Multivalent antigen-binding proteins

FIELD OF THE INVENTION

The present invention relates to multivalent and multispecific antigen binding proteins, methods for their production and uses thereof. In particular, the invention relates to antigen binding proteins comprising a polypeptide comprising in series two or more single domain binding units which are preferably variable domains of a heavy chain derived from an immunoglobulin naturally devoid of light chains.

BACKGROUND OF THE INVENTION

Antibodies are protein molecules belonging to a group of immunoglobulins generated by the immune system in response to an antigen. The structure of most antibody molecules is based on a unit comprising four polypeptides, two identical heavy chains and two identical light chains, which are covalently linked together by disulphide bonds. Each of these chains is folded in discrete domains. The C-terminal regions of both heavy and light chains are conserved in sequence and are called the constant regions, comprising one or more so-called C-domains. The N-terminal regions of the heavy and light chains, also known as V-domains, are variable in sequence and determine the specificity of the antibody. The regions in the variable domains of the light and heavy chains (V

L

and V

H

respectively) responsible for antigen binding activity are known as the hypervariable or complementarity determining regions (CDR).

Natural antibodies generally have at least two identical antigen-binding sites defined by the association of the heavy and light chain variable regions. Individual heavy or light chain domains having the capability to bind antigens have been described in the literature (Ward et al, Nature 341 (1989), 544-546) although generally most naturally occurring antibodies need both a V

H

and V

L

to form a complete antigen binding site and retain full immunoreactivity.

More recently, immunoglobulins capable of exhibiting the functional properties of the four-chain immunoglobulins described above but which comprise two heavy polypeptide chains and which furthermore are devoid of light polypeptide chains have been described (see European Patent Application EP-A-0584421, Casterman et al, 1994). Methods for the preparation of such antibodies or fragments thereof on a large scale comprising transforming a mould or yeast with an expressible DNA sequence encoding the antibody or fragment are described in patent application WO 94/25591 (Unilever).

The immunoglobulins described in EP-A-0584421, which may be isolated from the serum of Camelids, do not rely upon the association of heavy and light chain variable domains for the formation of the antigen-binding site but instead the heavy polypeptide chains alone naturally form the complete antigen binding site. These immunoglobulins, hereinafter referred to as “heavy-chain immunoglobulins” are thus quite distinct from the heavy chains obtained by the degradation of common (four-chain) immunoglobulins or by direct cloning which contribute part only of the antigen-binding site and require a light chain partner for antigen-binding, thus forming a complete antigen binding site.

As described in EP-A-0584421, heavy chain immunoglobulin V

H

regions isolated from Camelids (forming a complete antigen binding site and thus constituting a single domain binding site) differ from the V

H

regions derived from conventional four-chain immunoglobulins in a number of respects, notably in that they have no requirement for special features for facilitating interaction with corresponding light chain domains. Thus, whereas in common (four-chain) immunoglobulins the amino acid residues at the positions involved in the V

H

/V

L

interaction is highly conserved and generally apolar leucine, in Camelid derived V

H

domains this is replaced by a charged amino acid, generally arginine. It is thought that the presence of charged amino acids at this position contributes to increasing the solubility of the camelid derived V

H

. A further difference which has been noted is that one of the CDRs of the heavy chain immunoglobulins of EP-A-0584421, the CDR

3

, may contain an additional cysteine residue associated with a further additional cysteine residue elsewhere in the variable domain. It has been suggested that the establishment of a disulphide bond between the CDR

3

and the remaining regions of the variable domain could be important in binding antigens and may compensate for the absence of light chains.

In the search for multivalent and multispecific antigen binding proteins, attention has been directed towards the use of fragments, or portions, of a whole antibody which can nevertheless exhibit antigen binding activity. By comparison with the whole antibody, the smaller antibody fragment is advantageous for use in therapy, for example, as it is likely to be less immunogenic and more able to penetrate tissue.

Binding fragments of common (four-chain) antibodies which have been considered include Fab (light chain associated with the V

H

and C

H1

domains of a heavy chain), F

V

(comprising of the V-domains of the heavy and light chains associated with each other) and ScFv (comprising a V

H

domain linked to a V

L

domain by a flexible peptide linker) fragments. These fragments have only one site for antigen binding compared to the two or more sites contained in the whole antibody, however, and in an attempt to overcome this problem, recombinant fragments having two or more binding sites have been proposed.

In general, those multivalent and/or multispecific constructions which have been described in the literature either comprise two or more polypeptide chains, see for example, patent application WO 94/09131 (Scotgen Limited) and WO 97/14719 (Unilever) or are based on a ‘double ScFv’ approach, wherein the multivalency arises when two or more monovalent ScFv molecules are linked together, providing a single chain molecule comprising at least four variable domains, as described, for example, in WO 93/11161 (Enzon Inc) and WO 94/13806 (Dow Chemical Co). In all of these cases, the binding site is formed through the association of light and heavy chain variable domains. In WO 93/11161, reference is made to a single-chain protein comprising the binding portions of the variable regions of an antibody light (or heavy) chain but it is stated that as such proteins are comprised of two similar variable regions, they do not necessarily have any antigen-binding capability.

EP-A-0584421 (Casterman), referred to above, discloses fragments of heavy chain immunoglobulins devoid of light chains, including fragments corresponding to isolated V

H

domains or to V

H

dimers linked by the hinge disulphide. Further disclosed, but not exemplified, are antibodies having different specificities on each heavy polypeptide chain which could be prepared by combining two heavy chain immunoglobulins or one heavy chain of an immunoglobulin of EP-A-0584421 with a fragment of a conventional four-chain immunoglobulin. There is no suggestion that multivalent and/or multispecific constructs may be prepared by joining together individual V

H

domains. Indeed, in the absence of the inherent conformational constraints conferred on the position of the binding sites by the presence of a corresponding light chain, it might generally be expected that the binding domains in constructs of this type would sterically hinder each other, unfavourably influencing binding activity.

SUMMARY OF THE INVENTION

In a first aspect, the invention provides a multivalent antigen binding protein comprising a single polypeptide chain comprising, connected in series, two or more single domain binding units.

In another aspect, the invention provides nucleotide sequences coding for multivalent antigen binding proteins according to the invention and cloning and expression vectors comprising such nucleotide sequences. Further provided are host cells transformed with vectors comprising such nucleotide sequences and methods of producing antigen binding proteins according to the invention by expression of the nucleotide sequences in such hosts.

The invention also provides compositions comprising multivalent antigen binding proteins according to the invention.

In a further aspect, the invention provides the use of multivalent antigen binding proteins as set forth above in diagnosis or therapy or in other methods for which antibodies or fragments thereof can be used, such as in immunoassay or purification methods. Methods of treatment using the multivalent antigen binding proteins according to the invention are also provided.

In a particular embodiment of the invention, there is provided the use of said multivalent antigen binding proteins in inactivating (bacterio)phages.

By means of the invention, antigen binding proteins having the specificity and binding affinity of the whole immunoglobulin but which have the additional advantage of smaller size are obtained. Furthermore, where the multivalent antigen binding proteins of the present invention comprise variable domains having different antigen specificity, multispecific binding molecules may be obtained. Another advantage is that the constructs according to the invention may conveniently be produced at high yields economically and efficiently on a scale appropriate for industrial use.

The present invention may be more fully understood with reference to the following description, when read together with the accompanying drawings. For convenience, an antigen binding protein according to the invention comprising two single binding units is herein referred to as a ‘bihead’.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1

shows a schematic representation of Camelidae IgG types.

FIG. 2

shows the nucleotide sequence of the PstI-BstEII insert of plasmid pUR4638, encoding the heavy chain variable domain of an anti-RR6 antibody (denoted R7) from a llama.

FIG. 3

shows the nucleotide sequence of the PstI-BstEII insert of plasmid pUR4640, encoding the heavy chain variable domain of another anti-RR6 antibody (denoted R9) from a llama.

FIG. 4

shows the nucleotide sequence of the PstI-BstEII insert of plasmid pUR4601, encoding the heavy chain variable domain of an anti-hCG antibody (denoted H14) from a llama.

FIG. 5

shows the nucleotide sequence of the PstI-BstEII insert of plasmid pUR4602, encoding the heavy chain variable domain or another anti-hCG antibody (denoted HI-15) form a llama.

FIG. 6

shows the nucleotide sequence of the PstI-BstEII insert of plasmid pUR4603, encoding the heavy chain variable domain of an anti-Streptococcus antibody (denoted S36) from a llama.

FIG. 7

shows the nucleotide sequence of the PstI-BstEII insert of plasmid pUR4642, encoding the heavy chain variable domain of another anti-Streptococcus antibody (denoted S120) from a llama.

FIG. 8

shows a map of plasmid pUR4619.

FIG. 9

shows the nucleotide sequence within plasmid pUR4619, which encodes an anti-hCG-anti-RR6 bispecific biheaded antigen binding protein (denoted H14-R9), missing the first 4 and last 3 amino acids.

FIG. 10

shows the nucleotide sequence within plasmid pUR4620, which encodes an anti-hCG-anti-RR6 bispecific biheaded antigen binding protein (denoted HI15-R7), missing the first 4 and last 3 amino acids.

FIG. 11

shows the nucleotide sequence within plasmid pUR4621, which encodes an anti-hCG-anti-RR6 bispecific biheaded antigen binding protein (denoted HI15-R9), missing the first 4 and last 3 amino acids.

FIG. 12

shows the nucleotide sequence within plasmid pUR4622, which encodes a homodimeric bivalent anti-RR6 antigen binding protein (denoted R7—R7), missing the first 4 and last 3 amino acids.

FIG. 13

shows the nucleotide sequence within plasmid pUR4623, which encodes a heterodimeric bivalent anti-RR6 antigen binding protein (denoted R7-R9).

FIG. 14

shows the results of an hCG/RR-6 bispecific binding assay.

FIG. 15

shows the results of a RR6/RR6 bifunctional binding assay.

FIG. 16

shows the binding activity and SDS-PAGE analysis of crude

P. Pastoris

supernatants expressing the constructs of Example 4.

FIG. 17

shows a plasmid map of pHP14.3A.

FIG. 18

shows the binding activity and SDS-PAGE analysis of crude

H. polymorpha

supernatants expressing the constructs of Example 5.

FIG. 19

shows the reduction of infectivity of lactic acid bacteria phages using the constructs according to the invention.

FIG. 20

shows a diagrammatic representation of the use of a biheaded antibody to form an active binding layer.

FIG. 21

shows the capture of I

125

labelled hCG to antibody adsorbed and double headed antibody fragment sensitised RR6-BSA wells.

FIG. 22

shows a schematic representation of the use of a bispecific biheaded antibody fragment of the invention in an immunoassay to detect hCG antigen.

FIG. 23

shows the assay response of latex made by adsorption of a monoclonal antibody and self-assembled bihead/RR6-BSA latex.

FIG. 24

shows the assembly of a bispecific antibody fragment on a dextran surface coated with RR6-BSA.

FIG. 25

shows acidification curves of milk by the lactic acid bacterium

Lactococcus lactis

subsp.

cremoris

LM0230 with and without phage P2 and/or bihead 3850 (also referred to as bihead 3-2).

FIG. 26

shows the A405 signals of an ELISA to determine bispecificity of H14-R9 biheads A405.

FIG. 27

shows the nucleotide sequence within plasmid pUR4618 which encodes an anti-hcg anti-RR6 bispecific biheaded antigen binding protein (denoted H14-R7, missing the first 4 and last 3 amino acids.

DETAILED DESCRIPTION OF THE INVENTION

The invention is based on the finding that the variable domains of a heavy chain derived from an immunoglobulin naturally devoid of light chains may be joined together to form a multivalent single polypeptide which retains the antigen binding affinity of the parent whole immunoglobulin but which is much smaller in size and therefore less immunogenic, thereby providing important benefits over the use of whole antibody molecules, particularly, for example, in the area of diagnostics, therapy and targeting. Accordingly, the invention as described herein is directed to multivalent forms of antigen binding proteins, methods for preparing them and new and improved methods for their use.

As used herein, a multivalent antigen binding protein is a protein which has more than one antigen binding site.

Included within this are bivalent, trivalent, tetravalent and so on. According to one aspect, bivalent forms, that is forms having two antigen-binding sites, are preferred but it will be appreciated that higher multivalent forms may find application in certain circumstances.

A single domain binding unit means an immunoglobulin variable domain which naturally forms a complete antigen binding site.

The single domain binding units for use according to the present invention are preferably heavy chain variable domains derived from any immunoglobulin naturally devoid of light chains, such that the antigen-binding site is located exclusively in the heavy chain variable domain. Preferably, the heavy chain variable domains for use in the invention are derived from immunoglobulins naturally devoid of light chains such as may be obtained from camelids as described in EP-A-0584421, discussed above.

Where the individual single domain binding units which are joined together to form the multivalent antigen binding proteins of the invention have the same antigen specificity, a binding protein which binds more than one molecule of the same type will be produced. Alternatively, multivalent and multispecific binding proteins according to the invention which are able to bind different epitopes from each other may be obtained by assembling together single domain binding units directed against different antigens. Heavy chain variable domains derived from an immunoglobulin naturally devoid of light chains having a determined antigen specificity may conveniently be obtained by screening expression libraries of cloned fragments of genes encoding camelid immunoglobulins generated using conventional techniques, as described, for example, in EP-A-0584421 and Example 1.

The multivalent antigen-binding proteins of the invention may be formed by linking together the single domain binding units in series, such that each single domain binding unit is linked to at least one other variable domain.

The individual single domain binding unit may be linked sequentially by means of peptide linkers, conveniently flexible peptide linkers which allow the domains to flex in relation to each other such that simultaneous binding to multiple antigenic determinants may be achieved. It will be appreciated that the binding of the linker to the individual single domain binding unit will be such that it does not affect the binding capacity of the single domain antigen binding site. Any peptide linker which permits the single domain binding units components to be linked in such a way that each variable domain retains the binding specificity of the whole immunoglobulin from which it is derived may suitably be used. Such linkers include, e.g., peptides derived from known proteins, such as glucoamylase, cellobiohydrolase, or cell wall proteins (CWP), or synthetic peptides which are rationally designed. The linker may suitably comprise from 1 to 400 or more amino acid residues; conveniently, the peptide linker comprises from 5 to 20 amino acid residues. This group of antigen binding proteins according to the invention with such a linker between the two single domain binding units is usually preferred because of its good production yields.

In another preferred embodiment of the invention, the individual single domain binding units may be connected directly in series without any intervening linker. In this way, the binding sites in the multivalent binding proteins according to the invention are held in much closer proximity to each other than would be the case in the whole immunoglobulin from which the immunoglobulin fragments are derived. It might generally be expected that this would give rise to unfavourable steric interactions, but surprisingly, full binding activity is found to be retained. Furthermore, these fragments with directly linked single domain binding units appear to be more stable, e.g. towards proteolytic degradation.

In an alternative embodiment, functional groups such as enzymes may be fused to the antigen binding protein.

The multivalent antigen binding proteins according to the invention may suitably find application in a wide variety of uses for which antibodies, or fragments thereof, have been proposed in the art. These uses include diagnosis, therapy, targeting, immunoassays, in agglutination, agglutination assays and purification processes, and detergents.

For use in diagnosis or therapy targeting, antigen binding proteins according to the invention having binding activity directed against both target site and the diagnostic or therapeutic agent may be constructed. Multivalent binding proteins having two or more distinct binding specificities are of particular use, for example, in the targeted delivery of therapeutic agents to their intended site of action. The binding proteins according to the invention establish the connection between therapeutic agent and target site by self-assembly, thereby avoiding the need for chemical conjugation reactions, and the therapeutic agent is guided to the target, giving increased local efficiency. Cytotoxic agents may be targeted directly to the tumour cell to be attacked, for example, by means of a bispecific, bivalent binding protein according to the invention having specificity for both the cell and the cytotoxic agent. Enzymes which are capable of generating a cytotoxic product at a target site, particularly oxido-reductases such as glucose oxidase (which catalyses the oxidation of glucose to gluconic acid, thereby producing hydrogen peroxide which exhibits cell toxicity) similarly can conveniently be delivered to the intended site of action using a binding protein according to the invention having both anti-target and anti-enzyme specificity.

Alternatively, the antigen binding proteins according to the invention may conveniently be attached to one or more appropriate diagnostically or therapeutically effective agents or carriers by methods conventional in the art.

Direct attachment of the diagnostically or therapeutically effective agent to the small antigen binding proteins of the invention runs the risk that the binding activity will be adversely affected through steric hindrance of the binding site. In a particular embodiment, therefore, the antigen binding protein has an additional polypeptide group appended to it, which additional polypeptide group does not contribute to the binding properties but which provides a “handle” for the attachment of the diagnostic or therapeutic agent.

Such antigen binding proteins with an attached polypeptide also find particular application in immunoadsorption processes, especially immunoaffinity purification processes which require that the binding protein be linked to another material, for example a label, such as an enzyme, or a solid phase, for example, a carrier material in a column.

The additional peptide group is generally attached to the antigen binding protein at or near one end of its polypeptide chain through a peptide bond, such that this polypeptide chain is prolonged by the additional peptide which now forms the terminal portion of the chain. Conveniently, the additional peptide group will be attached at its amino terminus. Suitable additional peptide linking groups and methods for their attachment are described in WO 91/08492 (Unilever). Conveniently, they comprise at least 5 but preferably not more than 20 amino acid residues and preferably include at least one lysine residue as this provides a convenient site for covalent attachment onto surfaces or proteinaceous tracers such as enzymes. A particularly suitable additional peptide linking group, particularly for coupling the antigen binding protein to a solid plastics surface, comprises the “Myc” amino acid sequence:

GLU-GLN-LYS-LEU-ILE-SER-GLU-GLU-ASP-LEU-ASN. (see SEQ ID. NO: 1)

Coupling of the additional peptide to a solid surface such as latex particles and other structures formed from plastics material commonly used in immunoassays may conveniently be achieved by means of conventional chemical cross-linking agents. It will be appreciated that the chemical coupling site in the additional peptide should preferably be sufficiently remote from the variable domain binding sites such that the coupled molecule does not affect binding activity. Alternatively, therapeutic agents and tracers such as enzymes (for example horse radish peroxidase, alkaline phosphatase, glucose oxidase) may be covalently coupled to the additional peptide via the E-amino (epsilon)group of the lysine group.

Multivalent, multispecific binding proteins according to the invention may be used to particular advantage in adsorption and purification techniques by value of their ability to exhibit specificity for two or more distinct materials. The detection and purification of ligands may conveniently be achieved using surfaces activated with constructs according to the invention. By way of illustration, a suitable support incorporating molecules for which a binding protein according to the invention has binding specificity can be activated or sensitised by coating it with a bispecific binding protein of appropriate binding specificity, the remaining binding specificity being free to bind with analyte or contaminant as appropriate depending on the intended use. Suitable molecules which can be incorporated into the support, either by adsorption or covalent bonding, include proteins, peptides, carbohydrates, DNA, RNA or conjugates thereof. Particularly preferred ligands which may be detected or purified in this way include human chorionic gonadotrophin, luteinising hormone, estrone, progesterone or metabolites thereof. The support may be particulate, planar or porous in nature. Suitable supports include those conventionally used in immuno-adsorption and purification techniques, particularly latex particles, polystyrene wells and dextran surfaces.

In an alternative aspect, binding proteins according to the invention may be used as cross-linking reagents. For example, a bispecific binding protein can link one phage to another, thereby leading to their inactivation. Inactivation of viruses or microorganisms may similarly be accomplished through agglutination.

In a further embodiment of the invention, binding proteins may be used in detergent compositions, and the like, for the treatment of stains essentially as described in PCT/EP 98/03438. Thus, for example, a bispecific protein according to the invention can have high binding affinity for stain as one specificity and for enzyme as another one. Such a bispecific protein could fulfil the requirement of accumulating enzyme on stain either by supplying said protein together with enzyme as a pre-formed non-covalent complex or by supplying the two separately and allowing them to self-assemble either in the wash liquor or on the stain. A further important aspect is to use a binding protein that binds to several different, but structurally-related, molecules in a class of “stain substances”. This would have the advantage of enabling a single enzyme species to bind (and bleach) several different stains. An example would be to use a binding protein which binds to the polyphenols in wine, tea, and blackberry.

Multivalent antigen binding proteins according to the invention may be prepared by transforming a host by incorporating a gene encoding the polypeptide as set forth above and expressing said gene in said host.

Suitably the host or hosts may be selected from prokaryotic bacteria, such as Gram-negative bacteria, for example

E. coli,

and Gram-positive bacteria, for example

B. subtilis

or lactic acid bacteria, lower eukaryotes such as yeasts, for example belonging to the genera Saccharomyces, Kluyveromyces, Hansenula or Pichia, or moulds such as those belonging to the genera Aspergillus or Trichoderma.

Preferred hosts for use in connection with the present invention are the lower eukaryotic moulds and yeasts.

Techniques for synthesising genes, incorporating them into hosts and expressing genes in hosts are well known in the art and the skilled person would readily be able to put the invention into effect using common general knowledge.

Methods for producing antibody fragments or functionalised fragments thereof derived from the heavy chain immunoglobulin of Camelidae using a transformed lower eukaryotic host are described, for example in patent application WO 94/25591 and such techniques may suitably be applied to prepare constructs according to the present invention.

Proteins according to the invention may be recovered and purified using conventional techniques such as affinity chromatography, ion exchange chromatography or gel filtration chromatography.

The activity of the multivalent binding proteins according to the invention may conveniently be measured by standard techniques known in the art such as enzyme-linked immunoadsorbant assay (ELISA), radioimmune assay (RIA) or by using biosensors.

The following examples are provided by way of illustration only. Techniques used for the manipulation and analysis of nucleic acid materials were performed as described in Sambrook et al, Molecular Cloning, Cold Spring Harbor Press, New York:, 2nd Ed.(1989) unless otherwise indicated.

HC-V denotes heavy chain variable domain.

Restriction sites are underlined.

EXAMPLES

Example 1

Induction of Humeral Immune Responses in Llama

Male llamas were immunised with a water in oil emulsion (1:9 V/V, antigen in water: Specol (Bokhout et al.) subcutaneously and intramuscularly. Per immunisation site 0.75-1.5 ml water in oil emulsion was inoculated containing 100:g antigen. The antigens used were: hCG (Sigma), azo-dye RR6 (ICI) which was coupled to BSA via its reactive triazine group and

Streptococcus mutans

HG982 cells. Immunisations were performed according to the following time table: The second immunisation was performed three weeks after the first. The third was performed two weeks after the second immunisation. The immune response was followed by antigen specific ELISAs.

The anti-RR-6 response was measured by using Nunc Covalink plates, which where coated with the azo-dye. After incubation with (diluted) serum samples, the bound llama antibodies were detected via a incubation with poly-clonal rabbit-anti-llama antiserum (obtained via immunising rabbits with llama immunoglobulines which were purified via ProtA and ProtG columns; ID-DLO), followed by an incubation with swine-anti-rabbit immunoglobulines (Dako) conjugated with alkaline phosphatase. Finally the alkaline phosphatase enzyme-activity was determined after incubation with p-nitro-phenyl phosphate and the optical density was measured at 405 nm. The anti-hCG response, was measured in essentially the same way using Nunc maxi-sorb plates coated with hCG. The anti-Streptococcus response, was measured in essentially the same way using nunc maxi-sorb plates sensitised with

Streptococcus mutans

HG982.

Example 2

Cloning, Expressing and Screening of Llama EC-V Fragments

2.1 Isolation of Gene Fragments Encoding Llama HC-V Domains.

From an immunised llama a blood sample of about 200 ml was taken and an enriched lymphocyte population was obtained via Ficoll (Pharmacia) discontinuous gradient centrifugation. From these cells, total RNA was isolated by acid guanidium thiocyanate extraction (e.g. via the method described by Chomczynnski and Sacchi, 1987). After first strand cDNA synthesis (e.g. with the Amersham first strand cDNA kit), DNA fragments encoding HC-V fragments and part of the long or short hinge region were amplified by PCR using specific primers:

Pst

I

V

H

-2B

5′-AGGTSMAR

CTGCAG

SAGTCWGG-3′

(see SEQ. ID. NO:2)

S = C and G, M = A and C, R = A and G, W = A and T,

Hin

dIII

Lam-07

5′-AACAGTT

AAGCTT

CCGCTTGCGGCCGCGGAGCTGGGGTCTTCGCTGTG

(see SEQ. ID. NO:3)

GTGCC-3′

(short hinge)

Hin

dIII

Lam-08

3′-AACAGTT

AAGCTT

CCGCTTGCGGCCGCTGGTTCTGGTTTTGGTGTCTT

(see SEQ. ID. NO:4)

GGGTT-3′

(long hinge)

Upon digestion of the PCR fragments with PstI (coinciding with codon 4 and 5 of the HC-V domain, encoding the amino acids L-Q) and BstEII (located at the 3′-end of the HC-V gene fragments, coinciding with the amino acid sequence Q-V-T), the DNA fragments with a length between 300 and 400 bp (encoding the HC-V domain, but lacking the first three and the last three codons) were purified via gel electrophoresis and isolation from the agarose gel.

2.2 Construction of

Saccharomyces cerevisiae

Expression Plasmids Encoding Llama HC-V Domains.

Plasmids pUR4547 and pUR4548 are

Saccharomyces cerevisiae

episomal expression plasmids, derived from pSY1 (Harmsen et al., 1993). From pSY1 the PstI site, located in front of the GAL7 promoter was removed after partial digestion with PstI, incubation with Klenow fragment and subsequent blunt end ligation. After transformation the desired plasmid could be selected on the basis of restriction pattern analysis. Subsequently, the BstEII site in the Leu2 selection marker was removed by replacing the about 410 bp AflII/PflMI fragment with a corresponding fragment in which the BstEII site was removed via a three step PCR mutagenesis, using the primers:

(see SEQ. ID. NO:5)

PCR-A:

Pfl

MI

BOLI 1

5′-GGGAATT

CCAATAGGTGG

TTAGCAATCG

(see SEQ. ID. NO:6)

(

Bst

EII)

BOLI 4

5′-GACCAACGT

GGTCGCC

TGGCAAAACG

(see SEQ. ID. NO:7)

PCR-B:

(

Bst

EII)

BOLI 3

5′-CGTTTTGCCA

GGCGACC

ACGTTGGTC

(see SEQ. ID. NO:8)

AfL

II

BOLI 2

5′-CCCCAAGCTTACATGGT

CTTAA

GTTGCCGT

PCR-A was performed with primers BOLI 1 and BOLI 4 and resulted in an about 130 bp fragment with the PflMI restriction site at the 3′-end and the inactivated BstEII site at the 5′-end. PCR-B was performed with primers BOLI 2 and BOLI 3 and resulted in an about 290 bp fragment with the AflII site at the 5′-end. The third PCR was with the fragments obtained from reaction A and B, together with the primers BOLI 1 and BOLI 2.

Finally, the about 1.8 kb SacI-HindIII fragment was replaced with synthetic fragments, having sequences as presented below, resulting the plasmids pUR4547 and pUR4548, respectively.

(see SEQ. ID. NO:9 and NO:10)

Sac

I/

Hind

III fragment of pUR4547

Sac

I

GAGCTCATCACACAAACAAACAAAACAAAATGATGCTTTTGCAAGCCTTCCCTT

1

---------+---------+---------+---------+---------+----

54

CTCGAGTAGTGTGTTTGTTTGTTTTGTTTTACTACGAAAACGTTCGGAAGGGAA

M M L L Q A F L F

|→ SUC2 ss

Pst

I

TTCCTTTTGGCTGGTTTTGCAGCCAAAATATCTGCGCAGGTGCAGCTGCAGG

55

------+---------+---------+---------+---------+-----

105

AAGGAAAACCGACCAAAACGTCGGTTTTATAGACGCGTCCACGTCGACGTCC

L L A G F A A K I S A Q V Q L Q E

|→

Bst

EII

Hind

III

AGTCATAATGAGGGACCCAGGTCACCGTCTCCTCATAATGACTTAAGCTT

106

----+---------+---------+---------+---------+-----

155

TCAGTATTACTCCCTGGGTCCAGTGGCAGAGGAGTATTACTGAATTCGAA

E S * * G T Q V T V S S * *

HC-V cassette ←|

and

(see SEQ. ID. NO:11 and NO:12)

Sac

I/

Hind

III fragment of pUR4548

Sac

I

GAGCTCATCACACAAACAAACAAAACAAAATGATGCTTTTGCAAGCCTTCCTTT

1

---------+---------+---------+---------+---------+----

54

CTCGAGTAGTGTGTTTGTTTGTTTTGTTTTACTACGAAAACGTTCGGAAGGAAA

M M L L Q A F L F

|→ SUC2 ss

Pst

I

TCCTTTTGGCTGGTTTTGCAGCCAAAATATCTGCGCAGGTGCAGCTGCAGG

55

-----+---------+---------+---------+---------+-----

105

AGGAAAACCGACCAAAACGTCGGTTTTATAGACGCGTCCACGTCGACGTCC

L L A G F A A K I S A Q V Q L Q E

|→

Bst

EII

AGTCATAATGAGGGACCCAGGTCACCGTCTCCTCAGAACAAAAACTCATC

106

----+---------+---------+---------+---------+-----

155

TCAGTATTACTCCCTGGGTCCAGTGGCAGAGGAGTCTTGTTTTTGAGTAG

S * * G T Q V T V S S E Q K L I

HC-V cassette ←|→ myc tail

Hind

III

TCAGAAGAGGATCTGAATTAATGACTTAAGCTT

156

----+---------+---------+--------

188

AGTCTTCTCCTAGACTTAATTACTGAATTCGAA

S E E D L N * *

←|

Both plasmids contain the GAL7 promoter and PGK terminator sequences as well as the invertase (SUC2) signal sequence. In both plasmids the DNA sequence encoding the SUC2 signal sequence is followed by the first 5 codons, (encoding Q-V-Q-L-Q=SEQ. ID. NO: 13) of the HC-V domain (including the BstII site), a stuffer sequence, the last six codons (encoding Q-V-T-V-S-S=SEQ. ID. NO: 14) of the HC-V domain. In pUR4547, this is followed by two stop codons, an AflII and HindIII site. In pUR4548, this sequence is followed by eleven codons encoding the myc-tag, two stop codons, an AflII and HindIII site.

Plasmids pUR4547 and pUR4548 were deposited under the Budapest Treaty at the Centraal Bureau voor Schimmelcultures, Baarn on Aug. 18, 1997 with deposition numbers: CBS 100012 and CBS 100013, respectively. In accordance with Rule 28(4) EPC, or a similar arrangement from a state not being a contracting state of the EPC, it is hereby requested that a sample of such deposit, when requested, will be submitted to an expert only.

Upon digesting pUR4548 with PstI and BstEII, the about 6.4 kb vector fragment was isolated and ligated with the PstI-BstEII fragments of about 350 bp obtained as described above. After transformation of

S. cerevisiae,

via electroporation, transformants were selected from minimal medium agar plates (comprising 0.7% yeast nitrogen base, 2% glucose and 2% agar, supplemented with the essential amino acids and bases).

2.3 Screening for Antigen Specific HC-V Domains.

For the production of llama HC-V fragments with myc-tail, individual transformants were grown overnight in selective minimal medium (comprising 0.7% yeast nitrogen base, 2% glucose, supplemented with the essential amino acids and bases) and subsequently diluted ten times in YPGal medium (comprising 1% yeast extract, 2% bacto pepton and 5% galactose). After 24 and 48 hours of growth, the culture supernatant of the colonies was analysed by ELISA for the presence of HC-V fragments which specifically bind to the antigens hCG, RR6 or Streptococcus in essential the same way as described in Example 1. In this case, however, the presence of specifically bound HC-V fragments was detected by incubation with monoclonal anti-myc antibodies, followed by incubation with poly-clonal rabbit-anti-mouse conjugate with alkaline phosphatase. In this way a number of anti-hCG, anti-Streptococcus and anti-RR6 HC-V fragments have been isolated, among which are:

anti-RR6:

R7

pUR4638

(see

FIG. 2

; SEQ. ID. NO: 15 and NO: 16)

R9

pUR4640

(see

FIG. 3

; SEQ. ID. NO: 17 and NO: 18)

anti-hCG (alpha unit):

H14

pUR4601

(see

FIG. 4

; SEQ. ID. NO: 19 and NO: 20)

HI15

pUR4602

(see

FIG. 5

; SEQ. ID. NO: 21 and NO: 22)

anti-

Streptococcus

:

S36

pUR4603

(see

FIG. 6

; SEQ. ID. NO: 23 and NO: 24)

S120

pUR4642

(see

FIG. 7

; SEQ. ID. NO: 25 and NO: 26)

Example 3

Production of Llama HC-V Biheads by

S. cerevisiae

3.1 Construction of Episomal Expression Plasmids Encoding Anti-hCG/Anti-RR6 bispecific Biheads.

In the anti-hCG HC-V fragments HI4 and HI15 (anti-alpha-subunit), the PstI site was removed and a XhoI site was introduced via PCR, using the primers:

MPG158WB

(see SEQ. ID. NO:27)

Xho

I

5′-GAATTAAGCGGCCGCCCAGGTGAAACTG

CTCGAG

TCWGGGGGA-3′

and

MPG159WB

(see SEQ. ID. NO:28)

Bst

EII

3′-CCCTGGGT

CCAGTGG

CAGAGGAGTGGCAGAGGAGTCTTGTTT-5′

In this way the sequence:

(see SEQ. ID. NO:29 and NO:30)

Pst

I

CAG GTC CAG

CTG CAG

GAG TOT GGG

Q V Q L Q E S G

became

(see SEQ. ID. NO:31 and NO:32)

Xho

I

GAG GTG AAA CTG

CTC GAG

TCW GGG

Q V K L L E S G

Upon digesting the PCR fragments with XhoI and BstEII, the about 330 bp fragments were purified via agarose gel electrophoresis and isolation from the gel. The fragments were cloned into pUR4421 (see Example 1 in WO 94/25591) which was digested with the same enzymes, resulting in pJS2 (H14) and pJS3 (HI15). Subsequently, the about 420 bp EagI-HindIII fragments of pJS2 and pJS3 were isolated and ligated in the about 6.6 kb EagI-HindIII vector fragment of the pSY1 plasmid of which the PstI and BstEII sites were removed as described in Example 2.2. The resulting plasmids pJS7 and pJS8, respectively, were digested with BstEII and HindIII, after which the purified vector fragment was religated in the presence of a synthetic linker having the following sequence:

Bst

EII

Pst

I

Hind

III

← MPG 160 WB (49) →

GGTCACCGTCTCCTCACAGGTGCAGCTGCAGGAGTCACTGTAATGACTTAAGCTT

---------+---------+---------+---------+---------+-----

55

CCAGTGGCAGAGGAGTGTCCACGTCGACGTCCTCAGTGACATTACTGAATTCGAA

<− MPG 161 WB (48) →

V T V S S Q V Q L Q E S L * * L K L

MPG 160 WB (49)

(see SEQ. ID. NO:33)

MPG 161 WB (48)

(see SEQ. ID. NO:34)

resulting in plasmids pJS9 and pJS1O. Finally, these plasmids were digested with PstI and HindIII, after which 35 the purified vector fragments of about 7.0 kb were ligated with the PstI-HindIII fragments of about 350 bp of pUR4638 and pUR4640, encoding the anti-RR6 HC-V fragments R7 and R9, respectively, followed by the myc-ta-1. The resulting

S. cerevisiae

episomal expression plasmids pUR4618, pUR4619, pUR4620 and pUR4621 encode a anti-hCG-anti-RR6 bispecific bihead preceded by the SUC2 signal sequence and followed by the myc-tail.

pUR4618:

SUC2 - H14 - R7 - myc

(see

FIG. 27

; SEQ. ID. NO: 35 and NO: 36)

pUR4619:

SUC2 - H14 - R9 - myc

(see

FIG. 8-9

; SEQ. ID. NO: 37 and NO: 38)

pUR4620:

SUC2 - HI15 - R7 - myc

(see

FIG. 10

; SEQ. ID. NO: 39 and NO: 40)

pUR4621:

SUC2 - HI15 - R9 - myc

(see

FIG. 11

; SEQ. ID. NO: 41 and NO: 42)

Upon digesting these plasmids with XhoI and partially with BstEII, XhoI-BstEII fragments of about 0.7 kb can be isolated and subsequently cloned into the vector fragment of pUR4547 (digested with the same enzymes). In this way biheads can be obtained without the myc tail.

It will be appreciated that expression vectors can be constructed in which different promoter systems, e.g. the constitutive GAPDH promoter or different signal sequences, e.g. the mating factor prepro sequence are used.

3.2 Construction of Episomal Expression Plasmids Encoding Anti-RR6 Bivalent Biheads.

Upon digesting plasmids pUR4618 and pUR4619 with BstEII (partially) and HindIII, DNA fragments of about ˜440 and ˜400 bp could be purified, respectively. These fragments were subsequently ligated with the BstEII-HindIII vector fragment (˜6.7 kb) of pUR4638 resulting in pUR4622 and pUR4623 (see

FIGS. 12-13

; SEQ. ID. NOS: 43/44 and 45/46, respectively), encoding a homodimeric bivalent and a heterodimeric bivalent bihead, respectively.

pUR4622:

SUC2 - R7 - R7 - myc

pUR4623:

SUC2 - R7 - R9 - myc

3.3 Production and Analysis of the HC-V Biheads.

After introducing the expression plasmids pUR4618 through pUR4623 into

S. cerevisiae

via electroporation, transformants were selected from minimal medium agar plates as described in Example 2.3. For the production of biheads, the transformants were grown overnight in selective minimal medium and subsequently diluted ten times in YPGal medium. After 24 and 48 hours of growth, samples were taken for Western blot analysis. For the immuno detection of the produced biheads via Western blot analysis, monoclonal anti-myc antibodies were used, followed by incubation with poly-clonal rabbit-anti-mouse conjugate with alkaline phosphatase.

Bi-Functionality of the Bispecific Biheads was Tested as Follows:

PINs coated with hCG were incubated with (diluted) medium samples. Subsequently, the PINs were incubated with a RR6-alkaline phosphatase conjugate, in which the azo-dye RR6 was coupled to the alkaline phospathase via its reactive triazine group. Finally the alkaline phosphatase enzyme-activity was determined after incubation of the PINs with p-nitro-phenyl phosphate and the optical density was measured at 405 nm (see FIG.

14

).

Bi-Functionality of the Mono-Specific, Bivalent Biheads was Tested as Follows:

Nunc Covalink plates, coated with RR6 were incubated with (diluted) medium samples. Subsequently, they were incubated with a RR6-alkaline phosphatase conjugate, in which the azo-dye RR6 was coupled to the alkaline phospathase via its reactive triazine group. Finally the alkaline phosphatase enzyme-activity was determined after incubation with p-nitro-phenyl phosphate and the optical density was measured at 405 nm (see FIG.

15

).

Example 4

Production of HC-V Biheads by

P. pastoris

4.1 Construction of Integration Vectors for the Expression of Anti-hCG/Anti-RR6 Bispecific Biheads.

To allow the expression and secretion of the Llama bihead constructs in

P. pastoris

, the gene encoding the bispecific construct was fused to the alpha-mating factor leader sequence in the commercially available

P. pastoris

expression vector pPIC9 (Invitrogen). The construction of the final expression vectors involved several cloning steps.

Step 1:

The construction of the bispecific HCV expression vectors required the construction of two shuttle vectors, pPIC9N and pUC.HCVx2. For pUC.HCVx2 the HindIII/EcoRI polylinker of pUC19 was replaced with a synthetic HindIII/EcoRI fragment, destroying the original HindIII site, introducing a NheI site which allows the direct fusion to the alpha-Mating Factor leader sequence in pPIC9N, and introducing the XhoI and HindIII HCVx2 insertion sites.

Synthetic Insert of pUC.HCVx2:

(see SEQ. ID. NO:47 and NO:48)

----A S Q V K L L E-----

AAGCT

GCTAGC

CAGGTGAAACTGCTCGAGCCCGGG

AAGCTT

GAATTC

NheI XhoI

Hind

III

The synthetic linker was constructed by annealing the synthetic oligonucleotides PCR.650 and PCR.651.

PCR.650:

5′-AGCTGCTAGCCAGGTGAAACTGCTCGAGCCCGGGAAGCTTG-3′

(see SEQ. ID. NO: 49)

PCR.651:

5′-AATTCAAGCTTCCCGGGCTCGAGCAGTTTCACCTGGCTAGC-3′

(see SEQ. ID. NO: 50)

The XhoI/HindIII gene fragments encoding the bispecific HCV fragments were excised from pUR4619 and pUR4621 (see Example 3.1) and inserted into the XhoI/HindIII opened pUC.HCVx2 shuttle vector, thus yielding the intermediate constructs pUC.HCV.19 and pUC.HCV21. For pPIC9N the XhoI/EcoRI polylinker of pPIC9 (Invitrogen) was replaced with a synthetic XhoI/EcoRI fragment which introduces a NheI restriction site immediately downstream of the alpha-Mating Factor leader sequence.

(see SEQ. ID. NO:51 and NO:52)

L E K R A S

CTCG

AGAAAAGA

GCTAGC

CCCGGG

GAATTC

XhoI NheI EcoRI

The new insert was constructed by annealing the synthetic oligonucleotides PCR.648 and PCR.649.

PCR.648:

5′-TCGAGAAAAGAGCTAGCCCCGGGG-3′

(see SEQ. ID. NO: 53)

PCR.649:

5′-AATTCCCCGGGGCTAGCTCTTTTC-3′

(see SEQ. ID. NO: 54)

Step 2:

The final expression vectors were constructed via a three point ligation. The BamHI/NheI fragment from pPIC9N which contains the alpha-Mating Factor encoding sequence and the NheI/EcoRI HCVx2 inserts from pUC.HCV21 and pUC.HCV19 were cloned together into a BamHI/EcoRI opened pPIC9 vector. This resulted in the isolation of the

P. pastoris

transformation and expression vectors pPIC.HCV19 and pPIC.HCV21 respectively.

4.2 Production and Analysis of HC-V Biheads.

Step 1: Transformation and Selection of Transformed

P. pastoris

Cells:

P. pastoris

cells were transformed essentially as described by Faber et al. Briefly:

P. pastoris

GS115 cells were grown overnight at 30EC in 500 ml YPD medium (1% Yeast Extract, 2% Peptone, 1% Glucose) too OD

600

=1.4. The cells were spun and the pellet was washed with sterile distilled water before re-suspending in 100 ml KDTT buffer (50 mM Potassium Phosphate pH 7.5, 25 mM DTT). After 15 minutes incubation at 37EC the cells were pelleted (3 minuntes 3000 rpm) and re-suspended in 100 ml ice-cold STM buffer (92.4 g Glucose/l, 10 mM Tris.HCl pH 7.5, 1 mM MgCl

2

). After 5 washes with this buffer the cell pellet was re-suspended in a final volume of 0.5 ml STM buffer. Approximately 2-5 μg DNA in 2 μl H

2

O (BglII digested pPIC constructs: DNA purified via Phenol/Chloroform extractions and precipitation) was mixed with 70 μl of fresh competent

P. pastoris

cells (on ice). The cells were electroporated in a 0.2 cm cuvette at 1.5 kV, 400, 25 μF in a BioRad Gene-Pulser. Immediately after electroporation, 1 ml of YPD medium was added to the cells. After recovery for 1 hour at 30EC, the cells were pelleted and re-suspended in 200 μl M Sorbitol and plated out onto MD plates (1.34% YNB, 4×10

−5

% Biotin, 1% Glucose, 0.15% Agar). Colonies formed by transformed cells (His

+

) were visible within 48 hours incubation at 30EC. Transformed

P. pastoris

cells GS115 were selected essentially as recommended by the Invitrogen

Pichia pastoris

expression manual. The plates containing the His

+

transformants were used to screen for the Mut

+

and Mut

S

phenotype as follows: Using sterile toothpicks, colonies were patched on both an MM plate (1.34% YNB, 4×10

−5

% Biotin, 0.5% MeOH, 0.15% Agar) and an MD plate, in a regular pattern, making sure to patch the MM plate first. Approximately 100 transformants were picked for each construct. After incubating the plates at 30EC for 2-3 days the plates were scored. Colonies that grow normally on the MD plates but show little or no growth on the MM plates were classified as Mut

S

clones.

Step 2: Production and Evaluation of the Bispecific HC-V Biheads.

Transformed and selected

P. pastoris

clones were induced to express bispecific antibody using the protocol outlined below:

1) Using a single colony from the MD plate, inoculate 10 ml of BMGY (1% Yeast Extract, 2% Peptone, 100 mM potassium phosphate pH 6.0, 1.34% YNB, 4×10

−5

% Biotin, 1% Glycerol) in a 50 ml Falcon tube.

2) Grow at 30EC in a shaking incubator (250 rpm) until the culture reaches an OD

600

=2-8.

3) Spin the cultures at 2000 g for 5 minutes and re-suspend the cells in 2 ml of BMMY medium (1% Yeast Extract, 2% Peptone, 100 mM potassium phosphate pH 6.0, 1.34% YNB, 4×10

−5

% Biotin, 0.5% Glycerol).

4) Return the cultures to the incubator.

5) Add 20 μl of MeOH to the cultures after 24 hours to maintain induction.

6) After 48 hours harvest the supernatant by removing the cells by centrifugation.

The crude supernatants were tested for the presence of HC-V bihead fragment via analysis on 12% acrylamide gels using the Bio-Rad mini-Protean II system (FIG.

16

). Bispecific binding activity via shown via ELISA as follows:

1) 96 well ELISA plates (Greiner HC plates) were activated overnight at 37EC with 200 μl/well of the BSA-RR6 conjugate (see Example 1) in PBS.

2) Following one wash with PBST the wells were incubated for 1 hour at 37EC with 200 μl blocking buffer per well. Blocking buffer: 1% BSA in PBS-T.

3) Serial dilutions of test samples (100 μl) were mixed with equal volumes of blocking buffer and added to the sensitised ELISA wells. Incubated at 37EC for 1-2 hours.

4) 200 μl hCG-AP conjugate in blocking buffer was added to each well in which the hCG was coupled to the alkaline phospathase via glutaraldehyde coupling.

5) Following one wash with PBST captured hCG-AP was detected by adding 100 μl/well pNPP substrate (1 mg/ml pNPP in 1M diethanolamine/1 mM MgCl

2

).

Example 5

Production of HC-V Biheads by

H. polymorpha

5.1 Construction of Integration Vectors for the Expression of Anti-hCG/Anti-RR6 Bispecific Biheads.

To allow the expression and secretion of the Llama bihead constructs in

H. polymorpha

strain A16 (Leu-) (Hodgkins et al), the bispecific HC-V gene construct was fused to the alpha-mating factor leader sequence and cloned downstream of the MOX promoter in the

H. polymorpha

transformation and expression vector pHP14.3 (See FIG.

17

). A culture of

E. coli

cells harbouring plasmid pHP14.3 was deposited under the Budapest treaty at the National collection of Type Cultures (Central Public Health Laboratory) in London (United Kingdom) under deposition number NCTC13048. The construction of the final expression vectors involved several cloning steps.

Step 1:

Construction of the pUC19 based shuttle vector pHP.1 in which the HindIII/EcoRI polylinker is replaced with a synthetic HindIII/EcoRI fragment, destroying the original EcoRI site and introducing a BamHI, MunI and two BglII sites:

(see SEQ. ID. NO:55)

AAGCTT

AGATCTGATCCCGGGCAATTGAGATCTAATTC

HindIII Bg1II BamHI MunI BglII

The new insert was constructed by annealing the synthetic oligonucleotides PCR.448 and PCR.449.

PCR.448:

5′-AGCTTAGATCTGGATCCCGGGCAATTGAGATCT-3′

(see SEQ. ID. NO: 56)

PCR.449:

5′-AATTAGATCTCAATTGCCCGGGATCCAGATCTA-3′

(see SEQ. ID. NO: 57)

Step 2:

The alpha-mating factor leader-bispecific HC-V gene from the pPIC9-HCV19 and pPIC9-HCV21 vectors were excised as BamHI-EcoRI fragments and inserted into the BamHI/MunI opened shuttle vector pHP.1 giving pHP1.HCV19 and pHP1.HCV21 respectively.

Step 3:

In the final cloning step, the NheI/BglII inserts from the intermediate constructs pHP1.HCV19 and pHP1.HCV21 were inserted into the NheI/BglII opened

H. polymorpha

transformation vector pHP14.3 yielding pHP14.HCV19 and pHP14.HCV21 respectively.

5.2 Production and Analysis of the HC-V Biheads.

Step 1: Transformation and selection of transformed

H. polymorpha

Cells:

H. polymorpha

cells (strain A16) were transformed essentially as described under 4.2 except that all culturing was done at 37EC and the pHP constructs were digested with SfiI/NotI before transformation. The plates containing the Leu

+

transformants were used to screen for the Mut

+

and Mut

−

0

phenotype as described under 4.2.

Step 2: Production and Evaluation of the Bispecific HC-V Biheads:

Transformed and selected

H. polymorpha

clones were induced to express bispecific antibody using the same protocol used to express HC-V bihead in

P. pastoris

as described under 4.2. The crude supernatants were tested for the presence of HC-V bihead fragment via analysis on 12% acrylamide gels using the Bio-Rad mini-Protean II system (FIG.

18

). Bispecific binding activity via shown via ELISA (see 4.2).

Example 6

Production of Llama HC-V Triple-Heads by

S. cerevisiae

Upon digesting pUR4603 and pUR4642 with BstEII and HindIII, the about 6.8 kb vector fragment can be isolated and religated in the presence of the oligonucleotides MPG160WB and MPG161WB (see Example 3.1). From the resulting plasmids, an about 0.4 kb PstI fragment can be isolated, encoding the anti-Streptococcus HC-V fragments, from which the first five amino acids are lacking at the N-terminus and are fused to the C-terminus. Upon digesting either one of the plasmids pUR4618-pUR4621 with PstI, and subsequently religating the vectors with the about 0.4 PstI fragments obtained as described above, a new set of yeast expression plasmids can be obtained. The orientation of the about 0.4 PstI fragment in the newly obtained plasmid can be determined via a digestion with BstEII. The proper orientation will result in two fragments of about 0.4 kb. The wrong orientation will result in a fragment of about 0.75 and a small fragment of about 0.05 kb. Plasmids with the PstI fragment in the proper orientation will encode tripleheads consisting of an HC-V fragment binding to HCG, directly followed by an HC-V fragment binding to Streptococcus, directly followed by an HC-V fragment binding to RR6 and finally the myc-tail.

It will be appreciated that it is possible (for those skilled in the art) to design alternative construction routes.

Example 7

Reduction of the Infectivity of Lactic Acid Bacteria Phages by the Use of Llama HC-V Biheads

7.1 Coupling of RR6-Dye Molecules to the Phage

To coat the phages with RR6 molecules 10 μl P2 phage stock (˜10

12

phages/ml)+890 μl coupling buffer (0.1M sodium tetraborate, 0.15M NaCl, pH 8.5)+100 μl RR6 solution in coupling buffer, were mixed and incubated for 1 hour at 37EC (ration of 5*10

4

RR6 molecules to 1 phage). To inactivate non-reacted chloro-atoms of RR6, 5 μl blocking buffer (1.0M Tris blocking buffer pH 9, with an excess of primary amino groups) was added and incubated 30 minutes at 37EC.

7.2 Effect of Biheads on the Infectivity of RR6-Coated Phages.

To test the neutralising effect of the anti-RR6 bihead produced by

S. cerevisiae

containing plasmid pUR4623, this bihead was mixed (in a range of 0-300 ng) with 5.5*10

5

phages in 200 μl total volume and incubated for 0.5 hours at 37EC. From this mixture, 100 μl was added to 100 μl of an overnight culture of

Lactococcus lactis

subsp.

cremoris

LM0230, grown in M17 (1*10

9

cfu/ml) and spread on a plate of M17 containing 0.5% glucose and 10 mM CaCl

2

. Plates were incubated overnight at 30EC. In

FIG. 19

it is shown that 14 ng bivalent antibody fragments give a reduction of infection of over 90%.

Example 8

Reduction of the Infectivity of Lactic Acid Bacteria (LAB) Phages by the Use of Llama HC-V Biheads

8.1 Raising Heavy Chain Antibodies against the LAB Phage P2 and Obtaining Antigen Specific HC-V Fragments

An immune response directed against the LAB P2 phages was induced and followed in essentially the same way as described in Example 1. The llama was injected several times with about 0.2 mg phage protein. From the immunised llama an enriched lymphocyte population was obtained and subsequently HC-V gene fragments were obtained as described in Example 2.1. The construction and screening of a yeast HC-V library was performed essentially as described in Examples 2.2 and 2.3.

In this way a number of anti-LAB-phage fragments were obtained. The sequence of three of these are presented below:

pUR3823:

(see SEQ. ID. NO:58)

QVQLQESGGG LVQTGGSLRL SCAASGRTSS DYSVGWFRQA

PGKEREFLAV MMLSGTGTYY ADSVKGRAAI SRDLAKNTVY

LEMNSLKPED TAVYYCALDR AGWLRTEENV YDYWGQGTQV

TVSS

pUR3824:

(see SEQ. ID. NO:59)

QVQLQESGGG LVQPGGSLRL SCAVSGAPFR ESTMAWYRQT

PGKERETVAF ITSGGSKTYG VSVQGRFTIS RDSDRRTVLL

QMNNLQPEDT AVYYCHRALS NTWGQGIQVT VSS

pUR3825:

(see SEQ. ID. NO:60)

QVQLQESGGG LVQPGGSLRL SCVVSGEGFS NYPMGWYRQA

PGKQRELVAA MSEOGDRTNY ADAVKGRFTI SRDNAKKTVY

LQMSSLKPED TAVYYCNAAR WDLGPAPFGS WGQGTQVTVS

S

8.2 Construction of Episomal Expression Plasmids Encoding Anti-LAB-Phage Bivalent Biheads

Episomal expression plasmids encoding bivalent anti-LAB phage biheads were constructed essentially as described in Examples 3.1 and 3.2, using the above mentioned fragments as starting material. In this way amongst others the plasmids pUR3843 and pUR3850 were constructed encoding the bihead preceded by the SUC2 secretion signal.

pUR3843:

SUC2 - 3823 - 3825

pUR3850:

SUC2 - 3825 - 3824

The HC-V biheads 3843 and 3850 were produced by yeast transformants obtained essentially as described in Example 3.3.

8.3 Effect of Biheads on the Infectivity of LAB-Phages

To test the neutralising effect of the anti-LAB-phage biheads produced by

S. cerevisiae

containing plasmids pUR3843 or pUR3850, the biheads were mixed (45 μg of 3843 and 24 μg of 3850) with 10

3

, 10

6

or 10

8

phages in 200 μl total volume. After an incubation for 0.5 hours at 37EC, 100 μl of an overnight culture of

Lactococcus lactis

subsp.

cremoris

LM0230, grown in M17 (1*10

6

cfu/ml) was added to these mixtures. Subsequently the mixture was spread on a plate of M17 containing 0.5% glucose and 10 mM CaCl

2

. Plates were incubated overnight at 30EC after which the number of pfu's was estimated.

TABLE 1

Number of plague forming units

Bihead (μg)

10

3

phages

10

6

phages

10

8

phages

3843 (45)

0

<10

3

Confluent

3850 (24)

0

0

<10

3

8.4 Effect of Biheads on the Acidification of Milk

In a subsequent experiment the acidification of milk upon inoculation with lactic acid bacteria at 30° C. was followed by the simultaneous registration of the pH with a HP-3852A Data Acquisition logger. To this end 100 ml XVM-glucose medium (=skim milk containing 0.35% yeast extract, 0.35% peptone and 1% glucose) was inoculated with 100 μl of an overnight culture of

Lactococcus lactis

subsp.

cremoris

LM0230 in XVM-glucose (10

9

cfu/ml) and incubated for 17 h at 30° C. after addition of 240 μg bihead 3850. The XVM is acidified by the culture in a period of 4 h (

FIG. 25

, graph 1) and is not influenced by the presence of the bihead. When 10

3

pfu/ml P2 phage was added with the LM0230 culture in a parallel experiment, no acidification occurred during the whole period of 17 h (

FIG. 25

, graph 2). When 10

3

, 10

6

, or 10

8

pfu/ml P2 phage was added, together with 240 μg bihead 3850, the acidification by the culture can be completely (in the case of 10

3

cfu/ml phage) or partially restored (

FIG. 25

, graphs 3, 4, 5).

Example 9

Activating Surfaces Using HC-V Biheads Via Self Assembly, for Detection and Purification of Analytes

9.1 Use of Bispecific HC-V Bihead to Form an Active Binding Layer on Polystyrene Wells by Self Assembling onto Pre-Adsorbed Molecules.

In summary, this example shows how double headed antibody fragments can be used to form an active binding layer on polystyrene wells by self assembling onto pre-adsorbed molecules.

FIG. 20

shows a diagrammatic representation of this. The adsorbed antibody surface is shown (A) as is a surface sensitised with double headed antibody fragment (B) made by the self assembly of double headed antibody fragment onto a pre-adsorbed RR6-BSA surface (C). These two surfaces are then able to bind hCG (D).

Preparation of a Reactive Red 6 Bovine Serum Albumin Conjugate

A conjugate of reactive red 6 (RR6) and bovine serum albumin (BSA) was made by incubating 200 μl of RR6 (10 mg/ml in distilled H

2

O) with 1 ml of BSA (10 mg/ml in phosphate buffered saline) with constant mixing for 3 hours at room temperature. A 200 μl solution of ethanolamine (1M in distilled H

2

O) was added and the resulting solution mixed constantly for 15 minutes at room temperature. The BSA-RR6 conjugate was separated from free RR6 by application of 0.75 ml to a PD10 column (Pharmacia) and the column eluted with phosphate buffered saline containing 0.1% sodium azide. The eluent was collected as 1 ml fractions. Fractions 4 and 5 were red in colour and were pooled (the RR6-BSA conjugate elutes before unreacted or free RR6). Fractions 10 onwards were also red in colour but these fractions contain the unbound RR6 and so were discarded.

Preparation of Polystyrene Wells Adsorbed with RR6-BSA

Individual wells from Greiner high binding plates were isolated from a 96 well plate by sawing. Into these wells, 100 μl aliquots of 10 μg/ml of RR6-BSA or monoclonal antibody recognising hCG was added and incubated for 3 hours at room temperature. Both the antibody adsorbed and RR6-BSA adsorbed wells were then washed 3 times with PBSTA.

Self Assembly of a Double Headed Antibody Fragment onto RR6-BSA Wells

Following the PBSTA wash of RR6-BSA wells, 100 μl of affinity purified double headed antibody fragment (HI15-R9: pPIC.HCV2l) at 20 μg/ml in PBSTA was added per well. After 1 hour the RR6-BSA wells were washed 3 times with PBSTA.

Capture of I

125

labelled hCG to Antibody Adsorbed and Double Headed Antibody Fragment Sensitised RR6-BSA Wells

hCG (2500 IU/ml in PBSTA) was spiked with 10 μCi I

125

hCG (Amersham) and then diluted to 500, 100, 20 and 4 IU/ml of hCG with PBSTA. Aliquots (100 μl) of these dilutions were incubated in the wells for 1 hour at room temperature after which time the wells were extensively washed with PBSTA. Wells were then counted on a gamma counter.

FIG. 21

shows the amount of dpm captured by the monoclonal antibody adsorbed wells (A) and by the double headed antibody fragment sensitised wells (B) over a range of hCG concentrations.

The double headed antibody fragment sensitised wells (HI15-R9: pPIC.HCV21) bound approximately twice as much hCG than the adsorbed antibody wells at saturating hCG concentrations. This would indicate that the double headed antibody fragment sensitised wells possessed a higher density of active hCG binding sites than the adsorbed antibody wells.

9.2 Use of Bispecific HC-V Bihead to Self Assemble on Latex Particles for the Detection of Human Chorionic Gonadotrophin (hCG)

Preparation of a RR6-BSA Latex

To 950 μl of 10 mM borate buffer, 0.01% merthiolate, pH 8.5 a 50 μl aliquot of Duke blue latex (10% solids) was added and mixed by inverting. The diluted latex was then centrifuged at 8,000 g for 10 minutes at room temperature, the supernatant removed and the pellet vortexed briefly. The pellet was re-suspended in a solution made up of 900:1 of borate buffer (as above) and 100 μl of the previously prepared RR6-BSA conjugate. Latex particles were sonicated for 10 s using a sonic probe. The solution containing the latex was mixed for 30 minutes at room temperature. Following this the latex was pelleted as before and re-suspended in 1 ml of the borate buffer.

Self Assembly of a Double Headed Antibody Fragment onto RR6-BSA Latex

By virtue of its specificity the double headed antibody fragment: (HI15-R9: pPIC.HCV21) self assembles on the surface of a RR6-BSA latex. This was achieved by incubating 5:1 of the RR6-BSA latex with 3:1 of supernatant from

Pichia pastoris

expressing the bihead HI15-R9 (pPIC.HCV21) made up to 40 μl with phosphate buffered saline containing 0.1% sodium azide and 0.1% Tween 20 (PBSTA) for 15 minutes at room temperature.

Assessing the Self Assembled Double Head for Use in hCG Assay

hCG (10 μl at various concentrations) was added to the self assembled double head RR6-BSA latex and incubated for 15 minutes at room temperature. The mixture was then allowed to flow up a nitrocellulose strip. The nitrocellulose strip had a line of antibody recognising a different epitope to hCG than the double headed antibody fragment (

FIG. 22

shows a schematic representation of the principle). The amount of latex binding at the antibody line was determined by scanning the intensity of the line using an autoreader. The results are shown in FIG.

23

. By way of comparison a latex was made by adsorption of a monoclonal antibody, specific for hCG, using a similar methodology as that for the RR6-BSA latex. This latex was incubated with hCG (10 μl at the various concentrations) and also subjected to the same evaluation on a nitrocellulose strip (results shown in FIG.

23

).

FIG. 23

shows that the self assembling latex compares well with the adsorbed antibody latex. In fact, the hook effect seen with the adsorbed latex (labelled A in

FIG. 23

) at the higher hCG concentrations is less pronounced with the self assembling latex (labelled B in

FIG. 23

) giving the assay a higher range of hCG detection. The most likely explanation for this is an increased number of hCG binding sites on the self assembling latex compared with the adsorbed latex.

9.3 Assembly of Bispecific HC-V Antibody Fragments to a Dextran Surface Coupled with RR6-BSA Conjugate

Preparation of a Bialite Chip Coupled with RR6-BSA

A new CM5 biosensor chip (Biacore AB) was docked into a Bialite biosensor (Biacore AB). The flow rate, of HEPES buffered saline (HBS) was set to 10 μl/min. The RR6-BSA conjugate was amine coupled to the CM5 chip using an amine coupling kit (Biacore AB) according to the manufacturer's instructions. Briefly, two 40 μl injections of NHS/EDC were performed to activate the biosensor chip surface. Following activation, two 40 μl injections of RR6-BSA (diluted 1:10 in 10 mM sodium acetate, pH 4.0) were performed. The biosensor chip surface was then blocked by two injections of 40:1 ethanolamine (1M).

Preparation of a Binding Surface by Self Assembly of Double Headed Antibody Fragment and Subsequent Detection of hCG

Double headed antibody fragment (HI15-R9: pPIC.HCV21) was assembled onto the RR6-BSA coupled dextran surface by injection of 20 μl purified double headed antibody fragment (HI15-R9: pPIC.HCV21, 100 μg/ml in HBS). This can be seen as an increase in response units (RU) on the Bialite sensorgram shown in

FIG. 24

labelled A. hCG was then injected (20 μl of a 10 IU/ml solution made up in HBS). Detection of hCG can be seen by an increase in RU (

FIG. 24

, labelled B).

Example 10

Anti-hCG/Anti-RR6 Bispecific Biheads Containing a Linker Peptide

10.1 Construction of

S. cerevisiae

Episomal Expression Plasmids Encoding Anti-hCG/Anti-RR6 Bispecific Biheads Containing a Linker Peptide.

Between the H14 and the R9 encoding DNA fragments synthetic linkers were introduced encoding different linker peptides. To this end the about 50 bp long BstEII-HindIII fragment of pJS7 (see Example 3.1) was replaced by an about 50 bp long BstEII-HindIII fragment having the following sequence:

MVaJA

(see SEQ. ID. NO:61)

BstE

II

Xba

I

Dra

III

Pst

I

Hind

III

5′

GTCA

CCG

TCTCTAGA

TGGC

CACCAGGTG

CAG

CTGCAG

GAGTCAACTT

A

3′

MVbJA

(see SEQ. ID. NO:62)

3′

G

CAG

AGATCT

ACCG

GTGGTCCAC

GTC

GAGCTC

CTCAGTTGAA

TTCGA

5′

This resulted in pSJ7a. In this plasmid the about 20 bp PstI-HindIII fragment was replaced with the about 370 bp PstI-HindIII fragment encoding the anti-RR6 HC-V fragment R9 and/with the myc-tail of pUR4640 (see Example 3.1) and resulting in pSJ7b.

Upon digesting plasmid pSJ7b with XbaI and DraIII the about 7 kb vector fragment was ligated with five synthetic oligo nucleotide linker fragments presented below:

MV01JA

(see SEQ. ID. NO:63)

5′ CTAGTGGTACTTCCGGTTCCCAG 3′

MV02JA

(see SEQ. ID. NO:64)

3′ ACCATGAAGGCCAAGG 5′

(see SEQ. ID. NO:65)

S

G T S G S

Q

MV03JA

(see SEQ. ID. NO:66)

5′ CTAGTTCTTCATCTGCTTCTGCCTCTTCAGCCCAG 3′

MV04JA

(see SEQ. ID. NO:67)

3′ AAGAAGTAGACGAAGACGGAGAAGTCGG 5′

(see SEQ. ID. NO:68)

S

S S S A S A S S A

Q

MV05JA

(see SEQ. ID. NO:69)

5′ CTAGTGGTTCTCCAGGTTCACCAGGTCAG 3′

MV06JA

(see SEQ. ID. NO:70)

3′ ACCAAGAGGTCCAAGTGGTCCA 5′

(see SEQ. ID. NO:71)

S

G S P G S P G

Q

MV07JA

(see SEQ. ID. NO:72)

5′ CTAGTGCTACTACAACTGGTTCTTCACCAGGTCCAACTCAG 3′

MV08JA

(see SEQ. ID. NO:73)

3′ ACGATGATGTTGACCAAGAAGTGGTCCAGGTTGA 5′

(see SEQ. ID. NO:74)

S

A T T T G S S P G P T

Q

MV09JA

(see SEQ. ID. NO:75)

5′ CTAGTGCTAATCATTCTGGTAATGCTTCTCAG 3′

MV10JA

(see SEQ. ID. NO:76)

3′ ACGATTAGTAAGACCATTACGAAGA 5′

(see SEQ. ID. NO:77)

S

A N H S G N A S

Q

The oligonucleotide linker fragments encode the last amino acid of the N-terminal HC-V fragment (S) and the first amino acid of the C-terminal HC-V fragment, intersected by the connecting linker peptide. This resulted in plasmids pUR5330 to 5334, respectively.

After transformation of

S. cerevisiae

with these plasmids, the production levels of the biheads were determined via Western blot analysis and a anti-hCG ELISA using anti-myc mAb for detection of the bound bihead (see Example 2.3). Production levels are presented in Table 2 below:

TABLE 2

Production

Plasmid

Linker

level (mg/l)

pUR4619

None

11

pUR5330

S-

G-T-S-G-S

-Q

36

pUR5331

S-

S-S-S-A-S-A-S-S-A

-Q

49

pUR5332

S-

G-S-P-G-S-P-G

-Q

33

pUR5333

S-

A-T-T-T-G-S-S-P-G-P-T

-Q

56

pUR5334

S-

A-N-H-S-G-N-A-S

-Q

51

The production levels of the biheads in which the two HC-V domains are separated by a linker peptide (consisting of between 5 and 11 amino acids) were found to be 3 to 5 times higher as found for the bihead in which the two HC-V fragments are connected without a peptide linker.

It is therefore expected that other linker peptides, e.g. the short hinge regions found in the heavy chain antibodies are equally suitable and give even better production yields.

Finally, the bispecificity of the biheads was demonstrated using the ELISA as described in Example 3.3, the results of which are presented in FIG.

26

.

LITERATURE REFERRED TO IN THE EXAMPLES

Chomczynnski, P. and Sacchi, N. (1987) Single step method of RNA isolation by acid guanidium thiocyanate-phenol-chloroform extraction. Analytical Biochem. 162: 156-159.

Bokhout, B. A., Van Gaalen, C., and Van Der Heijden, Ph. J., (1981), A selected water-in-oil emulsion: composition and usefulness as an immunological adjuvant. Vet. Immunol. Immunopath., 2: 491-500

Bokhout, B. A., Bianchi, A. T. J., Van Der Heijden, Ph. J., Scholten, J. W. and Stok, W., (1986), The influence of a water-in-oil emulsion on humoral immunity. Comp. Immun. Microbiol. Infect. Dis., 9: 161-168.

Giuseppin, M. L. F., Lopes, M. T. S., Planta, R. J., Verbakel, J. M. A., Verrips, C. T. (1991) Process for preparing a protein by a yeast transformed by multicopy integration of an expression vector. PCT application WO 91/00920 (UNILEVER)

Harmsen, M. M., Langedijk, A. C., van Tuinen, E., Geerse, R. H., RauP, H. A., Maat, J., (1993) Effect of pmr1 disruption and different signal sequences on the intracellular processing and secretion of

Cyamopsis tetragonoloba

—galactosidase by

S. cerevisiae.

Gene 125 115-123

Faber, K. N., Haima, P., Harder, W., Veenhuis, M and Geert, A. B., (1994) Highly efficient electrotransformation of the yeast Hansenula polymorpha. Current Genetics, 25: 305-310

Hodgkins, M., Mead, D., Ballance, D. J., Goodey, A. and Sudbery, P., (1993) Expression of the Glucose Oxidase Gene from

Aspergillus niger

in

Hansenula Polymorpha

and its use as a reporter gene to isolate regulatory mutations. Yeast, 9:625-635

77

1

11

PRT

Unknown Organism

Description of Unknown Organism Suitable
peptide linking group

1
Glu Gln Lys Leu Ile Ser Glu Glu Asp Leu Asn
1 5 10

2

22

DNA

Artificial Sequence

Description of Artificial Sequence Primer

2
aggtsmarct gcagsagtcw gg 22

3

53

DNA

Artificial Sequence

Description of Artificial Sequence Primer

3
aacagttaag cttccgcttg cggccgcgga gctggggtct tcgctgtggt gcg 53

4

53

DNA

Artificial Sequence

Description of Artificial Sequence Primer

4
aacagttaag cttccgcttg cggccgctgg ttgtggtttt ggtgtcttgg gtt 53

5

28

DNA

Artificial Sequence

Description of Artificial Sequence Primer

5
gggaattcca ataggtggtt agcaatcg 28

6

26

DNA

Artificial Sequence

Description of Artificial Sequence Primer

6
gaccaacgtg gtcgcctggc aaaacg 26

7

26

DNA

Artificial Sequence

Description of Artificial Sequence Primer

7
cgttttgcca ggcgaccacg ttggtc 26

8

30

DNA

Artificial Sequence

Description of Artificial Sequence Primer

8
ccccaagctt acatggtctt aagttggcgt 30

9

155

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

9
gagctcatca cacaaacaaa caaaacaaa atg atg ctt ttg caa gcc ttc ctt 53
Met Met Leu Leu Gln Ala Phe Leu
1 5
ttc ctt ttg gct ggt ttt gca gcc aaa ata tct gcg cag gtg cag ctg 101
Phe Leu Leu Ala Gly Phe Ala Ala Lys Ile Ser Ala Gln Val Gln Leu
10 15 20
cag gag tca taatga ggg acc cag gtc acc gtc tcc tca taatgactta 150
Gln Glu Ser Gly Thr Gln Val Thr Val Ser Ser
25 30 35
agctt 155

10

35

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

10
Met Met Leu Leu Gln Ala Phe Leu Phe Leu Leu Ala Gly Phe Ala Ala
1 5 10 15
Lys Ile Ser Ala Gln Val Gln Leu Gln Glu Ser Gly Thr Gln Val Thr
20 25 30
Val Ser Ser
35

11

188

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

11
gagctcatca cacaaacaaa caaaacaaa atg atg ctt ttg caa gcc ttc ctt 53
Met Met Leu Leu Gln Ala Phe Leu
1 5
ttc ctt ttg gct ggt ttt gca gcc aaa ata tct gcg cag gtg cag ctg 101
Phe Leu Leu Ala Gly Phe Ala Ala Lys Ile Ser Ala Gln Val Gln Leu
10 15 20
cag gag tca taatga ggg acc cag gtc acc gtc tcc tca gaa caa aaa 149
Gln Glu Ser Gly Thr Gln Val Thr Val Ser Ser Glu Gln Lys
25 30 35
ctc atc tca gaa gag gat ctg aat taatgactta agctt 188
Leu Ile Ser Glu Glu Asp Leu Asn
40 45

12

46

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

12
Met Met Leu Leu Gln Ala Phe Leu Phe Leu Leu Ala Gly Phe Ala Ala
1 5 10 15
Lys Ile Ser Ala Gln Val Gln Leu Gln Glu Ser Gly Thr Gln Val Thr
20 25 30
Val Ser Ser Glu Gln Lys Leu Ile Ser Glu Glu Asp Leu Asn
35 40 45

13

5

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
peptide

13
Gln Val Gln Leu Gln
1 5

14

6

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
peptide

14
Gln Val Thr Val Ser Ser
1 5

15

384

DNA

Lama peruana

CDS

(1)..(384)

15
cag gtg cag ctg cag gag tca ggg gga gga ttg gtg cag gct ggg gac 48
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp
1 5 10 15
tct ctg aga ctc tcc tgc gcg gcc tcg gga cgc act tct cat ggg tat 96
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr
20 25 30
ggt ggc tat ggc atg ggc tgg ttc cgc caa att cca ggg aag gag cgt 144
Gly Gly Tyr Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg
35 40 45
gag ctt gtc gca gca att agg tgg agc ggt cgt aat aca tac tat gca 192
Glu Leu Val Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala
50 55 60
gac tcc gtg aag ggc cga ttc acc atc tcc aga gac aac gtc aag gac 240
Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp
65 70 75 80
atg ctg tat ctg caa atg aac agt ttg aaa cct gag gac acg gcc gtt 288
Met Leu Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val
85 90 95
tac act tgt gca gtt cgg acg gtc cgc gtg gtt gac att tcc agt ccg 336
Tyr Thr Cys Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro
100 105 110
gtt ggg ttt gcc tac tgg ggc cag ggg acc cag gtc acc gtc tcc tca 384
Val Gly Phe Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser
115 120 125

16

128

PRT

Lama peruana

16
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr
20 25 30
Gly Gly Tyr Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg
35 40 45
Glu Leu Val Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala
50 55 60
Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp
65 70 75 80
Met Leu Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val
85 90 95
Tyr Thr Cys Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro
100 105 110
Val Gly Phe Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser
115 120 125

17

342

DNA

Lama peruana

CDS

(1)..(342)

17
cag gtg cag ctg cag gag tca ggg gga ggc ttg gtg cag gct ggg gag 48
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Glu
1 5 10 15
tct ctg aaa ctc tcc tgt gca gcc tct gga aac acc ttc agt ggc ggc 96
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser Gly Gly
20 25 30
ttc atg ggc tgg tac cgc cag gct cca ggg aag cag cgc gag ttg gtc 144
Phe Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu Val
35 40 45
gca acc att aat agt aga ggt atc aca aac tat gca gac ttc gtg aag 192
Ala Thr Ile Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe Val Lys
50 55 60
ggc cga ttc acc atc tcc aga gac aat gcc aag aag aca gtg tat ttg 240
Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu
65 70 75 80
gaa atg aac agc ctg gaa cct gaa gac acg gcc gtt tat tac tgt tac 288
Glu Met Asn Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr Cys Tyr
85 90 95
act cac tac ttc aga tcc tac tgg ggt cag ggg acc cag gtc acc gtc 336
Thr His Tyr Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr Val
100 105 110
tcc tca 342
Ser Ser

18

114

PRT

Lama peruana

18
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Glu
1 5 10 15
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser Gly Gly
20 25 30
Phe Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu Val
35 40 45
Ala Thr Ile Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe Val Lys
50 55 60
Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu
65 70 75 80
Glu Met Asn Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr Cys Tyr
85 90 95
Thr His Tyr Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr Val
100 105 110
Ser Ser

19

351

DNA

Lama peruana

CDS

(1)..(351)

19
cag gtg cag ctg cag gag tca ggg gga gga ttg gtg cag gcg ggg ggc 48
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly
1 5 10 15
tct ctg aga ctc tcc tgt gca gcc tct gga cgc acc ggc agt acg tat 96
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Gly Ser Thr Tyr
20 25 30
gac atg ggc tgg ttc cgc cag gct cca ggg aag gag cgt gag tct gta 144
Asp Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ser Val
35 40 45
gca gct att aac tgg gat agt gcg cgc aca tac tat gca agc tcc gtg 192
Ala Ala Ile Asn Trp Asp Ser Ala Arg Thr Tyr Tyr Ala Ser Ser Val
50 55 60
agg ggc cga ttc acc atc tcc aga gac aac gcc aag aag acg gtg tat 240
Arg Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr
65 70 75 80
ctg caa atg aac agc ctg aaa cct gag gac acg gcc gtt tat acc tgt 288
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
85 90 95
ggc gcg ggg gaa ggt ggt act tgg gac tcc tgg ggc cag ggg acc cag 336
Gly Ala Gly Glu Gly Gly Thr Trp Asp Ser Trp Gly Gln Gly Thr Gln
100 105 110
gtc acc gtc tcc tca 351
Val Thr Val Ser Ser
115

20

117

PRT

Lama peruana

20
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Gly Ser Thr Tyr
20 25 30
Asp Met Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ser Val
35 40 45
Ala Ala Ile Asn Trp Asp Ser Ala Arg Thr Tyr Tyr Ala Ser Ser Val
50 55 60
Arg Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
85 90 95
Gly Ala Gly Glu Gly Gly Thr Trp Asp Ser Trp Gly Gln Gly Thr Gln
100 105 110
Val Thr Val Ser Ser
115

21

354

DNA

Lama peruana

CDS

(1)..(354)

21
cag gtg cag ctg cag gag tct ggg gga gaa ttg gtg cag cct ggg ggc 48
Gln Val Gln Leu Gln Glu Ser Gly Gly Glu Leu Val Gln Pro Gly Gly
1 5 10 15
tct ctg aaa ctc tcc tgc gca gcc tct gga ctt acc ttc act aat tat 96
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Leu Thr Phe Thr Asn Tyr
20 25 30
agc atg ggc tgg ttc cgc cag gct cca gga gtg gac cgt gag gcc gta 144
Ser Met Gly Trp Phe Arg Gln Ala Pro Gly Val Asp Arg Glu Ala Val
35 40 45
gcc gct att agc tgg agt ggt gat aac aca tac tat gta agc tcc gtg 192
Ala Ala Ile Ser Trp Ser Gly Asp Asn Thr Tyr Tyr Val Ser Ser Val
50 55 60
aag gga cga ttc acc atc tcc aga gac aac gcc aag aac acg gtg tat 240
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr
65 70 75 80
ctg caa atg aac agc ctg aaa cct caa gac acg gcc gtt tat tac tgt 288
Leu Gln Met Asn Ser Leu Lys Pro Gln Asp Thr Ala Val Tyr Tyr Cys
85 90 95
gca gta aaa ccc gac gat ggt tgg tgg gac tac tgg ggc cag ggg acc 336
Ala Val Lys Pro Asp Asp Gly Trp Trp Asp Tyr Trp Gly Gln Gly Thr
100 105 110
cag gtc acc gtc tcc tca 354
Gln Val Thr Val Ser Ser
115

22

118

PRT

Lama peruana

22
Gln Val Gln Leu Gln Glu Ser Gly Gly Glu Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Leu Thr Phe Thr Asn Tyr
20 25 30
Ser Met Gly Trp Phe Arg Gln Ala Pro Gly Val Asp Arg Glu Ala Val
35 40 45
Ala Ala Ile Ser Trp Ser Gly Asp Asn Thr Tyr Tyr Val Ser Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Lys Pro Gln Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Ala Val Lys Pro Asp Asp Gly Trp Trp Asp Tyr Trp Gly Gln Gly Thr
100 105 110
Gln Val Thr Val Ser Ser
115

23

387

DNA

Lama peruana

CDS

(1)..(387)

23
cag gtg cag ctg cag gag tca ggg gga ggc ttg gtg cag cct ggg ggg 48
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
tct ctg aga ctc tcc tgt gca gcc tct gga ttc gcc ttc aat ctc tac 96
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Ala Phe Asn Leu Tyr
20 25 30
tgg atg tat tgg ttc cgt cag gct cca ggg aag gga ctc gag tgg gtc 144
Trp Met Tyr Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45
tcg agt gct agt cct ggt aat ggt atc act ttc aat aca ttc tac gcg 192
Ser Ser Ala Ser Pro Gly Asn Gly Ile Thr Phe Asn Thr Phe Tyr Ala
50 55 60
gac tcc gtg aag gga cgg ttc gcc atc tcc aga gac aac gcc aaa aac 240
Asp Ser Val Lys Gly Arg Phe Ala Ile Ser Arg Asp Asn Ala Lys Asn
65 70 75 80
aca ctg tat ctg gag atg aac agt cta caa cct gag gac acg gcc gtg 288
Thr Leu Tyr Leu Glu Met Asn Ser Leu Gln Pro Glu Asp Thr Ala Val
85 90 95
tat tat tgt gct gcc gac ccc tcg tat caa ctc gcg gac ttt ttg act 336
Tyr Tyr Cys Ala Ala Asp Pro Ser Tyr Gln Leu Ala Asp Phe Leu Thr
100 105 110
tcg ctg ccg aat gac tac tcg ggc cag gga acc cag gtc acc gtc tcc 384
Ser Leu Pro Asn Asp Tyr Ser Gly Gln Gly Thr Gln Val Thr Val Ser
115 120 125
tca 387
Ser

24

129

PRT

Lama peruana

24
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Phe Ala Phe Asn Leu Tyr
20 25 30
Trp Met Tyr Trp Phe Arg Gln Ala Pro Gly Lys Gly Leu Glu Trp Val
35 40 45
Ser Ser Ala Ser Pro Gly Asn Gly Ile Thr Phe Asn Thr Phe Tyr Ala
50 55 60
Asp Ser Val Lys Gly Arg Phe Ala Ile Ser Arg Asp Asn Ala Lys Asn
65 70 75 80
Thr Leu Tyr Leu Glu Met Asn Ser Leu Gln Pro Glu Asp Thr Ala Val
85 90 95
Tyr Tyr Cys Ala Ala Asp Pro Ser Tyr Gln Leu Ala Asp Phe Leu Thr
100 105 110
Ser Leu Pro Asn Asp Tyr Ser Gly Gln Gly Thr Gln Val Thr Val Ser
115 120 125
Ser

25

369

DNA

Lama peruana

CDS

(1)..(369)

25
cag gtg cag ctg cag gag tca ggg gga gga ctg gtg cag gct ggg gag 48
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Glu
1 5 10 15
agt ctg aga ctc tcc tgt gta gcc tcg ggc ctc tcc ttc agt gaa ttc 96
Ser Leu Arg Leu Ser Cys Val Ala Ser Gly Leu Ser Phe Ser Glu Phe
20 25 30
gtc atg aca tgg ttc cgc cag gct cca ggg aag gag cgt gag ttt gta 144
Val Met Thr Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val
35 40 45
gca gcg att aac tgg atg gat gat cgt aca tat tat gga agt tcc gtg 192
Ala Ala Ile Asn Trp Met Asp Asp Arg Thr Tyr Tyr Gly Ser Ser Val
50 55 60
aag ggc cga ttc ttc atc tcc aaa gac aac gcc aag aac aca gtg tat 240
Lys Gly Arg Phe Phe Ile Ser Lys Asp Asn Ala Lys Asn Thr Val Tyr
65 70 75 80
ctt caa atg aac ggc ctg aaa cct gag gac acg gcc gtt tat tac tgt 288
Leu Gln Met Asn Gly Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
gca gcc agt agg gat tac tat ggc cac aat gcc aat cag tat cgc tac 336
Ala Ala Ser Arg Asp Tyr Tyr Gly His Asn Ala Asn Gln Tyr Arg Tyr
100 105 110
tgg ggc cag ggg acc cag gtc acc gtc tcc tca 369
Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser
115 120

26

123

PRT

Lama peruana

26
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Glu
1 5 10 15
Ser Leu Arg Leu Ser Cys Val Ala Ser Gly Leu Ser Phe Ser Glu Phe
20 25 30
Val Met Thr Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Val
35 40 45
Ala Ala Ile Asn Trp Met Asp Asp Arg Thr Tyr Tyr Gly Ser Ser Val
50 55 60
Lys Gly Arg Phe Phe Ile Ser Lys Asp Asn Ala Lys Asn Thr Val Tyr
65 70 75 80
Leu Gln Met Asn Gly Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Ala Ala Ser Arg Asp Tyr Tyr Gly His Asn Ala Asn Gln Tyr Arg Tyr
100 105 110
Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser
115 120

27

43

DNA

Artificial Sequence

Description of Artificial Sequence Primer

27
gaattaagcg gccgcccagg tgaaactgct cgagtcwggg gga 43

28

42

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

28
tttgttctga ggagacggtg aggagacggt gacctgggtc cc 42

29

24

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

29
cag gtc cag ctg cag gag tct ggg 24
Gln Val Gln Leu Gln Glu Ser Gly
1 5

30

8

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

30
Gln Val Gln Leu Gln Glu Ser Gly
1 5

31

24

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

31
cag gtg aaa ctg ctc gag tcw ggg 24
Gln Val Lys Leu Leu Glu Ser Gly
1 5

32

8

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

32
Gln Val Lys Leu Leu Glu Ser Gly
1 5

33

55

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

33
g gtc acc gtc tcc tca cag gtg cag ctg cag gag tca ctg taatga ctt 49
Val Thr Val Ser Ser Gln Val Gln Leu Gln Glu Ser Leu Leu
1 5 10
aag ctt 55
Lys Leu
15

34

16

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

34
Val Thr Val Ser Ser Gln Val Gln Leu Gln Glu Ser Leu Leu Lys Leu
1 5 10 15

35

714

DNA

Unknown Organism

Description of Unknown Organism Nucleotide
sequence within plasmid pUR4618 which encodes an
anti-hcg anti-RR6 bispecific biheaded antigen
binding protein

35
ctc gag tca ggg gga gga ttg gtg cag gcg ggg ggc tct ctg aga ctc 48
Leu Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly Ser Leu Arg Leu
1 5 10 15
tcc tgt gca gcc tct gga cgc acc ggc agt acg tat gac atg ggc tgg 96
Ser Cys Ala Ala Ser Gly Arg Thr Gly Ser Thr Tyr Asp Met Gly Trp
20 25 30
ttc cgc cag gct cca ggg aag gag cgt gag tct gta gca gct att aac 144
Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ser Val Ala Ala Ile Asn
35 40 45
tgg gat agt gcg cgc aca tac tat gca agc tcc gtg agg ggc cga ttc 192
Trp Asp Ser Ala Arg Thr Tyr Tyr Ala Ser Ser Val Arg Gly Arg Phe
50 55 60
acc atc tcc aga gac aac gcc aag aag acg gtg tat ctg caa atg aac 240
Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu Gln Met Asn
65 70 75 80
agc ctg aaa cct gag gac acg gcc gtt tat acc tgt ggc gcg ggg gaa 288
Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys Gly Ala Gly Glu
85 90 95
ggt ggt act tgg gac tcc tgg ggc cag ggg acc cag gtc acc gtc tcc 336
Gly Gly Thr Trp Asp Ser Trp Gly Gln Gly Thr Gln Val Thr Val Ser
100 105 110
tca cag gtg cag ctg cag gag tca ggg gga gga ttg gtg cag gct ggg 384
Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly
115 120 125
gac tct ctg aga ctc tcc tgc gcg gcc tcg gga cgc act tct cat ggg 432
Asp Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly
130 135 140
tat ggt ggc tat ggc atg ggc tgg ttc cgc caa att cca ggg aag gag 480
Tyr Gly Gly Tyr Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu
145 150 155 160
cgt gag ctt gtc gca gca att agg tgg agc ggt cgt aat aca tac tat 528
Arg Glu Leu Val Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr
165 170 175
gca gac tcc gtg aag ggc cga ttc acc atc tcc aga gac aac gtc aag 576
Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys
180 185 190
gac atg ctg tat ctg caa atg aac agt ttg aaa cct gag gac acg gcc 624
Asp Met Leu Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala
195 200 205
gtt tac act tgt gca gtt cgg acg gtc cgc gtg gtt gac att tcc agt 672
Val Tyr Thr Cys Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser
210 215 220
ccg gtt ggg ttt gcc tac tgg ggc cag ggg acc cag gtc acc 714
Pro Val Gly Phe Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr
225 230 235

36

238

PRT

Unknown Organism

Description of Unknown Organism Bispecific
biheaded antigen binding protein

36
Leu Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly Ser Leu Arg Leu
1 5 10 15
Ser Cys Ala Ala Ser Gly Arg Thr Gly Ser Thr Tyr Asp Met Gly Trp
20 25 30
Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ser Val Ala Ala Ile Asn
35 40 45
Trp Asp Ser Ala Arg Thr Tyr Tyr Ala Ser Ser Val Arg Gly Arg Phe
50 55 60
Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu Gln Met Asn
65 70 75 80
Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys Gly Ala Gly Glu
85 90 95
Gly Gly Thr Trp Asp Ser Trp Gly Gln Gly Thr Gln Val Thr Val Ser
100 105 110
Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly
115 120 125
Asp Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly
130 135 140
Tyr Gly Gly Tyr Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu
145 150 155 160
Arg Glu Leu Val Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr
165 170 175
Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys
180 185 190
Asp Met Leu Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala
195 200 205
Val Tyr Thr Cys Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser
210 215 220
Pro Val Gly Phe Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr
225 230 235

37

672

DNA

Unknown Organism

Description of Unknown Organism Nucleotide
sequence within plasmid pUR4619, which encodes an
anti-hGC-anti-RR6 bispecific biheaded antigen
binding protein

37
ctc gag tca ggg gga gga ttg gtg cag gcg ggg ggc tct ctg aga ctc 48
Leu Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly Ser Leu Arg Leu
1 5 10 15
tcc tgt gca gcc tct gga cgc acc ggc agt acg tat gac atg ggc tgg 96
Ser Cys Ala Ala Ser Gly Arg Thr Gly Ser Thr Tyr Asp Met Gly Trp
20 25 30
ttc cgc cag gct cca ggg aag gag cgt gag tct gta gca gct att aac 144
Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ser Val Ala Ala Ile Asn
35 40 45
tgg gat agt gcg cgc aca tac tat gca agc tcc gtg agg ggc cga ttc 192
Trp Asp Ser Ala Arg Thr Tyr Tyr Ala Ser Ser Val Arg Gly Arg Phe
50 55 60
acc atc tcc aga gac aac gcc aag aag acg gtg tat ctg caa atg aac 240
Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu Gln Met Asn
65 70 75 80
agc ctg aaa cct gag gac acg gcc gtt tat acc tgt ggc gcg ggg gaa 288
Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys Gly Ala Gly Glu
85 90 95
ggt ggt act tgg gac tcc tgg ggc cag ggg acc cag gtc acc gtc tcc 336
Gly Gly Thr Trp Asp Ser Trp Gly Gln Gly Thr Gln Val Thr Val Ser
100 105 110
tca cag gtg cag ctg cag gag tca ggg gga ggc ttg gtg cag gct ggg 384
Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly
115 120 125
gag tct ctg aaa ctc tcc tgt gca gcc tct gga aac acc ttc agt ggc 432
Glu Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser Gly
130 135 140
ggc ttc atg ggc tgg tac cgc cag gct cca ggg aag cag cgc gag ttg 480
Gly Phe Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu
145 150 155 160
gtc gca acc att aat agt aga ggt atc aca aac tat gca gac ttc gtg 528
Val Ala Thr Ile Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe Val
165 170 175
aag ggc cga ttc acc atc tcc aga gac aat gcc aag aag aca gtg tat 576
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr
180 185 190
ttg gaa atg aac agc ctg gaa cct gaa gac acg gcc gtt tat tac tgt 624
Leu Glu Met Asn Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr Cys
195 200 205
tac act cac tac ttc aga tcc tac tgg ggt cag ggg acc cag gtc acc 672
Tyr Thr His Tyr Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr
210 215 220

38

224

PRT

Unknown Organism

Description of Unknown Organism Bispecific
biheaded antigen binding protein

38
Leu Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Gly Ser Leu Arg Leu
1 5 10 15
Ser Cys Ala Ala Ser Gly Arg Thr Gly Ser Thr Tyr Asp Met Gly Trp
20 25 30
Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Ser Val Ala Ala Ile Asn
35 40 45
Trp Asp Ser Ala Arg Thr Tyr Tyr Ala Ser Ser Val Arg Gly Arg Phe
50 55 60
Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu Gln Met Asn
65 70 75 80
Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys Gly Ala Gly Glu
85 90 95
Gly Gly Thr Trp Asp Ser Trp Gly Gln Gly Thr Gln Val Thr Val Ser
100 105 110
Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly
115 120 125
Glu Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser Gly
130 135 140
Gly Phe Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu
145 150 155 160
Val Ala Thr Ile Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe Val
165 170 175
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr
180 185 190
Leu Glu Met Asn Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr Cys
195 200 205
Tyr Thr His Tyr Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr
210 215 220

39

717

DNA

Unknown Organism

Description of Unknown Organism Nucleotide
sequence within plasmid pUR4620, which encodes an
anti-hCG-anti-RR6 bispecific biheaded antigen
binding protein

39
ctc gag tct ggg gga gaa ttg gtg cag cct ggg ggc tct ctg aaa ctc 48
Leu Glu Ser Gly Gly Glu Leu Val Gln Pro Gly Gly Ser Leu Lys Leu
1 5 10 15
tcc tgc gca gcc tct gga ctt acc ttc act aat tat agc atg ggc tgg 96
Ser Cys Ala Ala Ser Gly Leu Thr Phe Thr Asn Tyr Ser Met Gly Trp
20 25 30
ttc cgc cca ggt cca gga gtg gac cgt gag gcc gta gcc gct att agc 144
Phe Arg Pro Gly Pro Gly Val Asp Arg Glu Ala Val Ala Ala Ile Ser
35 40 45
tgg agt ggt gat aac aca tac tat gta agc tcc gtg aag gga cga ttc 192
Trp Ser Gly Asp Asn Thr Tyr Tyr Val Ser Ser Val Lys Gly Arg Phe
50 55 60
acc atc tcc aga gac aac gcc aag aac acg gtg tat ctg caa atg aac 240
Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr Leu Gln Met Asn
65 70 75 80
agc ctg aaa cct caa gac acg gcc gtt tat tac tgt gca gta aaa ccc 288
Ser Leu Lys Pro Gln Asp Thr Ala Val Tyr Tyr Cys Ala Val Lys Pro
85 90 95
gac gat ggt tgg tgg gac tac tgg ggc cag ggg acc cag gtc acc gtc 336
Asp Asp Gly Trp Trp Asp Tyr Trp Gly Gln Gly Thr Gln Val Thr Val
100 105 110
tcc tca cag gtg cag ctg cag gag tca ggg gga gga ttg gtg cag gct 384
Ser Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala
115 120 125
ggg gac tct ctg aga ctc tcc tgc gcg gcc tcg gga cgc act tct cat 432
Gly Asp Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His
130 135 140
ggg tat ggt ggc tat ggc atg ggc tgg ttc cgc caa att cca ggg aag 480
Gly Tyr Gly Gly Tyr Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys
145 150 155 160
gag cgt gag ctt gtc gca gca att agg tgg agc ggt cgt aat aca tac 528
Glu Arg Glu Leu Val Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr
165 170 175
tat gca gac tcc gtg aag ggc cga ttc acc atc tcc aga gac aac gtc 576
Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val
180 185 190
aag gac atg ctg tat ctg caa atg aac agt ttg aaa cct gag gac acg 624
Lys Asp Met Leu Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr
195 200 205
gcc gtt tac act tgt gca gtt cgg acg gtc cgc gtg gtt gac att tcc 672
Ala Val Tyr Thr Cys Ala Val Arg Thr Val Arg Val Val Asp Ile Ser
210 215 220
agt ccg gtt ggg ttt gcc tac tgg ggc cag ggg acc cag gtc acc 717
Ser Pro Val Gly Phe Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr
225 230 235

40

239

PRT

Unknown Organism

Description of Unknown Organism Bispecific
biheaded antigen binding protein

40
Leu Glu Ser Gly Gly Glu Leu Val Gln Pro Gly Gly Ser Leu Lys Leu
1 5 10 15
Ser Cys Ala Ala Ser Gly Leu Thr Phe Thr Asn Tyr Ser Met Gly Trp
20 25 30
Phe Arg Pro Gly Pro Gly Val Asp Arg Glu Ala Val Ala Ala Ile Ser
35 40 45
Trp Ser Gly Asp Asn Thr Tyr Tyr Val Ser Ser Val Lys Gly Arg Phe
50 55 60
Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr Leu Gln Met Asn
65 70 75 80
Ser Leu Lys Pro Gln Asp Thr Ala Val Tyr Tyr Cys Ala Val Lys Pro
85 90 95
Asp Asp Gly Trp Trp Asp Tyr Trp Gly Gln Gly Thr Gln Val Thr Val
100 105 110
Ser Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala
115 120 125
Gly Asp Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His
130 135 140
Gly Tyr Gly Gly Tyr Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys
145 150 155 160
Glu Arg Glu Leu Val Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr
165 170 175
Tyr Ala Asp Ser Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val
180 185 190
Lys Asp Met Leu Tyr Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr
195 200 205
Ala Val Tyr Thr Cys Ala Val Arg Thr Val Arg Val Val Asp Ile Ser
210 215 220
Ser Pro Val Gly Phe Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr
225 230 235

41

675

DNA

Unknown Organism

Description of Unknown Organism Nucleotide
sequence within plasmid pUR4621, which encodes an
anti-hCG-anti-RR6 bispecific biheaded antigen
binding protein

41
ctc gag tct ggg gga gaa ttg gtg cag cct ggg ggc tct ctg aaa ctc 48
Leu Glu Ser Gly Gly Glu Leu Val Gln Pro Gly Gly Ser Leu Lys Leu
1 5 10 15
tcc tgc gca gcc tct gga ctt acc ttc act aat tat agc atg ggc tgg 96
Ser Cys Ala Ala Ser Gly Leu Thr Phe Thr Asn Tyr Ser Met Gly Trp
20 25 30
ttc cgc cca ggt cca gga gtg gac cgt gag gcc gta gcc gct att agc 144
Phe Arg Pro Gly Pro Gly Val Asp Arg Glu Ala Val Ala Ala Ile Ser
35 40 45
tgg agt ggt gat aac aca tac tat gta agc tcc gtg aag gga cga ttc 192
Trp Ser Gly Asp Asn Thr Tyr Tyr Val Ser Ser Val Lys Gly Arg Phe
50 55 60
acc atc tcc aga gac aac gcc aag aac acg gtg tat ctg caa atg aac 240
Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr Leu Gln Met Asn
65 70 75 80
agc ctg aaa cct caa gac acg gcc gtt tat tac tgt gca gta aaa ccc 288
Ser Leu Lys Pro Gln Asp Thr Ala Val Tyr Tyr Cys Ala Val Lys Pro
85 90 95
gac gat ggt tgg tgg gac tac tgg ggc cag ggg acc cag gtc acc gtc 336
Asp Asp Gly Trp Trp Asp Tyr Trp Gly Gln Gly Thr Gln Val Thr Val
100 105 110
tcc tca cag gtg cag ctg cag gag tca ggg gga ggc ttg gtg cag gct 384
Ser Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala
115 120 125
ggg gag tct ctg aaa ctc tcc tgt gca gcc tct gga aac acc ttc agt 432
Gly Glu Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser
130 135 140
ggc ggc ttc atg ggc tgg tac cgc cag gct cca ggg aag cag cgc gag 480
Gly Gly Phe Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu
145 150 155 160
ttg gtc gca acc att aat agt aga ggt atc aca aac tat gca gac ttc 528
Leu Val Ala Thr Ile Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe
165 170 175
gtg aag ggc cga ttc acc atc tcc aga gac aat gcc aag aag aca gtg 576
Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val
180 185 190
tat ttg gaa atg aac agc ctg gaa cct gaa gac acg gcc gtt tat tac 624
Tyr Leu Glu Met Asn Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr
195 200 205
tgt tac act cac tac ttc aga tcc tac tgg ggt cag ggg acc cag gtc 672
Cys Tyr Thr His Tyr Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val
210 215 220
acc 675
Thr
225

42

225

PRT

Unknown Organism

Description of Unknown Organism Bispecific
biheaded antigen binding protein

42
Leu Glu Ser Gly Gly Glu Leu Val Gln Pro Gly Gly Ser Leu Lys Leu
1 5 10 15
Ser Cys Ala Ala Ser Gly Leu Thr Phe Thr Asn Tyr Ser Met Gly Trp
20 25 30
Phe Arg Pro Gly Pro Gly Val Asp Arg Glu Ala Val Ala Ala Ile Ser
35 40 45
Trp Ser Gly Asp Asn Thr Tyr Tyr Val Ser Ser Val Lys Gly Arg Phe
50 55 60
Thr Ile Ser Arg Asp Asn Ala Lys Asn Thr Val Tyr Leu Gln Met Asn
65 70 75 80
Ser Leu Lys Pro Gln Asp Thr Ala Val Tyr Tyr Cys Ala Val Lys Pro
85 90 95
Asp Asp Gly Trp Trp Asp Tyr Trp Gly Gln Gly Thr Gln Val Thr Val
100 105 110
Ser Ser Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala
115 120 125
Gly Glu Ser Leu Lys Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser
130 135 140
Gly Gly Phe Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu
145 150 155 160
Leu Val Ala Thr Ile Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe
165 170 175
Val Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val
180 185 190
Tyr Leu Glu Met Asn Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr
195 200 205
Cys Tyr Thr His Tyr Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val
210 215 220
Thr
225

43

750

DNA

Unknown Organism

Description of Unknown Organism Nucleotide
sequence within plasmid pUR4622, which encodes a
homodimeric bivalent anti-RR6 antigen binding
protein

43
ctg cag gag tca ggg gga gga ttg gtg cag gct ggg gac tct ctg aga 48
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp Ser Leu Arg
1 5 10 15
ctc tcc tgc gcg gcc tcg gga cgc act tct cat ggg tat ggt ggc tat 96
Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr Gly Gly Tyr
20 25 30
ggc atg ggc tgg ttc cgc caa att cca ggg aag gag cgt gag ctt gtc 144
Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg Glu Leu Val
35 40 45
gca gca att agg tgg agc ggt cgt aat aca tac tat gca gac tcc gtg 192
Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala Asp Ser Val
50 55 60
aag ggc cga ttc acc atc tcc aga gac aac gtc aag gac atg ctg tat 240
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp Met Leu Tyr
65 70 75 80
ctg caa atg aac agt ttg aaa cct gag gac acg gcc gtt tac act tgt 288
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
85 90 95
gca gtt cgg acg gtc cgc gtg gtt gac att tcc agt ccg gtt ggg ttt 336
Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro Val Gly Phe
100 105 110
gcc tac tgg ggc cag ggg acc cag gtc acc gtc tcc tca cag gtg cag 384
Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gln Val Gln
115 120 125
ctg cag gag tca ggg gga gga ttg gtg cag gct ggg gac tct ctg aga 432
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp Ser Leu Arg
130 135 140
ctc tcc tgc gcg gcc tcg gga cgc act tct cat ggg tat ggt ggc tat 480
Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr Gly Gly Tyr
145 150 155 160
ggc atg ggc tgg ttc cgc caa att cca ggg aag gag cgt gag ctt gtc 528
Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg Glu Leu Val
165 170 175
gca gca att agg tgg agc ggt cgt aat aca tac tat gca gac tcc gtg 576
Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala Asp Ser Val
180 185 190
aag ggc cga ttc acc atc tcc aga gac aac gtc aag gac atg ctg tat 624
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp Met Leu Tyr
195 200 205
ctg caa atg aac agt ttg aaa cct gag gac acg gcc gtt tac act tgt 672
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
210 215 220
gca gtt cgg acg gtc cgc gtg gtt gac att tcc agt ccg gtt ggg ttt 720
Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro Val Gly Phe
225 230 235 240
gcc tac tgg ggc cag ggg acc cag gtc acc 750
Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr
245 250

44

250

PRT

Unknown Organism

Description of Unknown Organism A homodimeric
bivalent anti-RR6 antigen binding protein

44
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp Ser Leu Arg
1 5 10 15
Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr Gly Gly Tyr
20 25 30
Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg Glu Leu Val
35 40 45
Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp Met Leu Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
85 90 95
Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro Val Gly Phe
100 105 110
Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gln Val Gln
115 120 125
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp Ser Leu Arg
130 135 140
Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr Gly Gly Tyr
145 150 155 160
Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg Glu Leu Val
165 170 175
Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala Asp Ser Val
180 185 190
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp Met Leu Tyr
195 200 205
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
210 215 220
Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro Val Gly Phe
225 230 235 240
Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr
245 250

45

708

DNA

Unknown Organism

Description of Unknown Organism Nucleotide
sequence within plasmid pUR4623, which encodes a
heterodimeric bivalent anti-RR6 antigen binding
protein

45
ctg cag gag tca ggg gga gga ttg gtg cag gct ggg gac tct ctg aga 48
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp Ser Leu Arg
1 5 10 15
ctc tcc tgc gcg gcc tcg gga cgc act tct cat ggg tat ggt ggc tat 96
Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr Gly Gly Tyr
20 25 30
ggc atg ggc tgg ttc cgc caa att cca ggg aag gag cgt gag ctt gtc 144
Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg Glu Leu Val
35 40 45
gca gca att agg tgg agc ggt cgt aat aca tac tat gca gac tcc gtg 192
Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala Asp Ser Val
50 55 60
aag ggc cga ttc acc atc tcc aga gac aac gtc aag gac atg ctg tat 240
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp Met Leu Tyr
65 70 75 80
ctg caa atg aac agt ttg aaa cct gag gac acg gcc gtt tac act tgt 288
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
85 90 95
gca gtt cgg acg gtc cgc gtg gtt gac att tcc agt ccg gtt ggg ttt 336
Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro Val Gly Phe
100 105 110
gcc tac tgg ggc cag ggg acc cag gtc acc gtc tcc tca cag gtg cag 384
Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gln Val Gln
115 120 125
ctg cag gag tca ggg gga ggc ttg gtg cag gct ggg gag tct ctg aaa 432
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Glu Ser Leu Lys
130 135 140
ctc tcc tgt gca gcc tct gga aac acc ttc agt ggc ggc ttc atg ggc 480
Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser Gly Gly Phe Met Gly
145 150 155 160
tgg tac cgc cag gct cca ggg aag cag cgc gag ttg gtc gca acc att 528
Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu Val Ala Thr Ile
165 170 175
aat agt aga ggt atc aca aac tat gca gac ttc gtg aag ggc cga ttc 576
Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe Val Lys Gly Arg Phe
180 185 190
acc atc tcc aga gac aat gcc aag aag aca gtg tat ttg gaa atg aac 624
Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu Glu Met Asn
195 200 205
agc ctg gaa cct gaa gac acg gcc gtt tat tac tgt tac act cac tac 672
Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr Cys Tyr Thr His Tyr
210 215 220
ttc aga tcc tac tgg ggt cag ggg acc cag gtc acc 708
Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr
225 230 235

46

236

PRT

Unknown Organism

Description of Unknown Organism A
heterodimeric bivalent anti-RR6 antigen binding protein

46
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Asp Ser Leu Arg
1 5 10 15
Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser His Gly Tyr Gly Gly Tyr
20 25 30
Gly Met Gly Trp Phe Arg Gln Ile Pro Gly Lys Glu Arg Glu Leu Val
35 40 45
Ala Ala Ile Arg Trp Ser Gly Arg Asn Thr Tyr Tyr Ala Asp Ser Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Val Lys Asp Met Leu Tyr
65 70 75 80
Leu Gln Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Thr Cys
85 90 95
Ala Val Arg Thr Val Arg Val Val Asp Ile Ser Ser Pro Val Gly Phe
100 105 110
Ala Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser Gln Val Gln
115 120 125
Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Ala Gly Glu Ser Leu Lys
130 135 140
Leu Ser Cys Ala Ala Ser Gly Asn Thr Phe Ser Gly Gly Phe Met Gly
145 150 155 160
Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu Val Ala Thr Ile
165 170 175
Asn Ser Arg Gly Ile Thr Asn Tyr Ala Asp Phe Val Lys Gly Arg Phe
180 185 190
Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr Leu Glu Met Asn
195 200 205
Ser Leu Glu Pro Glu Asp Thr Ala Val Tyr Tyr Cys Tyr Thr His Tyr
210 215 220
Phe Arg Ser Tyr Trp Gly Gln Gly Thr Gln Val Thr
225 230 235

47

47

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

47
aagct gct agc cag gtg aaa ctg ctc gag cccgggaagc ttgaattc 47
Ala Ser Gln Val Lys Leu Leu Glu
1 5

48

8

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

48
Ala Ser Gln Val Lys Leu Leu Glu
1 5

49

41

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
oligonucleotide

49
agctgctagc caggtgaaac tgctcgagcc cgggaagctt g 41

50

41

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
oligonucleotide

50
aattcaagct tcccgggctc gagcagtttc acctggctag c 41

51

30

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

51
ctc gag aaa aga gct agc cccggggaat tc 30
Leu Glu Lys Arg Ala Ser
1 5

52

6

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

52
Leu Glu Lys Arg Ala Ser
1 5

53

24

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
oligonucleotide

53
tcgagaaaag agctagcccc gggg 24

54

24

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
oligonucleotide

54
aattccccgg ggctagctct tttc 24

55

39

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
insert

55
aagcttagat ctggatcccg ggcaattgag atctaattc 39

56

33

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
oligonucleotide

56
agcttagatc tggatcccgg gcaattgaga tct 33

57

33

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
oligonucleotide

57
aattagatct caattgcccg ggatccagat cta 33

58

124

PRT

Unknown Organism

Description of Unknown Organism Anti-LAB-phage
fragment

58
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Thr Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Ala Ser Gly Arg Thr Ser Ser Asp Tyr
20 25 30
Ser Val Gly Trp Phe Arg Gln Ala Pro Gly Lys Glu Arg Glu Phe Leu
35 40 45
Ala Val Met Met Leu Ser Gly Thr Gly Thr Tyr Tyr Ala Asp Ser Val
50 55 60
Lys Gly Arg Ala Ala Ile Ser Arg Asp Leu Ala Lys Asn Thr Val Tyr
65 70 75 80
Leu Glu Met Asn Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Ala Leu Asp Arg Ala Gly Trp Leu Arg Thr Glu Glu Asn Val Tyr Asp
100 105 110
Tyr Trp Gly Gln Gly Thr Gln Val Thr Val Ser Ser
115 120

59

113

PRT

Unknown Organism

Description of Unknown Organism Anti-LAB-phage
fragment

59
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Ala Val Ser Gly Ala Pro Phe Arg Glu Ser
20 25 30
Thr Met Ala Trp Tyr Arg Gln Thr Pro Gly Lys Glu Arg Glu Thr Val
35 40 45
Ala Phe Ile Thr Ser Gly Gly Ser Lys Thr Tyr Gly Val Ser Val Gln
50 55 60
Gly Arg Phe Thr Ile Ser Arg Asp Ser Asp Arg Arg Thr Val Leu Leu
65 70 75 80
Gln Met Asn Asn Leu Gln Pro Glu Asp Thr Ala Val Tyr Tyr Cys His
85 90 95
Arg Ala Leu Ser Asn Thr Trp Gly Gln Gly Ile Gln Val Thr Val Ser
100 105 110
Ser

60

121

PRT

Unknown Organism

Description of Unknown Organism Anti-LAB-
phage fragment

60
Gln Val Gln Leu Gln Glu Ser Gly Gly Gly Leu Val Gln Pro Gly Gly
1 5 10 15
Ser Leu Arg Leu Ser Cys Val Val Ser Gly Glu Gly Phe Ser Asn Tyr
20 25 30
Pro Met Gly Trp Tyr Arg Gln Ala Pro Gly Lys Gln Arg Glu Leu Val
35 40 45
Ala Ala Met Ser Glu Gly Gly Asp Arg Thr Asn Tyr Ala Asp Ala Val
50 55 60
Lys Gly Arg Phe Thr Ile Ser Arg Asp Asn Ala Lys Lys Thr Val Tyr
65 70 75 80
Leu Gln Met Ser Ser Leu Lys Pro Glu Asp Thr Ala Val Tyr Tyr Cys
85 90 95
Asn Ala Ala Arg Trp Asp Leu Gly Pro Ala Pro Phe Gly Ser Trp Gly
100 105 110
Gln Gly Thr Gln Val Thr Val Ser Ser
115 120

61

48

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

61
gtcaccgtct ctagatggcc accaggtgca gctgcaggag tcaactta 48

62

47

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

62
agcttaagtt gactcctcga gctgcacctg gtggccatct agagacg 47

63

23

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

63
ctagtggtac ttccggttcc cag 23

64

16

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

64
ggaaccggaa gtacca 16

65

7

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

65
Ser Gly Thr Ser Gly Ser Gln
1 5

66

35

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

66
ctagttcttc atctgcttct gcctcttcag cccag 35

67

28

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

67
ggctgaagag gcagaagcag atgaagaa 28

68

10

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

68
Ser Ser Ser Ser Ala Ser Ala Ser Ser Ala
1 5 10

69

29

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

69
ctagtggttc tccaggttca ccaggtcag 29

70

22

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

70
acctggtgaa cctggagaac ca 22

71

9

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

71
Ser Gly Ser Pro Gly Ser Pro Gly Gln
1 5

72

41

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

72
ctagtgctac tacaactggt tcttcaccag gtccaactca g 41

73

34

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

73
agttggacct ggtgaagaac cagttgtagt agca 34

74

13

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

74
Ser Ala Thr Thr Thr Gly Ser Ser Pro Gly Pro Thr Gln
1 5 10

75

32

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

75
ctagtgctaa tcattctggt aatgcttctc ag 32

76

25

DNA

Artificial Sequence

Description of Artificial Sequence Synthetic
DNA

76
agaagcatta ccagaatgat tagca 25

77

10

PRT

Artificial Sequence

Description of Artificial Sequence Synthetic
amino acid

77
Ser Ala Asn His Ser Gly Asn Ala Ser Gln
1 5 10

Number	Date	Country
0 368 684	May 1990	EP
9311161	Jun 1993	WO
9413806	Jun 1994	WO
WO 9413806	Jun 1994	WO
9425591	Nov 1994	WO
WO 9634103	Oct 1996	WO
9738102	Oct 1997	WO

Multivalent antigen-binding proteins

Information

Patent Number

Date Filed

Date Issued

Inventors

Original Assignees

Examiners

Agents

CPC

US Classifications

Field of Search

US

International Classifications

Abstract

Description

Claims

Priority Claims (1)

CROSS-REFERENCE TO RELATED APPLICATIONS

PCT Information

US Referenced Citations (1)

Foreign Referenced Citations (7)

Non-Patent Literature Citations (4)

Entry
M. Arbabi-Ghahroudi et al.: “Selection and identification of single domain antibody fragments from camel heavy-chain antibodies.” FEBS Letters, vol. 414, Sep. 15, 1997, pp. 521-526 XP002069903 Amsterdam, The Netherlands p. 525, right-hand co;umn, line 35-line 42 abstract.
H. Hoogenboom: “Mix and match: Building manifold binding sites.” Nature Biotechnology, vol. 15, No. 2, Feb. 1997 pp. 125-126, XP002110046 New York, NY, USA, p. 126, right-hand column, line 30-line 39, figure 1.
D. Neri et al: “High-affinity antigen binding by chelating recombinant antibodies (CRAbs)” Journal of Molecular Biology, vol. 246, 1995, pp. 367-373, XP002092191 Oxford, GB abstract figure 2.
C. Ill et al: “Design and construction of a hybrid immunoglobulin domain with properties of both heavy and light chain variable regions. ” Protein Engineering, vol. 10, No. 8, Aug. 1997, pp. 949-957, XP002110047 Oxford, GB abstract p. 956, right-hand column, line 2-line 30.