ml 20 mM MES, pH 6.0/5% skimmed milk/0.05% Tween 20 and added (100 microlitre of 5×1012 PFU/ml/well) to 20 wells of a Maxisorp immunoplate (Nunc) previously coated with 1 microgram of murine FcRn and blocked with 5% skimmed milk. After incubation for 2 h at 37° C., wells are washed 10-30 times with 20 mM MES, pH 6.0/0.2% Tween 20/0.3 M NaCl and phage eluted by incubation in 100 microlitre PBS, pH 7.4/well for 30 min at 37° C. Phages are used to reinfect exponentially growing E. coli TG1, as described in example 3.
After each panning round on FcRn the resulting clones are selected or tested for binding to TNF alpha as described above.
Panning against recombinant fusion proteins of Fc-gammaRI, Fc-gammaRIIA and Fc-gammaRIIA are performed as described in Berntzen et al (2006) Protein Eng Des Sel 19:121-128 After each panning round on an Fc-receptor the resulting clones are selected or tested for binding to TNF alpha as described above.
This example demonstrates the possibility to introduce new functions or additional binding specificities into an antibody fragment. The molecule used as a starting point for modification is the murine single chain antibody fragment sFv 26-10 (Huston et al. (1988) Proc Natl Acad Sci USA. 85:5879-5883).
Five different libraries are constructed to modify different structural loop sequences by random amino acid sequences:
The respective genes are assembled with chemically synthesized oligonucleotides and cloned in a phage display vector for phage surface display as described above with all necessary adaptions to achieve in-frame translation of a leader peptide, the sFv-variant and the coat protein III of the phage.
The phage displayed libraries are selected for binding to human serum albumine, lysozyme, FcRn and Fc gamma receptors as described in example 8.
Alternatively the genes are ligated with the vector pRDV analog to the method described in Binz et al. (2005) Nat Biotechnol. 22:575-582 and panned for human serum albumine, Fc-receptors and lysozyme according to the methodology described in Schaffitzel et al. (1999) J Immunol Methods 231:119-135.
A human antibody, 2F5, specific for the HIV-peptide ELDKWA is used as a scaffold for randomization of structural loops and expressed as scFv. Expression and Phage display vector construction is performed as described in example 9. Phage selection is performed accordingly.
The wild type scFv sequence and the respective libraries are shown in
For the selection of specifically binding molecules from libraries of immunoglobulin domains, in which residues that are located in structural loops have been randomized, various formats can be applied. Single domains, such as VL, VH, CH1, CH2, CH3, CH4 or CL domains can be used, Fc fragments which consist of CH2 and CH3 domains (including or not including the hinge region or parts thereof) can be used, Fv or single-chain Fv fragments can be used, whole antibodies can be used or other combinations of immunoglobulin domains can be used. One format that is of particular interest for the selection of specifically binding molecules is the Fab fragment, which is a heterodimer of two chains, namely the VL-CL part and the VH-CH1 part of the antibody. Fab fragments have been known for a long time, and can be produced by proteolytic cleavage of an IgG with the protease papain, and they can also be produced recombinantly in a wide range of different expression systems, such as for example Escherichia coli, Saccharomyces cerevisiae, Pichia pastoris, insect cells or mammalian cells.
It is well known in the art that surface display systems, such as phage display, yeast display, and other systems such as ribosome display etc. can be used for the enrichment and selection of specifically binding molecules such as Fab fragments from large libraries (See for example Hoogenboom H R, Griffiths A D, Johnson K S, Chiswell D J. Hudson P, Winter G.
Multi-subunit proteins on the surface of filamentous phage: methodologies for displaying antibody (Fab) heavy and light chains. Nucleic Acids Res. 1991 Aug. 11; 19(15):4133-7.; Kang A S, Barbas C F, Janda K D, Benkovic S J, Lerner R A. Linkage of recognition and replichtion functions by assembling combinatorial antibody Fab libraries along phage surfaces. Proc Natl Acad Sci USA. 1991 May 15; 88(10):4363-6.; Kang X, Yang B A, Hu Y, Zhao H, Xiong W, Yang Y, Si B, Zhu Q. Human neutralizing Fab molecules against severe acute respiratory syndrome coronavirus generated by phage display. Clin Vaccine Immunol. 2006 August; 13(8):953-7.; Weaver-Feldhaus J M, Lou J, Coleman J R, Siegel R W, Marks J D, Feldhaus M J. Yeast mating for combinatorial Fab library generation and surface display. FEBS Lett. 2004 Apr. 23; 564(1-2):24-34.).
As an example, if the phage display system is applied for the display of Fab fragments (e.g. libraries of Fab fragments), one chain of the Fab fragment, e.g. the VH-CH1 chain, can be expressed as a fusion protein with e.g. protein III of phage M13, thereby leading to the display of this chain on the phage surface, while the other chain, VL-CL, is expressed in soluble form and forms the natural heterodimer with the surface anchored VH-CH1 chain. In a typical Fab surface display library, different VH and VL sequences are present, which can originate from a donor, typically a mouse or a human, but diversity can also be generated by in vitro methods such as site directed mutagenesis. Different binding sites are thereby generated, and by the use of a suitable display or other enrichment or selection method specifically binding clones can be isolated from such libraries that bind to their binding partner via the binding site that is formed by VH and VL.
Fab fragments can be generated that bind to one target via their natural binding site formed by VH and VL, and to another (or a second time to the same) target via binding sites formed by their structural loops. In order to obtain such engineered Fab fragments, libraries of Fabs are first generated in which residues in the structural loops are replaced by randomized sequences. Insertions of additional residues can also be made. Structural loops that can be engineered by this approach can be either C-terminal loops (the “bottom” loops) of VH or VL, or N-terminal (“top” loops) or C-terminal (“bottom” loops) of the CH1 or of the CL domains. Different combinations of domains with engineered structural loops at any of these positions are also possible. One format that can be used to select specifically binding domains is as single domains, as Fv or single-chain Fv fragments, or, as described in detail below, as Fab fragments.
The genes coding for VH-CH1 and VL-CL respectively of the antibody 4D5 (Cho H S, Mason K, Ramyar K X, Stanley A M, Gabelli S B, Denney D W Jr, Leahy D J. Structure of the extracellular region of HER2 alone and in complex with the Herceptin Fab. Nature. 2003 Feb. 13; 421(6924):756-60.), which binds to human Her2 are used for this example. A synthetic gene is constructed which consists of the 4D5 VL-CL encoding part of the gene, flanked at its 5′ end by an NcoI site for in-frame insertion in the pelB signal sequence contained in the phagemid vector pHEN1 (Hoogenboom H R, Griffiths A D, Johnson K S, Chiswell D J, Hudson P, Winter G. Multi-subunit proteins on the surface of filamentous phage: methodologies for displaying antibody (Fab) heavy and light chains. Nucleic Acids Res. 1991 Aug. 11; 19(15):4133-7) followed by a stop codon. At the transit of the sequence from VL into CL, a unique BsiWI restriction site is included, which is used later on for replacement of the wildtype CL sequence against library inserts containing randomized structural loops in combination with a unique AscI restriction site that is located downstream of the stop codon of the VL-CL encoding gene. It follows a sequence which contains a ribomsome binding site (Shine-Dalgarno sequence) taken from Carter et al. (Carter P. Kelley R F, Rodrigues M L, Snedecor B, Covarrubias M, Velligan M D, Wong W L, Rowland A M, Kotts C E, Carver M E, et al. High level Escherichia coli expression and production of a bivalent humanized antibody fragment. Biotechnology (N Y). 1992 February; 10(2):163-7), followed by a gene segment encoding the heat stable enterotoxin II (stII) signal sequence fused in frame to the VH-CH1 encoding part of the antibody 4D5 followed by a NotI site for in-frame insertion in the vector pHEN1. This dicistronic construct leads to the expression of VL-CL (the protein sequence of which is given in SEQ ID No. 44) on the one hand an on the other hand of VH-CH1 fused to protein III of phage M13 (the protein sequence of which is given in SEQ ID No. 45), which is encoded by pHEN1. The complete sequence of the 4D5 Fab display vector as described here is given as a nucleotide sequence in SEQ ID No. 46.
For construction of a library of CL domains in which residues in the structural loops are randomized, a synthetic gene is made which encodes a human kappa constant domain (CL) in which certain codons are replaced by a degenerated codon such as for example NNB (IUPAC code, where N stands for C, G, T and A; B stands for T, C and G). It is also possible to insert additional residues into the sequence. In this example, 3, 4 or 5 residues respectively are inserted between residues 127 and 128, and residues 182-185 and 187-189 are randomized (Kabat numbering). The sequences of the resulting genes are given as nucleotide sequences in SEQ ID No. 47, 48, and 49 (3, 4 or 5 insertions respectively between residues 127 and 128) and as amino acid sequences in SEQ ID No. 50, 51 and 52 (the letter X stands for any of the 20 naturally encoded amino acids). The nucleotide sequences include the BsiWI site on the 5′ end and the AscI site at the 3′ end for cloning into SEQ ID No. 46.
To construct the phage display library, the Fab 4D5 display vector (SEQ ID No. 46) is cleaved with the restriction enzymes BsiWI and AscI, and the large fragment is prepared by preparative agarose gel electrophoresis. The small fragment, corresponding to the gene encoding the wildtype CL is removed. The mixture of library inserts as described above (SEQ ID Nos. 47-49) and likewise cleaved with BsiWI and AscI and ligated to the purified vector fragment. The ligation mixture is transformed into a suitable E. coli strain such as TG1 by e.g. electroporation, and a large number of independent colonies are generated (e.g. 10exp8, 10exp9 or more). The transformed bacteria are pooled and infected with helper phage (such as e.g. M13K07) for rescue of phage particles. The phage particles are produced by standard procedures and used for panning of the library.
Panning of the library against a given target yields Fab fragments that not only bind to Her2 (due to binding site formed by VH and VL of the antibody 4D5) but also to the target against which they were selected.
In this example, the design, preparation and use of a Fab display library, in which structural loops of the CL domain are modified, is described. In an analogous way, libraries with randomization in the structural loops of other domains, such as the CH1, the VH or the VL domain can be prepared and used.
| Number | Date | Country | Kind |
|---|---|---|---|
| A 1145/2006 | Jul 2006 | AT | national |
This application is a continuation of U.S. application Ser. No. 12/307,569, filed Sep. 21, 2009, which is a 371 national phase filing of PCT/AT2007/000343, filed Jul. 5, 2007, which claims the benefit of Austria A 1145/2006, filed Jul. 5, 2006, the contents of each of which are incorporated herein by reference in their entirety.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 12307569 | Sep 2009 | US |
| Child | 14853919 | US |
