CA2302647A1 - Expression of gonadotropins in dictyostelium - Google Patents

Abstract

The present invention relates to gonadotropins expressed in Dictyostelium. The gonadotropins are found to be secreted in a biological active form. Expression of gonadotropins in Dictyostelium provides an easy way to select for gonadotropin mutants.

Description

EXPRESSION OF GONADOTROPINS IN DICTYOSTELIUM
The invention relates to gonadotropins or mutants thereof expressed in Dictyostelium, pharmaceutical compositions containing the same, a method for the s preparation of the gonadotropins as well as a method for the selection of gonadotropin mutants with superagonistic or antagonistic properties.
The gonadotropins form a family of structurally related glycoprotein hormones.
Typical members include chorionic gonadotropin (CG), follicle stimulating hormone (FSH), luteinizing hormone (LH) and thyroid stimulating hormone (TSH). FSH, LH
io and TSH are present in most vertebrate species and are synthesized and secreted by the pituitary. CG has so far been found only in primates, including humans, and in horses and is synthesized by placental tissue.
The hormones are heterodimeric proteins of around 30 kD formed by a non-covalent association of a con-unon a-subunit and a hormone specific ~3-subunit.
is Within a species, the a-subunit is essentially identical for each member of the gonadotropin family; it is also highly conserved from species to species. The (3-subunits are different for each member, i.e. CG, FSH, TSH and LH, but show considerable homology in structure. Furthenmore, also the (3 subunits are highly conserved from species to species. In humans, the a subunit consists of 92 amino acid zo residues, whilst the (3 subunit varies in size for each member: 111 residues in hFSH, 121 residues in hLH, 118 residues in hTSH and 145 residues in hCG (Combarnous, Y. (1992), Endocrine Reviews, ~, 670-691, Lustbader, J.W. et al. (1993), Endocrine Reviews, ~, 291-311). The (3 subunit of hCG is substantially larger than the other ~i subunits in that it contains approximately 34 additional amino acids at the C-terminus z s referred to herein as the carboxy terminal peptide (CTP). This CTP bears four serine linked oligosaccharides.
The gonadotropins serve important functions in a variety of bodily functions including metabolism, temperature regulation and the reproductive process. The hypophyseal gonadotropin FSH for example plays a pivotal role in the stimulation of a o follicle development and maturation whereas LH induces ovulation (Sharp, R.M.
(1990), Clin Endocrinol., ~, 787-807; Dorrington and Armstrong (1979), Recent Prog. Horn. Res., ~5, 301-342). Currently, FSH is applied clinically, either alone or in combination with LH, for ovarian stimulation i.e. ovarian hyperstimulation for in WO 99/13081 PCT/EP9$/057I7 vitro fertilisation (IVF) and induction of in vivo ovulation in infertile anovulatory women (Insler, V.(1988), Int. J. Fertility, ~, 85-97, Navot and Rosenwaks (1988), J.
Vitro Fert. Embryo Transfer, ~, 3-13), as well as for male hypogonadism. The human choriogonadotropin (hCG) is involved in the maintenance of pregnancy in the early s stages after conception and has also important therapeutic applications.
The two subunits of the heterodimer display many conserved infra-subunit disulfide bonds: five disulfide bridges in the a-subunit and six disulfide bridges in the ~3-subunit. The corresponding cysteine residues are fully conserved among all io members of the gonadotropin family. The recently obtained X-ray structure of hCG
shows that these disulfide bonds are involved in typical three-dimensional patterns called disulfide knots.
The gonadotropins possess three or four asparagine residues that can be N-glycosylated and have an important impact on its conformation and biological is activity. In addition the C-terminal peptide (CTP) of hCG can be O-glycosylated at four serine positions. The major role of the glycosylated CTP seems to be the prolongation of the circulatory half life of hCG.
The biosynthesis of the glycoprotein hormones is a highly complex process. In ao the last decade it has become clear that folding, assembly and secretion of gonadotropins is assisted by a large set of chaperones and folding enzymes, residing in the Endoplasmic reticulum and the Golgi apparatus. Since both the a- and the (3-subunit contain a so-called cystine-knot, it can be anticipated that protein disulfide isomerase plays a key role in the facilitation of the folding process. In addition, it has 25 been shown that the N-linked oligosaccharide side chains are required for proper folding, disulfide formation and secretion of hCG (Feng, W. et al (1995) J.
Biol.
Chem. ~Q, 11851-11859). The successful assembly of the two subunits into the dimer is an absolute prerequisite for the biological activity of the dimer.
a o Elucidation of functional determinants of the heterodimeric glycoprotein hormones is often hampered by unwanted secondary effects of mutations on the assembly of the subunits. To facilitate structure/function analyses studies mutants have been produced in which the coding regions of the hCG (3-subunit and the common a-subunit are connected via peptide spacers or intersubunit disulfide bonds. It has been shown that these covalently linked a- and (3-subunits of hCG are able to fold into biologically active conformations.
The gonadotropins have been expressed in Chinese Hamster Ovary (CHO) cells, s and their recombinant derivatives have biological activities comparable to the native hormones (Olijve, W. et al. (1996) Mol. Hum. Reprod. ~, 371-382). This indicates that these host cells contain all chaperones and folding enzymes necessary to assemble the a- and ~3-subunits of hCG and to perform all post-translational modifications necessary for full biological activity. Furthermore, the use of CHO cells io in combination with site-directed mutagenesis has proven to be a valuable tool for elucidating functional determinants in the glycoprotein hormones (Puett, D. et al H.
(1994) in Glycoprotein Hormones (Lustbader, J.W., Puett, D. & Ruddon, R.W., Eds.) pp. 59-82, Springer-Verlag, New-York) and for designing potential new therapeutic analogs of these hormones ( Fares, F.A. et al. ( 1992), Proc Natl Acad Sci U S
A ,$~, is 4304-4308).
Unfortunately, the use of mammalian cells such as CHO cells for the expression of human gonadotropins suffers from some limitations. Thus; it is not possible to generate the high number of transformants necessary for studies that involve random mutagenesis zo of protein domains. Random mutagenesis of selected domains in proteins has been shown to be a valuable tool for identifying the structural determinants for receptor binding and bioactivity. In addition, the use of CHO cells is expensive and labour intensive. Thus, there is a need for the expression of gonadotropins in a more robust expression host.
zs Host cells derived from lower organisms might meet the above mentioned requirements, but it is expected that the complex folding of the gonadotropins hampers proper expression and secretion of such complex recombinant proteins.
Now, unexpectedly it has been found that Dictyostelium is capable of producing the highly complex glycoprotein hormones.
The soil amoebae Dictyostelium discoideum is an organism that provides an attractive alternative for heterologous expression of the human glycoprotein hormones. While it can be grown and transformed with the same ease as the yeast Saccharornyces, it has some of the complex features that resemble mammalian cells, such as glycosylation and chemotaxis. Furthermore, it has recently been shown that Dictyostelium provides a useful system for random mutagenesis approaches.
s Nevertheless, there have been found differences between the glycosylation of proteins produced in Dictyostelium compared to material produced in CHO cells.
It is known that glycosylation plays an important role in hormone function, and whereas most glycosylation is performed by Dictyostelium, galactose, N-acetylgalactosamine or sialic acids are not attached to the oligosaccharide side chains {Slade, M. et al. (1997) io Biotech. Genet. Eng. Rev., fig, 1-35). Though the post-translational modification is not identical to that in higher eukaryotes, gonadotropins produced in Dictyostelium also were found to be biologically active. The protein is found to be capable of binding to its receptor and to stimulate cAMP production in cells expressing the human LH/CG receptor.
15 The heterogeneity of the expressed glycoproteins is greatly reduced leading to much more homogeneous preparations of isohormones. Therefore, gonadotropins produced in Dictyosteliun: are chemically well-defined relative to the more complex CHO-produced gonadotropins. This is a major advantage for the maintenance and analytical validation of the batch-to-batch consistency. Since the glycosylation is a ao very important determinant for the in vivo half live of gonadotropins, production of gonadotropins in Dictyostelium provides a tool to produce non-mutated gonadotropins with well-defined in vivo half lives. In addition, combination of the expression in Dictyostelium with protein engineering facilitates tailor made gonadotropins for several clinical applications.
is Because of the complex inter and intra molecular folding of the two subunits, the large number of disulfide bridges, disulfide knots and post-translational modifications, it is remarkable that active gonadotropins can be expressed in Dictyostelium and that properly folded molecules can be prepared according to the invention. Proper disulfide bond formation is a critical event in the folding and ao maturation of functional gonadotropins. Especially the disulfide bond formation in the (3 subunit is critical: all disulfide bonds are required for efficient combination and folding. Detailed studies of the folding of hCG revealed that the folding of the molecule does not proceed by a simple sequential pathway, but proceeds independently in different domains of the molecule. It was therefore thought that cells of lower organisms were not capable of secreting properly folded gonadotropins.
The present invention provides for gonadotropins expressed in Dictyostelium.
Use of Dictyostelium discoideaun has the advantage that is a well-studied s organism. The vegatative amoebae are easy and inexpensive to grow either in axenic culture or on Gram-negative bacteria. Furthermore, several transformation vectors have been described which are capable of directing expression of foreign proteins.
The gonadotropins according to the invention can be dimeric i.e. composed of two non-covalently bound subunits. Preferably, the gonadotropin is hCG or FSH.
The io gonadotropins, however, can comprise modifications generally known in the art.
In one such preferred modification of the gonadotropins according to the invention, the C-terminus of the amino acid sequence of one of the subunits is linked, optionally through a linker moiety, to the N-terminus of the amino acid sequence of the other subunit. Preferably the linker moiety is a complete or partial CTP
unit or is variant thereof, or a repeated oligopeptide e.g. a 5 times repeated Ser-Gly peptide.
Another modification of the gonadotropins according to the invention can be an extension of the a andlor ~3 subunit at their respective N- or C-terminus with a complete or partial CTP unit or a variant thereof. The extension may comprise the respective CTP units in single or multiple forms. Alternatively, a complete CTP unit ao or partial CTP unit or multiple forms thereof can be inserted in the N- or C-terminus of said subunits. Again another modification is the introduction of one or more non-native disulfide bridges.
Furthermore, the gonadotropins according to the invention may be either glycosylated or partially glycosylated. Partially glycosylated gonadotropins according 25 to the invention can be obtained by site-directed mufagenesis whereby one or more of the glycosyiation recognition sites in the gonadotropins are removed.
Alternatively, the glycosylation pattern of the gonadotropins according to the invention can be modified by the introduction of additional glycosylation recognition sites and, optionally, the removal of one or more glycosylation recognition sites, resulting in a 3o modified glycosylation of said gonadotropins. A glycosylation recognition site as used herein consists of the amino acid sequence Asn-X-SerfThr, wherein X can be any amino acid.

As used herein, the a and (3 subunits of CG, FSH, LH and TSH as well as the heterodimeric fOnllS have in general their conventional definitions and refer to the proteins having the amino acid sequences known in the art per se, or allelic variants thereof, regardless of the glycosylation pattern displayed.
s "Native" forms of these proteins are those proteins which have the amino acid sequences as isolated from the relevant vertebrate tissue, and have these known sequences per se, or their allelic variants thereof.
These "variants" are those proteins which have deliberate alterations in amino acid sequences relative to the native proteins. The alterations may include single or io multiple deletions, insertions, substitutions and combinations thereof, and can be produced by, for example, site specific mutagenesis.
As used herein, the "CTP unit" refers to the amino acid sequence found at the carboxy terminus of the ~3 subunit of hCG which extends from amino acid 112-118 to residue 145 at the C-terminus or to a portion thereof. A "complete" CTP unit contains i5 28-34 amino acids, depending on the N-terminus of the CTP. A "partial" CTP
unit is an amino acid sequence which occurs between positions 112-118 to 145 inclusive, but which has at least one amino acid deleted from the shortest possible complete CTP
unit (amino acid 118-145). "Multiple" CTP units are understood to encompass tandem arrays of the complete CTP unit or partial CTP unit or combinations of both.
zo Methods to constnict the gonadotropin genes according to the invention are well known in the art (Sambrook et al., Molecular Cloning: a Laboratory Manual, Cold Spring Harbor Laboratory Press, Cold Spring Harbor, latest edition).
Techniques for site directed mutagenesis, ligation of additional sequences, PCR, and construction of suitable expression systems are all, by now, well known in the art. Portions or all of 25 the DNA encoding the desired protein can be constructed synthetically using standard solid phase techniques, preferably to include restriction sites for ease of ligation.
Suitable control elements for transcription and translation of the included coding sequence can be provided to the DNA coding sequences.
The invention also provides for a method for the expression of gonadotropins or 3o mutants thereof in Dictyostelium. Said method according to the invention comprises the steps of - transforming a strain of Dictyostelium with a recombinant plasmid vector comprising a DNA sequence encoding the gonadotropin genes or mutated genes under control of Dictyostelium regulatory sequences - culturing the recombinant strain under conditions to allow expression of the DNA sequence and - isolating the expressed protein.
s Preferably the protein to be expressed is a single-chain protein, i.e. the subunits are covalently connected through a spacer molecule. More preferably the gonadotropin is single-chain hCG.
Another aspect of the invention is to provide a method to easily screen for mutated gonadotropins. Said method comprises io - random mutagenesis of gonadotropin genes - insertion of the mutated genes in a Dictyostelium plasmid vector - transforming a strain of Dictyostelium with said recombinant plasmid vector - culturing clones under conditions to allow expression of the DNA sequence - determining the receptor binding / signal transduction ratio and is - isolating clones with a ratio deviating from the ratio determined for wild type gonadotropins.
Preferably, the mutated gonadotropins show a receptor binding which equals the binding of the native protein to its receptor. More preferably, the affinity of the mutated protein to its receptor is higher than its native counterpart. The signal ao transduction has to be at least two-fold higher or lower as compared to the native protein. Preferably, the difference in signal transduction amounts a factor 10.
Proteins exhibiting a high ratio are useful as antagonists whereas proteins with a low ratio can be used as super agonists.
Methods to determine receptor binding as well as in vitro and in vivo assays to zs determine biological activity of gonadotropins are well known.
Random mutagenesis need not to be performed on the complete gonadotropin gene but instead can also be carried out on a single subunit gene or a well-defined region such as e.g. the determinant loop.
In order to introduce random point mutations in the gonadotropin gene(s), 3o amplification of the regions) of interest with Taq DNA polymerise can be employed.
Since Taq DNA polymerise lacks a 3'~5' exonucleolytic editing activity, this enzyme is an error-prone DNA polymerise, with a measured error rate of 10-5 to 10'~
error per nucleotide synthesized. Therefore, use of PCR with Taq DNA
polymerise _g_ under essentially standard reaction conditions can be used to introduce mutations (Zhou, Y. et al. ( 1991 ), Nucl. Acids Res. ~, S2). However, the frequency of mutations using these conditions is adequate for mutagenizing relatively large sequences, but not for small DNA fragments (< 500 bp). The infidelity of Taq DNA
s polymerase can be increased by addition of Mn2+ and the use of relatively high concentrations of dNTP and Mg'-+ (Leungh, D.W. et al. (1989), Technique ~, 1-1S).
An alternative method for the adjustment of the mutation frequency, which also offers the opportunity of influencing the types of mutation, is the use of dITP in combination with limiting amounts of one of the four dNTPs (Spee, J.H. et al.
( 1993), io Nucl. Acids Res. ?~, 777-778). For mutagenesis of short target DNA(< SO
bp), the use of degenerate oligonucleotides seems to be the method of choice (Kirchhoff, F.
and Desrosiers, R.C. (1996), Meth. Molec. Biol. ~, 323-333). Usually, the procedures have four steps. In step one, the region of interest is amplif ed by (modified) PCR. In step two, the amplified DNA is digested with a pair of restriction endonucleases that is cut at each end of the DNA sequence of interest. In step three, the DNA
fragment containing the DNA sequence of interest is ligated with restriction endonuclease digested vector DNA. In step four, the resulting recombinant DNA molecules are introduced into the cells by transfonnation or electroporation.
ao DNA vectors encoding any of the gonadotropins according to the invention are also within the scope of the invention. DNA vectors according to the invention can be obtained by operatively linking the DNA encoding the native gonadotropins or variants thereof to DNA comprising Dictyostelium regulatory sequences.
Optionally, these vectors also might contain regions which contain origins of replication and/or as polypeptide-encoding sequences facilitating extrachromosomal replication.
Such vectors have the advantage that they can replicate extrachromosomally in the Dictyostelium host cell.
As explained, the variant gonadotropins according to the invention can be 3 o agonists or antagonists, depending on the mutation site. The mutation site may lead to subtle changes in the conformation of the molecule. If the mutation site e.g.
is selected in parts of the protein that are associated with receptor binding and/or signal transduction, the excreted protein according to the invention may lead to a partial or complete loss of signal transduction activity. Such altered gonadotropins, wherein the receptor binding properties are retained, can be used as antagonists. Also gonadotropins with improved binding and signal transduction activities may be selected.
The agonist gonadotropins according to the invention can be used for the same s clinical purposes as the native gonadotropins. In addition the proteins can be used as diagnostic tools to detect the presence or absence of antibodies with respect to the native proteins in biological samples. They are also useful as control reagents in assay kits for assessing the levels of gonadotropin hormones in various samples.
Antagonists can be used e.g. in the treatment of gonadotropin dependent tumors;
i o LH/hCG antagonists to prevent LH surges during controlled ovarian hyperstimulation and FSH antagonists for male contraception.
Suitable pharmaceutical compositions according to the invention comprise one or more of the gonadotropins according to the invention and a pharmaceutical acceptable carrier.
is Pharmaceutical acceptable carriers are well known to those skilled in the art and include, for example, sterile satin, lactose, sucrose, calcium phosphate, gelatin, dextrin, agar, pectin, peanut oil, olive oil, sesame oil and water.
Furthermore the pharmaceutical composition according to the invention may comprise one or more stabilizers such as, for example, carbohydrates including 2o sorbitol, mannitol, starch, sucrosedextrin and glucose, proteins such as albumin -or casein, and buffers like alkaline phosphates.
Suitable administration routes are intramuscular injections, subcutaneous injections, intravenous injections or intraperitoneal injections, oral and intranasal administration.
The following examples are illustrative for the invention and should in no way be interpreted as limiting the scope of the invention.

LEGENDS TO THE FIGURES
Figure 1: Plasmids and cloning strategy. (lA) Maps of plasmids MBl2n and MBl2n/PsA. Both plasmids consists of four main fragments, containing E.coli s maintenance sequences (bluescript), blasticidine resistance gene under Dd promoter control (BSR), a cloning cassette with Dd promoter (actl5) and terminator (2H3), and sequences for extrachromosomal maintenance in Dictyostelium (G4/D5, GS/D6).
MBl2n/PsA contains a PsA linker sequence (Table 1) inserted into the unique BgIII
site of MBl2n. (1B) Cloning diagram of JV158. The oligonucleotides used are shown io by the horizontal arrows. The xxx shown in oligonucleotide b20aarev indicate that sequence substitutions have been made to optimize the sequence for Dictyostelium codon preference. ( 1 C) Cloning diagram of JV l OPSA. All oligonucleotide sequences are given in Table 1.
is Figure 2: Binding activity of wildtype hLH, hCG and single chain hCG (sc hCG) produced in Chinese Hamster Ovary cells (CHO) or Dictyostelium discoideun: (Dd) to membranes of CHO cells stably expressing the human LHICG receptor. The membranes were incubated with '25I-labeled hCG in the absence or presence of varying concentrations unlabeled wildtype hLH, hCG or the ao single chain hCG's. Displacement curves are presented as the percentage of maximal binding at each dose of unlabeled hormone.
Figure 3:In vitro biological activity of wildtype hLH, hCG and single chain hCG (sc hCG) produced in Chinese Hamster Ovary cells (CHO) or Dictyostelium 25 discoideurn (Dd). Extracellular cAMP was measured by specific ltIA after stimulation of CHO cells stably expressing the human LH/CG receptor.
Figure 4: Ire vitro biological activity of wildtype hCG produced in Chinese Hamster Ovary cells (CHO) or Dictyostelium discoideum (Dd). Luciferase ao production was measured after 4 h incubation at 37 °C and stimulation of CHO cells stably expressing the human LH/CG receptor and a reporter construct.

Figure 5: In vitro biological activity of wildtype FSH produced in Chinese Hamster Ovary cells (CHO) or Dictyosteliunt discoideum (Dd). Luciferase production was measured after 4 h incubation at 37 °C and stimulation of CHO cells stably expressing the human FSH receptor and a reporter construct.
Figure 6: Li vitro biological activity of wildtype hCG from CHO cells and selected hCG mutants produced by Dictyostelium discoideum (Dd). Luciferase production was measured after 4 h incubation at 37 °C and stimulation of CHO cells stably expressing the human LH/CG receptor and a reporter construct.
io EXAMPLES
is Design of the expression constructs A gonadotropin mutant consisting of a completely intact a-subunit connected via a peptide decamer containing five Ser-Gly repeats to the (3-chain only lacking its C-terminal peptide, was selected for expression in Dictyostelium.
Two constructs were generated, which differ in their leader sequences. The ao first one contains the natural leader sequence of the (3-subunit of hCG. To limit possible problems in mRNA translation due to the presence of a considerable amount (about 40% in the (3-subunit of hCG) of infrequently used codons, the first 30 bases of the coding sequence were altered conform to Dictyostelium preferred codon usage.
For the construction of the second construct it was considered that the proteins as involved in the secretion route of mammalian cells, via the ER and Golgi, may not be conserved between different species. To facilitate transport in Dictyostelium, the leader peptide of the human ~i-subunit was exchanged with a leader peptide of a Dictyostelium glycoprotein, Prespore protein A (PsA), which is transported over the plasma membrane. This leader had been used previously to express secreted ao heterologous proteins (Dittrich ,W. et al. (1994) Bio/Technology ~, 614-618).

The expression plasmids were called JV 158 (adapted codons with (3-subunit leader peptide) and JV10PSA (with the PsA leader peptide) and were derived from MB 12n.
MB 12n is an 8.25 kb extra-chromosomally maintained Dictyostelium discoideum s (Dd) plasmid, containing an unique restriction site between a Dd promoter and terminator. MB 12n consists of 2.9 kb (a CIaI -HincII partial digest fragment) from p155d1 (Hughes, J.E. et al. (1994) Mol. Cell. Biol. ],~, 6117-6124) containing the Dd origin of replication and two Dd genes required for replication (G41D5 and GS/D6), 2.95 kb from pBluescript (Strategene) for propagation in E. coli, 1.35 kb containing is the blasticidine resistance gene between the Dd Actine 15 promoter and the Dd Actin 8 terminator (from pBsr2, Sutoh, K. (1993), Plasmid ~Q, 150-154), and a 1.05 kb cloning cassette containing the Dd Actin 15 promoter, an unique BgIII
restriction site and the Dd 2H3 terminator (from BS 18.2H3, Kumagai A. et al (1989) Cell ~, 265-275). The BgIII site in the blasticidine resistance gene has been removed by is mutagenesis. Figure lA illustrates the relative position of these components in MB 12n. Plasmid MB 12n/PsA contains a linker sequence encoding the 19 amino acid PsA leader peptide (Early, E.A. et al (1988) Mol. Cell. Biol. $ 3458-3466;
Dittrich , et al (1994) Bio/Technology ~, 614-618).cloned in the unique BgIII site. The plasmid has an unique NdeI site in the 3' part of the PsA sequence and an unique BgIII
site 5' ao of the 2H3 terminator, to facilitate 'in frame' directional cloning. The BgIII site adjacent to the Dd Actinl5 promoter was eliminated during cloning (see Table 1).
Using primers b20aarev and alphater (Table 1) a single chain hCG was amplified by PCR from a plasmid containing hCG mutant 1 [(3-(1-111)-(Ser-Gly)5-a-(1-92), (Heikoop, J. C. et al. (1997) Eur. J. Biochem. ~S4 , 656-662). The resulting 25 fragment was cloned in MBl2n after digestion with BgIII. Primer b20aarev is designed to optimize the first 10 amino acids of the (3 chain for codon usage in Dictyostelium. The same template was amplified with primers bmature (Table 1) and alphater to produce a product that, after digestion with NdeI and BgIII, was cloned into MB 12n/PsA. The resulting plasmids were labeled JSV 158 and JV l OPSA, 3 o respectively (see Figure 1 B and 1 C). PCR was performed with the Expand High Fidelity (Boehringer Mannheim) system, using the following cycle parameters:
denaturation for 3 minutes at 94 °C, then 25 cycles with 30 seconds at 94 °C, 30 seconds at 37 °C and 60 seconds at 72 °C. PCR products were separated by gel electrophoresis, excised and purified with Qiaex II (Qiagen) before restriction digestion and cloning. All DNA sequences were analyzed and confirmed by dideoxy sequencing.
Table 1: DNA sequences for oligonucleotides and PsA linker. The PsA sequence s also shows the peptide sequence of the PsA leader, as well as the unique restriction sites BgIII and NdeI.
Oligo ID: Sequence:
io PsA: (BgIII) NdeI BglII
agatcatgaa attccaacat acatttattg cattattatc actattaaca~caaatg c_agatct M K F Q H T F I A L L S L L T Y A N A
b20aarev: gcagatctat ggagatgttc caaggtctcc tccttttatt actcctcagc atgggtggta catgggcatc caag is alphater: ccagatctaa acatttaaga tttgtg bmature: gctatcgaca tatgcaaatg catccaagga gccgcttcg 20 Ex~g~:
Expression of single chain hCG in Dictyostelium Dictyostelium strain AX3 was grown to a density of 2x106 cells per ml in axenic medium before electroporation. The electroporation conditions were basically as described (Mann S.K.O. et al (1994) in: Cell Biology: a Laboratory Handbook, J.E.
25 Celis edt, Academic Press, Vol 1, pp 412-452), using 1 p,g plasmid DNA for electroporation of 10' cells.
Plasmids JV158 and JV10PSA were transformed to Dictyostelium, as well as a MB 12n control plasmid. After electroporation, the cells from one cuvette were seeded in a 10 cm plate. 12 hours after electroporation blasticidine was added to a final concentration of 5 pg/ml. 24 hours after electroporation the medium, containing dead cells, was aspirated, the cells were resuspended by pipetting in medium with blasticidine, and the cells were distributed over 24 wells in a 96 well microtiter plate.
The 24 wells were each serially diluted 10, 100 and 1000 fold. The medium s containing blasticidine was replaced every 3 days. Positive wells were identified 5-9 days after seeding, and transformation efficiency was estimated from the dilution series. Typically, between 1 x 104 and 6 x 104 colonies per pg DNA were obtained.
Single wells were then selected for further experiments. A single well contains 200 p,l of medium, sufficient for a DELFIA~ hLH assay which has a 100% cross-reactivity io with hCG. The assay is based on the direct sandwich technique, in which monoclonal antibodies directed against a specific antigenic site on the ~3-subunit are immobilized.
After binding of intact (single chain) hCG to the solid phase antibody, europium labelled antibodies directed against a specific antigenic site on the a-subunit are bound and quantified. The assay is performed as described by the manufacturer is (Wallac Oy, Turku, Finland).
The results cleariy show that immunological active single chain hCG is produced from both expression constructs and not from the control plasmid. Moreover, the amount of single chain hCG produced from JV158 (267 mU/ml) seems to be considerably higher than the amount produced from JV10PSA (4.9 mU/ml), ao suggesting that in this case the human (3-hCG leader peptide is more effective then the Dictyostelium leader peptide from PsA.
The kinetics of single chain hCG production were studied for JV158 transformed cells. Different densities of transformed cells were seeded on plates in axenic media, 25 grown to confluence and maintained for several days, without any medium change.
An aliquot of medium was taken every 24 hrs and analyzed for the presence of single chain hCG. The expression-level reaches a maximum 4 to 5 days after cells reach confluence (data not shown). Since the cells start to detach from the plate at about 6-7 days after reaching confluence, medium was harvested at day 5 after reaching 3 o confluence.

Example 3:
Activity of single chain hCG expressed in Dictyostelium The ability of single chain hCG froiri Dictyostelium to bind to the human LH/CG
receptor was determined by a competitive binding assay with heterodimer hCG.
CHO
s cells expressing the human LH/CG receptor (Jia, X.-C. et al. (1991) Mol.
Endocrinol.
~, 759-7G8) were simultaneously incubated with 'ZSI-hCG and purified material from the cell culture supernatant of Dictyostelium.
The receptor-binding activity of purified single chain hCG was quantified with a radioligand receptor displacement assay on membrane fractions isolated from io exponentially growing cells. In a total volume of 0.5 ml buffer {final composition 10 mM Tris-HCI, 5 mM MgCl2, 0.1 % bovine serum albumin, pH 7.4) a fixed amount of membrane protein was incubated with 'ZSI-hCG (20,000 epm, approximately 12 pM) and increasing amounts of competitor protein for 18 hours at ambient temperature.
'ZSI_labelled hCG (NEX-lOG) was obtained from Du Pont de Nemours. Specific is binding was 10-12% of the total radioactivity added. After incubation bound and free hormone were separated by centrifugation. Highly purified, recombinant gonadotropins were used as standards.
For purification of hCG from Dictyostelium cell culture medium was harvested from large (22 x 22cm) culture plates. Purification was performed with the aid of a zo progran unable FPLC system (Pharmacia, Roosendaal, The Netherlands) using the control and chromatography supervision system UNICORN (Pharmacia, Roosendaal, The Netherlands). Purification of single chain hCG was accomplished using a combination of hydrophobic interaction and immuno chromatography with LH/CG (3-subunit specific monoclonal antibodies. For this purpose, 150 mls of medium were zs produced with a single chain hCG content of 0.372 unit/ml as determined by DELFIA~. Using this medium, approximately 3 units of purified single chain hCG
(~5% yield) were obtained. All procedures were carried out 4°C.
Coincubation with varying concentrations of wildtype hCG, wildtype hLH or single chains hCG displaced 'ZSI-hCG binding in a dose-dependent manner (Fig. 2). The 3o displacement curves indicate the material produced by Dictyostelium is indeed able to bind to the human LH/CG receptor. The affinity for the receptor is comparable to the affinity of single chain hCG produced by CHO cells, which has been shown to be considerably less effective in displacing 'ZSI-hCG binding than the heterodimer of hCG.~'Thus, there seems to be no significant difference in binding capacity between single chain hCG produced in Dictyostelium compared to CHO cells.
The bioactivity of single chain hCG from Dictyostelium was analyzed by s examination of its ability to stimulate cAMP production in CHO cells expressing the human LH/CG receptor. Cells were incubated for 4 hours with increasine concentrations of hormone in the presence of 0.1 mM 3-isobutyl-1-methylxanthin.
The extracellular CAMP was determined by RIA (Immunotech).
The results demonstrate that the single chain hCG produced by Dictyostelium is io indeed able to activate the human LH/CG receptor which results in the production of cAMP. Only a small difference in potency was observed between single chain hCG
produced in Dictyostelium compared to the material produced in CHO cells (ICso value approximately five-fold lower.
is Exam,pte Expression and bioactivity of heterodimeric hCG in Dictyostelium We aimed for the expression of heterodimeric hCG in Dictyostelium. For the expression of the a- and (3-subunits of hCG, two plasmids were generated.
Their structure and overall organisation is essentially identical to that of MBl2n which has so been described in example 1. In order to facilitate expression of two independent plasmids in Dd we replaced the blasticidine resistance cassette in MBI2n with the 2.4 kb KpnI-XbaI fragment from p155d1 (Hughes, J.E. et al. (1994) Mol. Cell.
Biol.. ~, 6117-6124) containing a neomycin cassette, creating MB l2neo. For the construction of the expression vector for the a-subunit, its natural cDNA sequence was produced by 25 PCR using primers which introduce a BgIII restriction site both at the 5' and 3' end of the fragment, so that it could be cloned in MB l2neo. For the conshuction of the expression vector for the (3-subunit of hCG, MBl2n was modified to contain another unique restriction site (SphI) 3' in the BgIII cloning site [see example 1].
The hCG (3-subunit cDNA was amplified using a 5' primer resulting in the alteration of the first 30 s o bases of the coding sequence conform the Dictyostelium preferred codon usage [see example 1 ]. The primers also introduced appropriate restriction sites at both the S' (BgIII) and 3' (SphI) end of the fragment to facilitate directional cloning.

The two expression plasmids were transformed simultaneously to Dictyostelium.
After transformation, cells were plated to clonal dilution. Clonal transformants were then selected and further grown for analysis. The amount of hCG secreted by Dictyostelium was determined as described by the manufacturer using a DELFIA~
hLH
s assay (Wallac Oy, Turku, Finland), which has a 100% cross-reactivity with hCG. The results clearly show that immunologically active hCG is indeed produced by Dictyostelium Although the presence of heterodimeric hCG was demonstrated in the medium by means of epitope detection, additional experiments were necessary to establish io whether hCG produced by Dictyostelium is biologically active.
Quantification was based on immuno-reactivity. The bioactivity of heterodimeric hCG from Dictyostelium was analysed by examination of its ability to activate the human LH/CG receptor in a luciferase reporter assay. The results demonstrate that the heterodimeric hCG produced by Dictyostelium is indeed able to activate the human is LH/CG receptor (Figure 4). Moreover, its bioactivity is comparable (ICS° value approximately two-fold higher) to the bioactivity of wildtype hCG produced by CHO
cells.
zo Expressio~z and bioactivity of heterodimeric FSH in Dictyostelium To investigate if Dictyostelium is also capable to produce other complex glycoprotein hormones, we studied the production of FSH in this organism. In line with the strategy for hCG (example 4), two expression plasmids were generated. For the construction of the expression vector for the (3-subunit of FSH, the cDNA was amplified z5 using a 5' primer resulting in the alteration of the first 27 bases of the coding sequence conform the Dictyostelium preferred codon usage and cloning was performed as described for the (3-subunit of hCG. After transformation of Dictyostelium, cells were plated to clonal dilution. Clonal transformants were then selected and fiuther grown for analysis.
3 o The amount of FSH secreted by Dictyostelium was determined by a sandwich immunoassay [SS-artikel]. The results demonstrate that immunological active FSH is produced by Dictyostelium. Moreover, heterodimeric FSH produced by Dictyostelium is also able to activate the human FSH receptor (Figure 5).

Example 66:
Random mutagenesis of a selected region of hCG in Dictyostelium Since we showed that Dictyostelium is capable of producing biologically active s gonadotropins, we aimed for the development of a random mutagenesis approach. For this purpose, we selected two amino acids in the determinant loop of hCG which have been demonstrated to be involved in receptor binding and signal transduction.
Specific base substitutions were introduced by site-specific mutagenesis and combining PCR-fragments that overlap in sequences as described using standard PCR
io conditions. The primers were designed to alter aminoacids 94 and 95 of the (3-subunit of hCG. The first two nucleotides of both codons were altered fully random (A,C,T
or G), while the third base was restricted to G or T to minimise to percentage of stopcodons introduced. The PCR fragments were separated and subcloned in pCR~ 2.1 (Invitrogen, Leek, The Netherlands). The primers were chosen in such a way that the subcloned is PCR-fragments contained a BgIII site at the 5' end and a SphI site at the 3' end. After PCR and cloning, the pool of pCR~ 2.1 constructs was transformed to E.coli.
Subsequently, DNA was isolated from a pool of 200 transformants and after restriction digestion the BgIII/SphI mutated fragments were subcloned in MBl2n containing the BgIII and SphI site. After plating E.coli transfonnants of MB 12 plasmids containing the zo random mutmt fragments, 400 colonies were pooled and DNA was prepared.
Dictyostelium was transformed simultaneously with the expression vector for the a-subunit by electroporation. Selection with blasticidine (10 p,g/ml) was introduced hours after electroporation. The next day, cells were clonally diluted in 96 well plates using 4 fold dilutions and neomycin selection (10 pg/ml) was iniated. Medium was zs replaced every 3-4 days, maintaining selective conditions. Positive wells were identified 11-14 days after electroporation, and the transformation efEciency was estimated from the dilution series. Typically, about 500 transformants were obtained by electroporation of 10' cells with 1 p,g of both the hCG a and hCG (3 vectors. Single wells were then selected for furkher experiments. A single well contains 200 pl of medium.
Larger a o amounts of media for purification were harvested from large {22 x 22cm) culture plates.
The supernatants of 85 Dictyostelium clones were analysed for the presence of immuno- and bioactivity. As controls, several wildtype hCG producing clones and non-transformed Dictyostelium clones were present on the 96-well plates.
Concentrations of wildtype and mutant hCG were measured using a DELFIA~ hLH assay (Wallac Oy, Turku, Finland), which has a 100% cross-reactivity with hCG. Subsequently, the in vitro biological activity on the human LH/CG receptor was determined. Half of the 85 mutmts analysed, show B/I ratios varying from 0.35 to 1.05. Taking variations of 2 s single analyses into account, the activities of these mutants are considered to be comparable to wildtype hCG. Approximately 40% of the mutants show decreased B/I
ratio's. This could be anticipated, since the mutated aminoacids 94 and 95 have been shown to be involved in receptor binding and activation. The fact that 11 clones do not show any hCG production is probably due to interference of the altered aminoacids with io appropriate folding of the mutated (3-polypeptide and/or association with the a-subunit or the fact that not all clones contain both an a- and a (3-subunit expression construct.
Twenty clones with varying B/I ratios were selected for detailed analysis.
Selected clones were further grown on 6-well plates until confluence and cell culture supernatants were collected after 4 additional days. Four of the twenty clones is did not produce any detectable hCG. This is in agreement with the results for these clones in the initial screen. Among the other clones, the amount of hCG
produced varied considerably (116-2118 mU/ml). The cell culture supernatants were analysed for the presence of in vitro biological activity of hCG at a range of concentrations.
All mutants which showed B/I ratios in the range of wildtype hCG in the initial screen, also ao displayed a wildtype in vitro biological activity when analysed in more detail. The four supernatants that did not show any immunological activity, were also not able to activate the LH/CG receptor. Therefore, we conclude that these clones are not producing any hCG. Furthermore, all mutants with decreased B/I ratios in the initial screen indeed show a clear increase in ICS. Their B/I ratios vary from a 2 fold to >100 fold lower than 2s wildtype hCG produced by Dictyostelium. The dose/response curves for eight of the mutants are shown in Figure 6.
To correlate the observed biological activities with the mutations present in the ~i-subunit, the mutated expression vectors were sequenced. We isolated total DNA
from selected Dictyostelium clones and transformed it to E.coli. For each Dictyostelium ao clone a number of transformants was analysed by colony-PCR for the presence of the a-subunit plasmid or the (3-subunit plasmid. Subsequently, DNA was isolated from several transformants containing the (3-subunit plasmid and sequence analysis was performed on the mutated region using an automated sequencer (Pharmacia).

Thus, the majority of Dictyostelium clones contains only one type of mutation in the hCG(3 expression vector. These clones produce a single type of mutant.
In addition, we conclude that the majority of Dictyostelium clones analysed contain unrelated sequences on position 94 and 95 of the ~i-subunit, suggesting that the s mutagenesis has been random indeed.
Mass spectrometric analysis of rec hCG from Dictyostelium discoideum Recombinant hCG, produced by Dictyostelium was isolated from culture io supernatant by subsequently hydrophobic interaction chromatography and immunochromatography with MoAb 119A that reacts with an epitope common to LH
and hCG. The antibody was immobilised to NHS-Sepharose. The acid-eluted, purified rec hCG was dialysed against 50% acetonitrile and lyophilised. The protein was dissolved in 0.1 % TFA and mass spec analysis was carried out with MALDI-TOF
i5 using superDHB as matrix. Pure rec hCG produced by CHO cells and isolated with the same purification procedure was used as a reference.
Both a- and (3- subunits of the Dictyostelium material were of lower molecular weight than the corresponding subunits from CHO cells , the median values of the peaks being 11578 and 17351 D for the Dictyostelium subunits and 14013 and ao D for the CHO polypeptides. This observation indicates that less and/or shorter carbohydrate chains are present on the Dicyostelium-produced hormone.
Moreover, the peak width of the corresponding subunits differed considerably i.e. 11110-D ( 1342 D) for the Dictyostelium a- vs 12959-15591 D (2632 D) for the CHO a-chain and 17006-18104 D (1098 D) for the Dictyostelium (3 vs 20674-25208 D
(4534 25 D) for the CHO ø-chain. This indicates that the glycosylation of the Dictyostelium product is far less complex.

Claims (7)

CLAIMS:

1. A gonadotropin or a mutant thereof obtainable by heterologous expression in a Dictyostelium host.

2. The mutant gonadotropin of claim 1 characterized in that the subunits are covalently linked.

3. The gonadotropin according to claims 1 or 2 for use as a therapeutical substance.

4. The gonadotropin according to claims 1-3 characterized in that said gonadotropin is hCG or FSH.

5. A pharmaceutical composition comprising the gonadotropin according to claims 1 or 2 and a pharmaceutical acceptable carrier.

6. A method for producing a gonadotropin or a mutant thereof comprising the steps of:
- transforming a strain of Dictyostelium with a recombinant plasmid vector comprising a DNA sequence encoding the gonadotropin genes or mutated genes under control of Dictyostelium regulatory sequences - culturing the recombinant strain under conditions to allow expression of the DNA sequence and - isolating of the expressed protein.

7. A method for selecting a gonadotropin mutant with super agonistic or antagonistic properties comprising the steps of:
- random mutagenesis of gonadotropin genes - insertion of the mutated genes in a Dictyostelium plasmid vector - transforming a strain of Dictyostelium with said recombinant plasmid vector - culturing clones under conditions to allow expression of the DNA sequence - determining the receptor binding / signal transduction ratio of the expressed protein - isolating clones with a ratio deviating from the ratio determined for wild type gonadotropins.