METHOD FOR PRODUCTION OF RECOMBINANT HUMAN THROMBIN

Abstract

The present invention relates to a method is provided for producing recombinant human thrombin from recombinant prothrombin using recombinant ecarin having the sequence SEQ ID NO 2 or a homologue thereof.

Description

CROSS REFERENCE TO RELATED APPLICATIONS

This application is a continuation (and claims the benefit of priority under 35 U.S.C. §120) of U.S. application Ser. No. 12/167,614, filed Jul. 3, 2008, which claims the benefit under 35 U.S.C. §119(e) of U.S. Provisional Application No. 60/948,207 (US) filed on Jul. 6, 2007, both of which are incorporated herein by reference in their entirety.

TECHNICAL FIELD

The present application relates to a method for producing recombinant human thrombin from recombinant prothrombin using recombinant ecarin.

BACKGROUND OF THE INVENTION

Thrombin is a key enzyme in the coagulation cascade. By thrombin mediated proteolytic digestion of fibrinogen into fibrin monomer, a cascade reaction leading to clot formation is started. Clot formation is the first step in wound healing. In addition thrombin is a chemo attractant to cells involved in wound healing, and, the fibrin network formed act as a scaffold for collagen-producing fibroblasts, increases phagocytosis, promotes angiogenesis and binds growth factors thus further supporting the healing process. The rate of clot formation is dependent on the concentration of thrombin and fibrinogen. Because of the important function in clot formation thrombin has been utilised in a number of products intended for haemostasis and/or as tissue sealants or “glues”, both as stand-alone products (i.e. Thrombin-JMI) or in combination with fibrin or other compounds (i.e. Tisseel, Hemaseel, Crosseal). The potential fields of use are numerous; skin grafting, neuro surgery, cardiac surgery, toracic surgery, vascular surgery, oncologic surgery, plastic surgery, ophthalmologic surgery, orthopedic surgery, trauma surgery, head and neck surgery, gynecologic and urologic surgery, gastrointestinal surgery, dental surgery, drug delivery, tissue engineering and dental cavity haemostasis.

So far the thrombin in approved thrombin-containing products on the market is derived either from human or bovine plasma. Using plasma derived protein confers several disadvantages as limited availability and safety concerns such as risk for transmission of viruses and prions and the risk of triggering autoantibody formation (bovine products). Cases where antibody formation due to bovine thrombin exposure has lead to significant bleeding disorders are known.

In vivo thrombin is obtained from activation of prothrombin through the coagulation cascade. Activation through the coagulation cascade is dependent on the presence of a functional GLA-domain containing 8-10 glutamic residues converted to gamma-carboxyglutamate. In vitro, also incomplete gamma-carboxylated prothrombin can be converted to thrombin by the use of prothrombin activators such as ecarin. Ecarin, a snake venom derived from the Kenyan viper Echis carinatus is a procoagulant, a protease which cleaves human prothrombin between residues Arg₃₂₀-IIe₃₂₁ to generate meizothrombin. Further autocatalytic processing results in the formation of meizothrombin desF1 and then alpha-thrombin, which is the mature active form of thrombin.

An ideal commercial thrombin manufacturing process would use a recombinant thrombin precursor and a recombinant protease produced at high productivity without addition of animal-derived components. Further requirements would be robust performance, convenience and low cost.

A big obstacle for efficient recombinant human thrombin (rh-thrombin) has been to obtain high yields of prothrombin. Although extensive efforts have been spent, obtaining high yields of prothrombin under conditions suitable for production of biologicals has long remained a challenge. Yonemura et al. (J Biochem 135:577-582, 2004) have used recombinant GLA-domain-less prethrombin digested with recombinant ecarin to generate recombinant human thrombin. The productivity of prethrombin at process scale was 150-200 mg/L, which is a modest productivity for commercial scale production. Recombinant production of ecarin has also been described in WO 01/04146. In this publication generation of rh-thrombin is exemplified by conversion of recombinant prothrombin produced in COS cells by a recombinant ecarin produced from CHO cells. However, the exemplified methods are not suitable for large-scale production and animal-derived components are used.

Recombinant ecarin is produced as a prepro-protein that needs to be activated. Problems to efficiently activate the r-ecarin are described in both publications and the suggested activation procedures are far from optimal.

Thus there is a need for improved methods to obtain recombinant human thrombin. During our efforts to obtain improved productivity of gamma-carboxylated human prothrombin we made the surprising discovery that co-expression with gamma-glutamyl carboxylase (GGCX) vastly improved also the productivity of incompletely carboxylated prothrombin (see WO2005038019).

The present invention describes a process to efficiently produce human thrombin from recombinant prothrombin obtained by the expression method as described in WO2005038019. Recombinant carboxylated or incompletely carboxylated prothrombin combined with recombinant ecarin has not previously been used for manufacturing of recombinant thrombin. Further, the procedure for activating recombinant ecarin is new. The methods described would be suitable for large scale rh-thrombin manufacturing without the addition of animal-derived components.

SUMMARY OF THE INVENTION

According to a first aspect of the invention, a method is provided for producing recombinant human thrombin from recombinant prothrombin using recombinant ecarin having the sequence SEQ ID NO 2 or a homologue thereof.

According to a another aspect, a pharmaceutical composition is provided comprising a recombinant thrombin according to said method, in combination with pharmaceutically acceptable carriers, vehicles and/or adjuvants.

According to further aspect, an isolated DNA sequence is provided coding for recombinant ecarin according to SEQ ID NO 2 or a homologue thereof, having at least 80% identity to SEQ ID NO 2.

According to another aspect, a vector is provided comprising an isolated DNA sequence coding for recombinant ecarin according to SEQ ID NO 2 or a homologue thereof, having at least 80% identity to SEQ ID NO 2.

According to yet another aspect, a cell line is provided comprising a vector comprising an isolated DNA sequence coding for recombinant ecarin according to SEQ ID NO 2 or a homologue thereof, having at least 80% identity to SEQ ID NO 2.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1. FII+GGCX construct (SEQ ID NO:1).

FIG. 2. Ecarin construct (SEQ ID NO:3).

FIG. 3. Example of a process outline for thrombin manufacturing.

FIGS. 4A-4C. Nucleotide sequence alignment of the nucleic acid sequence encoding recombinant ecarin (SEQ ID NO:2) used in the present invention and wild type ecarin nucleic acid sequence (SEQ ID NO:4).

FIG. 5. Amino acid sequence alignment of recombinant ecarin (encoded by SEQ ID NO:2) used in the present invention and wild type ecarin (both having the amino acid sequence of SEQ ID NO:5).

FIG. 6. Graph showing the activation of recombinant ecarin during cell death over time.

FIG. 7. Activation of recombinant ecarin in cell cultures over time, assayed by SDS-PAGE.

FIG. 8. Chromatogram from CIEX purification of rh-thrombin.

FIG. 9. Non-reduced SDS-PAGE analyses of fractions obtained by CIEX purification.

DETAILED DESCRIPTION OF THE INVENTION

The invention consists in one part of a cell line derived by stable transfection with a vector (FIG. 1) encoding human prothrombin (FII) associated by suitable control sequences and human gamma-glutamyl carboxylase (GGCX) associated by suitable control sequences. Control sequences should be chosen so that prothrombin expression is in excess of the GGCX expression by at least a factor of 10. The host cell is preferably a eukaryotic cell. Typical host cells include, but are not limited to insect cells, yeast cells, and mammalian cells. Mammalian cells are particularly preferred. Suitable mammalian cells lines include, but are not limited to, CHO, HEK, NS0, 293, Per C.6, BHK and COS cells, and derivatives thereof. In one embodiment the host cell is the mammalian cell line CHO-S. The obtained prothrombin producing cell line is grown under culture conditions optimised for high yield of prothrombin disregarding gamma-carboxylation. Vitamin K may or may not be added to the growth medium.

It will be appreciated that the invention is not restricted to a particular prothrombin or gamma-glutamyl caboxylase or protein encoding sequence of one of these proteins to be co-expressed. Moreover, and in particular with respect to blood coagulation factors, numerous mutant forms of the proteins have been disclosed in the art. The present invention is equally applicable to prothrombin and gamma-glutamyl caboxylase mutant forms, including naturally occurring allelic variants, of the proteins as it is to wild-type sequence. In one embodiment the invention can be undertaking with any wild-type protein or one with at least 90%, preferably at least 95% sequence identity thereto. In another embodiment, sequences listed in Table 1 can be used.

TABLE 1
	CDNA	SPLICE		GENE
	EMBL	VARIANTS		EMBL
PROTEIN	ACC#	(PROTEIN)	MUTATIONS	ACC#
Glutamate	BC013979	2; BC013979;	1 SNP	U65896
gamma		AF253530	(EMBL#
carboxylase			U65896);
			2 SNPs
			(OMIM#
			137167)
Prothrombin	V00595	1; V00595	approx. 100	AF478696
			SNP's
			(EMBL#
			AF478696)

Each of these proteins, including their nucleic acid and amino acid sequences, are well known. Table 2 identifies representative sequences of wild-type and mutant forms of the various proteins that can be used in the present invention.

The term “gamma-glutamyl carboxylase” or “GGCX”, as used herein, refers to a vitamin K dependent enzyme that catalyses carboxylation of glutamic acid residues.

GGCX enzymes are widely distributed, and have been cloned from many different species such as the beluga whale Delphinapterus leucas, the toadfish Opsanus tau, chicken (Gallus gallus), hagfish (Myxine glutinosa), horseshoe crab (Limulus polyphemus), and the cone snail Conus textile (Begley et al., 2000, ibid; Bandyopadhyay et al. 2002, ibid). The carboxylase from conus snail is similar to bovine carboxylase and has been expressed in COS cells (Czerwiec et al. 2002, ibid). Additional proteins similar to GGCX can be found in insects and prokaryotes such as Anopheles gambiae, Drosophila melanogaster and Leptospira with NCBI accession numbers: gi 31217234, gi 21298685, gi 24216281, gi 24197548 and (Bandyopadhyay et al., 2002, ibid), respectively. The carboxylase enzyme displays remarkable evolutionary conservation. Several of the non-human enzymes have shown, or may be predicted to have, activity similar to that of the human GGCX we have used, and may therefore be used as an alternative to the human enzyme.

Table 2 identifies representative sequences of predicted proteins homologous to human GGXC (sorted after species origin) that can be used in the present invention.

TABLE 2
                                 Data base accession
Species                          #/ID
Homo sapiens (man)               NM_000821.2
                                 HUMGLUCARB
                                 HUMHGCA
                                 BC004422
                                 HSU65896
                                 AF253530.1
Papio hamadryas (red baboon)     AC116665.1
Delphinapterus leucas (white whale) AF278713
Bos taurus (bovine)              NM_174066.2
                                 BOVCARBOXG
                                 BOVBGCA
Ovis aries (domestic sheep)      AF312035
Rattus norvegicus (brown rat)    NM_031756.1
                                 AF065387
Mus musculus (mouse)             NM_019802.1
                                 AF087938
Opsanus tau (bony fishes)        AF278714.1
Conus textile (molluscs)         AY0044904.1
                                 AF382823.2
Conus imperialis (molluscs)      AF448234.1
Conus episcopatus (molluscs)     AF448233.1
Conus omaria (molluscs)          AF448235.1
Drosophila melanogaster (fruit fly) NM_079161.2
Anopheles gambiae (mosquito)     XM_316389.1
Secale cereale (monocots)        SCE314767
Triticum aestivum (common wheat) AF280606.1
Triticum urartu (monocots)       AY245579.1
Hordeum vulgare (barley)         BLYHORDCA
Leptospira interrogans (spirochetes) AE011514.1
Streptomyces coelicolor (high GC Gram+ SCO939109
bacteria)                        SCO939124
                                 AF425987.1
Streptomyces lividans (high GC Gram+ bacteria) SLU22894
Streptomyces viginiae (high GC Gram+ bacteria) SVSNBDE
Micrococcus luteus (high GC Gram+ bacteria) MLSPCOPER
Chlamydomonas reinhardtii (green algae) AF479588.1
Dictyostelium discoideum (slime mold) AC115612.2
Coturnix coturnix (birds)        AF364329.1
Bradyrhizobium japonicum (α-protoebacteria) AP005937.1
Rhodobacter sphaeroides (α-proteobacteria) RSY14197
Sinorhizobium meliloti (α-proteobacteria) RME603647
                                 AF119834
Mesorhizobium loti (α-proteobacteria) AP003014.2
Chromobacterium violaceum (β-proteobacteria) AE016910.1
                                 AE016918.1
Pseudomonas aeruginosa (γ-proteobacteria) AE004613.1
                                 AF165882
Xanthomonas axonopodis(γ-proteobacteria) AE011706.1
Human herpesvirus 8              KSU52064
                                 KSU75698
                                 AF305694
                                 AF360120
                                 AF192756

Each of the above-identified GGCX proteins and GGCX proteins from other species can be used as the carboxylase enzyme in the present invention.

A second part of the invention is a cell line stably transfected with a polynucleotide encoding ecarin and associated control elements (FIG. 2). The ecarin encoding sequence may be optimised for expression in mammalian cells, but is not limited to such sequences. In one embodiment of the invention the sequence according to SEQ ID NO 2 or a homologue thereof is used to express ecarin. A homologue of

SEQ ID NO 2 coding for ecarin may have at least 80%, 85%, 90%, 95%, 97%, 98% or 99% identity to the sequence SEQ ID NO 2. The host cell is preferably a eukaryotic cell. Typical host cells include, but are not limited to insect cells, yeast cells, and mammalian cells. Mammalian cells are particularly preferred. Suitable mammalian cells lines include, but are not limited to, CHO, HEK, NS0, 293, Per C.6, BHK and COS cells, and derivatives thereof. In one embodiment the host cell is the mammalian cell line CHO-S.

In one embodiment prothrombin and ecarin are produced from cells originating from the same parent cell line. This cell line origin may be, but is not limited to, Chinese Hamster Ovary cells (CHO) including derivatives and NSO (myeloma BALB/c mouse) including derivatives. The purpose of using the same cell line background is to facilitate purification and evaluation of purity of the thrombin product.

In another embodiment ecarin and prothrombin are produced from different host cell line; i.e. CHO and NSO, respectively.

In one aspect of the invention use of recombinant ecarin is preferred as this facilitates detection of non-thrombin product derived components during the thrombin generation process and in the final thrombin product. In a second aspect recombinant ecarin is preferred due to reduced risk for exposure to allergenic or toxic components that may be present in ecarin derived from snake venom. In a third aspect ecarin from snake venom is not preferred due to batch variation and limited batch size of ecarin preparations.

The crude prothrombin and the crude ecarin are mixed and incubated under conditions that allow formation of thrombin, such as described in Example 3. Generated thrombin is then purified by methods described in Example 4 or by other methods known by persons skilled in the art. Alternatively prothrombin and/or ecarin can first be purified by methods known in the art and then mixed to obtain thrombin. Thrombin is then purified from non-product components.

An example of a suitable thrombin manufacturing process is outlined in FIG. 3.

A method is provided for producing recombinant human thrombin from recombinant prothrombin using recombinant ecarin having the sequence SEQ ID NO 2 or a homologue thereof. The recombinant ecarin can be expressed and secreted by a cell containing the gene comprising the nucleotide sequence SEQ ID NO 2 or a homologue thereof in CHO-S cells, which ecarin has an amino acid sequence equal to that of wild type ecarin.

In the above method the recombinant protrombin is subjected to recombinant ecarin, which recombinant ecarin can be isolated in active form after extra-cellular expression by CHO-S cells, said cells being left to apoptosis/necrosis for a time sufficient to activate said ecarin, whereupon a human recombinant thrombin is isolated.

The recombinant prothrombin can be produced by a cell-line comprising a prothrombin expressing gene having a nucleotide sequence comprising the sequence SEQ. ID. NO. 1 or an homologue thereof. A homologue of SEQ ID NO 1 coding for prothrombin may have at least 80%, 85%, 90%, 95%, 97%, 98% or 99% identity to the sequence SEQ ID NO 1. The recombinant prothrombin can be a mixture of fully carboxylated prothrombin and incompletely carboxylated prothrombin. In one embodiment, the recombinant prothrombin is a fully carboxylated prothrombin and in another embodiment, the recombinant prothrombin is an incompletely carboxylated prothrombin.

A further aspect of the invention relates to the recombinant thrombin obtained by the method according to the invention. A pharmaceutical composition can be designed comprising the recombinant thrombin obtained be the method according to the invention, in combination with pharmaceutically acceptable carriers, vehicles and/or adjuvants. The pharmaceutical composition can be in an applicable form.

In one embodiment thrombin produced by the described method can be used in the manufacturing of tissue sealants (“glues”) in combination with other proteins, i.e. fibrin originating from recombinant cells, transgenic animals or human plasma. In another embodiment thrombin produced by the described method can be used as a stand-alone product, freeze dried as single active component or in combination with a non-protein matrix, or, in solution as single active component or in combination with other active components.

Suitable mix-in components would be, but is not limited to, collagen, chitin, degradable polymers, cellulose, recombinant coagulation factors and fibrinogen from transgenic or recombinant sources.

The potential fields of use for the tissue sealants (“glues”) are numerous; skin grafting, neuro surgery, cardiac surgery, toracic surgery, vascular surgery, oncologic surgery, plastic surgery, ophthalmologic surgery, orthopedic surgery, trauma surgery, head and neck surgery, gynecologic and urologic surgery, gastrointestinal surgery, dental surgery, drug delivery, tissue engineering and dental cavity haemostasis.

A further aspect of the invention relates to a method for obtaining coagulation by administering a therapeutically effective amount of a recombinant human thrombin obtained using the method according to the invention to a patient.

Another aspect of the present invention is an isolated DNA sequence according SEQ ID NO 2 or homologues thereof coding for a recombinant ecarin. A homologue of SEQ ID NO 2 coding for ecarin may have at least 80%, 85%, 90%, 95%, 97%, 98% or 99% identity to the sequence SEQ ID NO 2. SEQ ID NO 2 is a designed sequence that has been optimised for optimal expression. The sequence is particularly suited for expression in mammalian cell systems.

According to another aspect a vector comprising SEQ ID NO 2 or a homologue thereof is provided. Said vector can be designed to overexpress SEQ ID NO 2 or a homologue thereof and is operably linked to expression control sequences permitting expression of ecarin encoded by SEQ ID NO 2 or a homologue thereof. According to a third aspect a host cell comprising said vector is provided that is capable of expressing ecarin encoded by SEQ ID NO 2 or a homologue thereof. This host cell is preferably a eukaryotic cell. Typical host cells include, but are not limited to insect cells, yeast cells, and mammalian cells. Mammalian cells are particularly preferred. Suitable mammalian cells lines include, but are not limited to, CHO, HEK, NSO, 293, Per C.6, BHK and COS cells, and derivatives thereof. In one embodiment the host cell is the mammalian cell line CHO-S.

According to another embodiment of the present invention a polypeptide comprising an amino acid sequence encoded by SEQ ID NO: 2 or a homologue thereof and obtained by the method described in Example 2.

The sequence identity between two sequences can be determined by pair-wise computer alignment analysis, using programs such as, BestFit, PILEUP, Gap or FrameAlign. The preferred alignment tool is BestFit. In practise, when searching for similar/identical sequences to the query search, from within a sequence database, it is generally necessary to perform an initial identification of similar sequences using suitable algorithms such as Blast, Blast2, NCBI Blast2, WashU Blast2, FastA, or Fasta3, and a scoring matrix such as Blosum 62. Such algorithms endeavour to closely approximate the “gold-standard” alignment algorithm of Smith-Waterman. Thus, the preferred software/search engine program for use in assessing similarity, i.e., how two primary polypeptide sequences line up is Smith-Waterman. Identity refers to direct matches, similarity allows for conservative substitutions.

Experimental Section

The invention will be further described by means of the following examples which shall not be interpreted as limiting the scope of the appended claims.

EXAMPLE 1

High Yield Production of Recombinant Human Prothrombin in CHO Cells

The P1E2 cell line containing the construct PN32 shown in FIG. 1 having the nucleotide sequence SEQ ID NO: 1, was grown in a fermentor according to the method described in WO2005038019, using a protein and animal component free growth medium in order to produce prothrombin for use in thrombin manufacturing. The cells were grown either by batch or perfusion culture methods (Table 1) and the amount of prothrombin produced was measured by an ecarin assay. This ecarin assay was performed essentially as the Chromogenix assay (Mölndal, Sweden) using purified plasma-derived human prothrombin (Haematologic Technologies Inc., Vermont, USA) as standard.

TABLE 1
Examples of yield of prothrombin in experimental fermentor runs
	Culture method &	Viable cells	Prothrombin
Experiment ID	time	(million cells/mL)	mg/L
CC2LC (272-8)	Batch, 238 h	5.9	281
CC2LD (272-8)	Batch, 238 h	6.2	276
326-11B	Perfusion, 259 h	18	722

The fermentor experiments showed that both batch and perfusion culture methods can be used to produce prothrombin suitable for production of recombinant thrombin (Table 1). The share of fully carboxylated prothrombin obtained in these fermentor runs was about 55-87%, the rest being incompletely carboxylated prothrombin.

EXAMPLE 2

Production of Recombinant Ecarin in CHO Cells

An ecarin encoding sequence having the nucleotide sequence SEQ ID NO: 2 optimised for expression in mammalian cells was synthesized and cloned into the Invitrogen vector pCDNA 3.1+(FIG. 2). An alignment of the nucleotide sequence of the recombinant ecarin used in the present invention to the sequence of wild type ecarin (GI:717090) is seen in FIG. 4. As can be seen in FIG. 5 this recombinant ecarin is 100% homologous to the amino acid sequence for wild type ecarin. This construct, AZ ecarin (SEQ ID NO. 3), was used to stably transfect CHO-S cells (Invitrogen). Ecarin is secreted by the host cell to the extra-cellular space, and in order to screen for ecarin producing clones, culture supernatant samples were removed and mixed with recombinant human prothrombin (rhFII) to a final concentration of 1 mg rhFII/L in assay buffer (50 mM Tris-HCl, pH 7.4 containing 0.1% BSA). This mix was incubated 20-40 minutes at 37° C. The thrombin generated by the action of ecarin present in the sample was then detected by adding a 1-2 mM solution of the chromogenic thrombin substrate S-2238 (Chromogenix, Mölndal). Colour development was monitored and stopped when suitable using 20% acetic acid. To estimate the activity of the recombinant ecarin produced, snake venom derived ecarin with a declared activity was purchased from Sigma and used as standard. The best producing cell line obtained produced up to 7000 U ecarin per litre culture in lab scale shaker cultures grown in animal component free medium.

Activation of Recombinant Ecarin

The above method produces the recombinant ecarin as a pro protein Thus, activation by removal of the pro-part is necessary for optimal activity. To our surprise, we found that activation was most conveniently obtained by continued incubation of the culture for at least 7 days after the death of the ecarin producing cells (FIG. 6). The culture medium used was CD-CHO supplemented with HT-supplement, non-essential amino acids and Glutamax I (as recommended by Invitrogen for CHO-S), and growth conditions were shaker bottles at 37° C. in an atmosphere containing 5% carbon dioxide. Culture samples were assayed for activity as described above. As can be seen from FIG. 6, the activity of recombinant ecarin increased during the activation period.

Samples from culture supernatants were also separated by SDS-PAGE and blotted to nitrocellulose mebranes. Labelling of the membrane was performed with polyclonal rabbit serum directed towards the mature part of ecarin expressed as inclusion bodies in E. coli. “M” indicates the molecular weight marker and numbers refer to day of sample collection. As can be seen from FIG. 7 the recombinant ecarin remains stable for more than a week after the death of the cells. Activation of ecarin may also take place at lower temperatures, for instance as low as room temperature, but will then require longer times for activation. Ecarin will remain stable for severable months in room temperature in the presence of dead host cells. The activity will increase gradually until it levels out. A decrease in activity has not been observed except in the presence of bacterial infections or high temperatures. Efforts to use trypsin for activation of ecarin were made, but were not successful.

EXAMPLE 3

Conversion of Prothrombin to Thrombin by Ecarin

The ecarin protease converts prothrombin to meizothrombin, an intermediate form of thrombin that has thrombin catalytic activity. Further processing into thrombin is achieved by auto-catalyses. To determine the estimated amount of ecarin culture needed for converting prothrombin into thrombin, we performed a series of test digests. Different amounts of ecarin-containing culture supernatants as obtained in Example 2, were mixed with 1 mg/ml prothrombin (as obtained in example 1) in PBS buffer (Cambrex). Incubation of the mixtures was done at 37° C. for 1-3 hours. Samples were then analysed by SDS-PAGE to identify the amount of recombinant ecarin needed for complete conversion of prothrombin into thrombin. By this procedure we found that the recombinant ecarin was very potent; one litre of ecarin culture supernatant at 7000 U/L is capable of complete conversion of 64 grams of prothrombin into thrombin in less than 3 hours at 37° C. Normally recombinantly produced prothrombin has to be purified in order to separate fully-carboxylated prothrombin from the incompletely carboxylated prothrombin. However this is not necessary for the present invention as the recombinant ecarin is able to efficiently activate both the fully carboxylated and the incompletely carboxylated prothrombins.

EXAMPLE 4

Purification of Thrombin

Thrombin obtained by the procedure described in example 3 was purified by cation-exchange chromatography (CIEX) using AKTA-FPLC (GE Healthcare) and an SP-Sepharose HP column (GE Healthcare) equilibrated with 25 mM sodium-phosphate buffer, pH 6.5. Ecarin-digested prothrombin prepared as in example 3 was adjusted to pH 6.2 and a conductivity of approximately 8 mS/cm. Thrombin was eluted with a 1M sodium chloride gradient in column equilibration buffer over 20 column volumes (FIG. 8). Selected fractions were analysed by SDS-PAGE (FIG. 9). Thrombin activity was confirmed by incubation with the chromogenic thrombin substrate S-2238 (Chromogenix, Mölndal).

EXAMPLE 5

Analyses of rh-thrombin Obtained

To further analyse the obtained thrombin, kinetic parameters were determined using the chromogenic thrombin substrate S-2366 (Chromogenix). Activity was estimated by titration with hirudin. The rh-thrombin was for all parameters; Activity, K_kat and V_max, similar to plasma-derived human a-thrombin from Haematologic Technologies Inc. (Vermont, USA).

Purified thrombin was also subjected to N-terminal sequencing: Reduced thrombin heavy and light polypeptide chains were separated by SDS-PAGE and blotted to Immobilon P membrane (Millipor). The excised bands were sequenced by the Edman degradation method. Heavy chain N-terminal first five amino acids were confirmed to be IVEGS, and the light chain five N-terminal amino acids were TFGS as expected.

Below are the sequences for SEQ ID NOS. 3, 2, and 1:

SEQ ID NO. 3
gacggatcgggagatctcccgatcccctatggtcgactctcagtacaatctgctctgatgccgcatagttaagccagtat
ctgctccctgcttgtgtgttggaggtcgctgagtagtgcgcgagcaaaatttaagctacaacaaggcaaggcttgaccg
acaattgcatgaagaatctgcttagggttaggcgttttgcgctgcttcgcgatgtacgggccagatatacgcgttgacatt
gattattgactagttattaatagtaatcaattacggggtcattagttcatagcccatatatggagttccgcgttacataactta
cggtaaatggcccgcctggctgaccgcccaacgacccccgcccattgacgtcaataatgacgtatgttcccatagtaa
cgccaatagggactttccattgacgtcaatgggtggactatttacggtaaactgcccacttggcagtacatcaagtgtat
catatgccaagtacgccccctattgacgtcaatgacggtaaatggcccgcctggcattatgcccagtacatgaccttat
gggactttcctacttggcagtacatctacgtattagtcatcgctattaccatggtgatgcggttttggcagtacatcaatggg
cgtggatagcggtttgactcacggggatttccaagtctccaccccattgacgtcaatgggagtttgttttggcaccaaaat
caacgggactttccaaaatgtcgtaacaactccgccccattgacgcaaatgggcggtaggcgtgtacggtgggaggt
ctatataagcagagctctctggctaactagagaacccactgcttactggcttatcgaaattaatacgactcactataggg
agacccaagctggctagcgtttaaacttaagcttggtaccgagctcggatccactagtccagtgtggtggaattctgca
gatatccaccatgatccagatcctgctggtgatcatctgcctggccgtgttcccctaccagggctgctccatcatcctggg
cagcggcaacgtgaacgactacgaggtggtgtacccccagaaggtgaccgccctgcccaagggcgccgtgcagc
agcccgagcagaaatacgaggacgccatgcagtacgagttcgaggtgaagggcgagcccgtggtgctgcacctg
gagaagaacaaggagctgttcagcgaggactacagcgagacccactacagcagcgacgacagggagatcacc
accaaccccagcgtggaggaccactgctactaccacggccggatccagaacgacgccgagagcaccgccagca
tcagcgcctgtaatggcctgaagggccacttcaagctgagaggcgagacctacttcatcgagcccctgaagatcccc
gacagcgaggcccacgccgtgtacaagtacgagaacatcgagaacgaggacgaggcccctaagatgtgtggcgt
gacccaggacaactgggagagcgacgagcccatcaagaaaaccctgggcctgatcgtgcccccccacgagaga
aagttcgagaagaagttcatcgaactggtggtcgtggtggaccacagcatggtgaccaagtacaacaacgacagca
ccgccatcaggacctggatctacgagatgctgaacaccgtgaacgagatctacctgcccttcaacatcagagtggcc
ctggtgggcctggagttctggtgtaacggcgacctgatcaacgtgaccagcaccgccgacgacaccctgcacagctt
cggcgagtggagagccagcgacctgctgaaccggaagagacacgatcacgcccagctgctgaccaatgtgaccc
tggaccactccaccctgggcatcaccttcgtgtacggcatgtgtaagagcgaccggagcgtggagctgatcctggact
acagcaacatcaccttcaacatggcctacatcatcgcccacgagatgggccacagcctgggcatgctgcacgacac
caagttctgtacctgtggcgccaagccctgtatcatgttcggcaaggagagcatccctccccctaaggagttcagcag
ctgctcctacgaccagtacaataagtacctgctgaagtacaaccccaagtgtatcctggacccccccctgagaaagg
acatcgccagccctgccgtgtgtggcaatgagatctgggaggagggcgaggagtgtgactgtggcagcccagccg
actgtagaaacccctgctgtgatgccgccacctgtaagctgaagcctggcgccgagtgtggcaacggcgagtgctgt
gacaagtgtaagatccggaaggccggcaccgagtgtagacccgccagggacgattgtgacgtggccgagcactgt
accggccagagcgccgagtgccccagaaacgagttccagaggaacggccagccttgcctgaacaacagcggct
actgctacaacggcgactgccccatcatgctgaaccagtgtatcgccctgttcagccccagcgccaccgtggcccag
gacagctgcttccagagaaacctgcagggcagctactacggctactgtaccaaggagatcggctactacggaaag
aggttcccctgtgcccctcaggacgtgaagtgtggcaggctgtactgcctggacaactccttcaagaaaaacatgagg
tgtaagaacgactacagctacgccgacgagaacaagggcatcgtggagcccggcaccaagtgtgaggacggca
aagtgtgtatcaaccggaagtgtgtggacgtgaacaccgcctactgatgagcggccgctcgagtctagagggcccgt
ttaaacccgctgatcagcctcgactgtgccttctagttgccagccatctgttgtttgcccctcccccgtgccttccttgaccct
ggaaggtgccactcccactgtcctttcctaataaaatgaggaaattgcatcgcattgtctgagtaggtgtcattctattctg
gggggtggggtggggcaggacagcaagggggaggattgggaagacaatagcaggcatgctggggatgcggtgg
gctctatggcttctgaggcggaaagaaccagctggggctctagggggtatccccacgcgccctgtagcggcgcatta
agcgcggcgggtgtggtggttacgcgcagcgtgaccgctacacttgccagcgccctagcgcccgctcctttcgctttctt
cccttcctttctcgccacgttcgccggctttccccgtcaagctctaaatcggggcatccctttagggttccgatttagtgcttt
acggcactcgaccccaaaaaacttgattagggtgatggttcacgtagtgggccatcgccctgatagacggtttttcgc
cctttgacgttggagtccacgttctttaatagtggactcttgttccaaactggaacaacactcaaccctatctcggtctattct
tttgatttataagggattttggggatttcggcctattggttaaaaaatgagctgatttaacaaaaatttaacgcgaattaattc
tgtggaatgtgtgtcagttagggtgtggaaagtccccaggctccccaggcaggcagaagtatgcaaagcatgcatctc
aattagtcagcaaccaggtgtggaaagtccccaggctccccagcaggcagaagtatgcaaagcatgcatctcaatt
agtcagcaaccatagtcccgcccctaactccgcccatcccgcccctaactccgcccagttccgcccattctccgcccc
atggctgactaattttttttatttatgcagaggccgaggccgcctctgcctctgagctattccagaagtagtgaggaggcttt
tttggaggcctaggcttttgcaaaaagctcccgggagcttgtatatccattttcggatctgatcaagagacaggatgagg
atcgtttcgcatgattgaacaagatggattgcacgcaggttctccggccgcttgggtggagaggctattcggctatgact
gggcacaacagacaatcggctgctctgatgccgccgtgttccggctgtcagcgcaggggcgcccggttctttttgtcaa
gaccgacctgtccggtgccctgaatgaactgcaggacgaggcagcgcggctatcgtggctggccacgacgggcgtt
ccttgcgcagctgtgctcgacgttgtcactgaagcgggaagggactggctgctattgggcgaagtgccggggcagga
tctcctgtcatctcaccttgctcctgccgagaaagtatccatcatggctgatgcaatgcggcggctgcatacgcttgatcc
ggctacctgcccattcgaccaccaagcgaaacatcgcatcgagcgagcacgtactcggatggaagccggtcttgtc
gatcaggatgatctggacgaagagcatcaggggctcgcgccagccgaactgttcgccaggctcaaggcgcgcatg
cccgacggcgaggatctcgtcgtgacccatggcgatgcctgcttgccgaatatcatggtggaaaatggccgcttttctg
gattcatcgactgtggccggctgggtgtggcggaccgctatcaggacatagcgttggctacccgtgatattgctgaaga
gcttggcggcgaatgggctgaccgcttcctcgtgctttacggtatcgccgctcccgattcgcagcgcatcgccttctatcg
ccttcttgacgagttcttctgagcgggactctggggttcgaaatgaccgaccaagcgacgcccaacctgccatcacga
gatttcgattccaccgccgccttctatgaaaggttgggcttcggaatcgttttccgggacgccggctggatgatcctccag
cgcggggatctcatgctggagttcttcgcccaccccaacttgtttattgcagcttataatggttacaaataaagcaatagc
atcacaaatttcacaaataaagcatttttttcactgcattctagttgtggtttgtccaaactcatcaatgtatcttatcatgtctgt
ataccgtcgacctctagctagagcttggcgtaatcatggtcatagctgtttcctgtgtgaaattgttatccgctcacaattcc
acacaacatacgagccggaagcataaagtgtaaagcctggggtgcctaatgagtgagctaactcacattaattgcgtt
gcgctcactgcccgctttccagtcgggaaacctgtcgtgccagctgcattaatgaatcggccaacgcgcggggagag
gcggtttgcgtattgggcgctcttccgcttcctcgctcactgactcgctgcgctcggtcgttcggctgcggcgagcggtatc
agctcactcaaaggcggtaatacggttatccacagaatcaggggataacgcaggaaagaacatgtgagcaaaag
gccagcaaaaggccaggaaccgtaaaaaggccgcgttgctggcgtttttccataggctccgcccccctgacgagca
tcacaaaaatcgacgctcaagtcagaggtggcgaaacccgacaggactataaagataccaggcgtttccccctgga
agctccctcgtgcgctctcctgttccgaccctgccgcttaccggatacctgtccgcctttctcccttcgggaagcgtggcg
ctttctcaatgctcacgctgtaggtatctcagttcggtgtaggtcgttcgctccaagctgggctgtgtgcacgaacccccc
gttcagcccgaccgctgcgccttatccggtaactatcgtcttgagtccaacccggtaagacacgacttatcgccactgg
cagcagccactggtaacaggattagcagagcgaggtatgtaggcggtgctacagagttcttgaagtggtggcctaac
tacggctacactagaaggacagtatttggtatctgcgctctgctgaagccagttaccttcggaaaaagagttggtagctc
ttgatccggcaaacaaaccaccgctggtagcggtggtttttttgtttgcaagcagcagattacgcgcagaaaaaaagg
atctcaagaagatcctttgatcttttctacggggtctgacgctcagtggaacgaaaactcacgttaagggattttggtcatg
agattatcaaaaaggatcttcacctagatccttttaaattaaaaatgaagttttaaatcaatctaaagtatatatgagtaaa
cttggtctgacagttaccaatgcttaatcagtgaggcacctatctcagcgatctgtctatttcgttcatccatagttgcctgac
tccccgtcgtgtagataactacgatacgggagggcttaccatctggccccagtgctgcaatgataccgcgagaccca
cgctcaccggctccagatttatcagcaataaaccagccagccggaagggccgagcgcagaagtggtcctgcaactt
tatccgcctccatccagtctattaattgttgccgggaagctagagtaagtagttcgccagttaatagtttgcgcaacgttgtt
gccattgctacaggcatcgtggtgtcacgctcgtcgtttggtatggcttcattcagctccggttcccaacgatcaaggcga
gttacatgatcccccatgttgtgcaaaaaagcggttagctccttcggtcctccgatcgttgtcagaagtaagttggccgca
gtgttatcactcatggttatggcagcactgcataattctcttactgtcatgccatccgtaagatgcttttctgtgactggtgagt
actcaaccaagtcattctgagaatagtgtatgcggcgaccgagttgctcttgcccggcgtcaatacgggataataccgc
gccacatagcagaactttaaaagtgctcatcattggaaaacgttcttcggggcgaaaactctcaaggatcttaccgctg
ttgagatccagttcgatgtaacccactcgtgcacccaactgatcttcagcatcttttactttcaccagcgtttctgggtgagc
aaaaacaggaaggcaaaatgccgcaaaaaagggaataagggcgacacggaaatgttgaatactcatactcttcct
ttttcaatattattgaagcatttatcagggttattgtctcatgagcggatacatatttgaatgtatttagaaaaataaacaaat
aggggttccgcgcacatttccccgaaaagtgccacctgacgtc//
SEQ ID NO. 2
atgatccagatcctgctggtgatcatctgcctggccgtgttcccctaccagggctgctccatcatcctgggcagcggcaa
cgtgaacgactacgaggtggtgtacccccagaaggtgaccgccctgcccaagggcgccgtgcagcagcccgagcagaaat
acgaggacgccatgcagtacgagttcgaggtgaagggcgagcccgtggtgctgcacctggagaagaacaaggagctgttc
agcgaggactacagcgagacccactacagcagcgacgacagggagatcaccaccaaccccagcgtggaggaccactgcta
ctaccacggccggatccagaacgacgccgagagcaccgccagcatcagcgcctgtaatggcctgaagggccacttcaagc
tgagaggcgagacctacttcatcgagcccctgaagatccccgacagcgaggcccacgccgtgtacaagtacgagaacatc
gagaacgaggacgaggcccctaagatgtgtggcgtgacccaggacaactgggagagcgacgagcccatcaagaaaaccct
gggcctgatcgtgcccccccacgagagaaagttcgagaagaagttcatcgaactggtggtcgtggtggaccacagcatgg
tgaccaagtacaacaacgacagcaccgccatcaggacctggatctacgagatgctgaacaccgtgaacgagatctacctg
cccttcaacatcagagtggccctggtgggcctggagttctggtgtaacggcgacctgatcaacgtgaccagcaccgccga
cgacaccctgcacagcttcggcgagtggagagccagcgacctgctgaaccggaagagacacgatcacgcccagctgctga
ccaatgtgaccctggaccactccaccctgggcatcaccttcgtgtacggcatgtgtaagagcgaccggagcgtggagctg
atcctggactacagcaacatcaccttcaacatggcctacatcatcgcccacgagatgggccacagcctgggcatgctgca
cgacaccaagttctgtacctgtggcgccaagccctgtatcatgttcggcaaggagagcatccctccccctaaggagttca
gcagctgctcctacgaccagtacaataagtacctgctgaagtacaaccccaagtgtatcctggacccccccctgagaaag
gacatcgccagccctgccgtgtgtggcaatgagatctgggaggagggcgaggagtgtgactgtggcagcccagccgactg
tagaaacccctgctgtgatgccgccacctgtaagctgaagcctggcgccgagtgtggcaacggcgagtgctgtgacaagt
gtaagatccggaaggccggcaccgagtgtagacccgccagggacgattgtgacgtggccgagcactgtaccggccagagc
gccgagtgccccagaaacgagttccagaggaacggccagccttgcctgaacaacagcggctactgctacaacggcgactg
ccccatcatgctgaaccagtgtatcgccctgttcagccccagcgccaccgtggcccaggacagctgcttccagagaaacc
tgcagggcagctactacggctactgtaccaaggagatcggctactacggaaagaggttcccctgtgcccctcaggacgtg
aagtgtggcaggctgtactgcctggacaactccttcaagaaaaacatgaggtgtaagaacgactacagctacgccgacga
gaacaagggcatcgtggagcccggcaccaagtgtgaggacggcaaagtgtgtatcaaccggaagtgtgtggacgtgaaca
ccgcctactga
SEQ ID NO. 1
gacggatcgggagatctcccgatcccctatggtgcactctcagtacaatctgctctgatgccgcatagttaagccagtat
ctgctccctgcttgtgtgttggaggtcgctgagtagtgcgcgagcaaaatttaagctacaacaaggcaaggcttgaccg
acaattgcatgaagaatctgcttagggttaggcgttttgcgctgcttcgcgatgtacgggccagatatacgcgttgacatt
gattattgactagttattaatagtaatcaattacggggtcattagttcatagcccatatatggagttccgcgttacataactta
cggtaaatggcccgcctggctgaccgcccaacgacccccgcccattgacgtcaataatgacgtatgttcccatagtaa
cgccaatagggactttccattgacgtcaatgggtggagtatttacggtaaactgcccacttggcagtacatcaagtgtat
catatgccaagtacgccccctattgacgtcaatgacggtaaatggcccgcctggcattatgcccagtacatgaccttat
gggactttcctacttggcagtacatctacgtattagtcatcgctattaccatggtgatgcggttttggcagtacatcaatggg
cgtggatagcggtttgactcacggggatttccaagtctccaccccattgacgtcaatgggagtttgttttggcaccaaaat
caacgggactttccaaaatgtcgtaacaactccgccccattgacgcaaatgggcggtaggcgtgtacggtgggaggt
ctatataagcagagctctctggctaactagagaacccactgcttactggcttatcgaaattaatacgactcactataggg
agacccaagctggctagcgtttaaacttaagcttggtaccgagctcggatccactagtccagtgtggtggaattgccctt
attcctcagtgacccaggagctgacacactatggcgcacgtccgaggcttgcagctgcctggctgcctggccctggct
gccctgtgtagccttgtgcacagccagcatgtgttcctggctcctcagcaagcacggtcgctgctccagcgggtccggc
gagccaacaccttcttggaggaggtgcgcaagggcaacctggagcgagagtgcgtggaggagacgtgcagctac
gaggaggccttcgaggctctggagtcctccacggctacggatgtgttctgggccaagtacacagcttgtgagacagc
gaggacgcctcgagataagcttgctgcatgtctggaaggtaactgtgctgagggtctgggtacgaactaccgagggc
atgtgaacatcacccggtcaggcattgagtgccagctatggaggagtcgctacccacataagcctgaaatcaactcc
actacccatcctggggccgacctacaggagaatttctgccgcaaccccgacagcagcaccacgggaccctggtgct
acactacagaccccaccgtgaggaggcaggaatgcagcatccctgtctgtggccaggatcaagtcactgtagcgat
gactccacgctccgaaggctccagtgtgaatctgtcacctccattggagcagtgtgtccctgatcgggggcagcagta
ccaggggcgcctggcggtgaccacacatgggctcccctgcctggcctgggccagcgcacaggccaaggccctga
gcaagcaccaggacttcaactcagctgtgcagctggtggagaacttctgccgcaacccagacggggatgaggagg
gcgtgtggtgctatgtggccgggaagcctggcgactttgggtactgcgacctcaactattgtgaggaggccgtggagg
aggagacaggagatgggctggatgaggactcagacagggccatcgaagggcgtaccgccaccagtgagtacca
gactttcttcaatccgaggacctttggctcgggagaggcagactgtgggctgcgacctctgttcgagaagaagtcgctg
gaggacaaaaccgaaagagagctcctggaatcctacatcgacgggcgcattgtggagggctcggatgcagagatc
ggcatgtcaccttggcaggtgatgcttttccggaagagtccccaggagctgctgtgtggggccagcctcatcagtgacc
gctgggtcctcaccgccgcccactgcctcctgtacccgccctgggacaagaacttcaccgagaatgaccttctggtgc
gcattggcaagcactcccgcaccaggtacgagcgaaacattgaaaagatatccatgttggaaaagatctacatcca
ccccaggcaagcactggcgggagaacctggaccgggacattgccctgatgaagctgaagaagcctgttgccttcagtg
actacattcaccctgtgtgtctgcccgacagggagacggcagccagcttgctccaggctggatacaaggggcgggtg
acaggctggggcaacctgaaggagacgtggacagccaacgttggtaaggggcagcccagtgtcctgcaggtggtg
aacctgcccattgtggagcggccggtctgcaaggactccacccggatccgcatcactgacaacatgttctgtgctggtt
acaagcctgatgaagggaaacgaggggatgcctgtgaaggtgacagtgggggaccctttgtcatgaagagcccctt
taacaaccgctggtatcaaatgggcatcgtctcatggggtgaaggctgtgaccgggatgggaaatatggcttctacac
acatgtgttccgcctgaagaagtggatacagaaggtcattgatcagtttggagagtagaagggcaattctgcagatatc
cagcacagtggcggccgctcgagtctagagggcccgtttaaacccgctgatcagcctcgactgtgccttctagttgcca
gccatctgttgtttgcccctcccccgtgccttccttgaccctggaaggtgccactcccactgtcctttcctaataaaatgag
gaaattgcatcgcattgtctgagtaggtgtcattctattctggggggtggggtggggcaggacagcaagggggaggat
tgggaagacaatagcaggcatgctggggatgcggtgggctctatggcttctgaggcggaaagaaccagctggggct
ctagggggtatccccacgcgccctgtagcggcgcattaagcgcggcgggtgtggtggttacgcgcagcgtgaccgct
acacttgccagcgccctagcgcccgctcctttcgctttcttcccttcctttctcgccacgttcgccggctttccccgtcaagct
ctaaatcgggggctccctttagggttccgatttagtgctttacggcaccttcgaccccaaaaaacttgattagggctgtgg
aatgtgtgtcagttagggtgtggaaagtccccaggctccccagcaggcagaagtatgcaaagcatgcatctcaattag
tcagcaaccaggtgtggaaagtccccaggctccccagcaggcagaagtatgcaaagcatgcatctcaattagtcag
caaccatagtcccgcccctaactccgcccatcccgcccctaactccgcccagttccgcccattctccgccccatggctg
actaattttttttatttatgcagaggccgaggccgcctcggcctctgagctattccagaagtagtgaggaggcttttttggag
gcctaggcttttgcaaaaagctctctggctaactagagaacccactgcttactggcttatcgaaattaatacgactcacta
tagggagacccaagctggctagcgtttaaacttaagcttggtaccgagctcggatccactagtccagtgtggtggaatt
gccctttccgcagagcaatggcggtgtctgccgggtccgcgcggacctcgcccagctcagataaagtacagaaaga
caaggctgaactgatctcagggcccaggcaggacagccgaatagggaaactcttgggttttgagtggacagatttgtc
cagttggcggaggctggtgaccctgctgaatcgaccaacggaccctgcaagcttagctgtctttcgttttctttttgggttctt
gatggtgctagacattccccaggagcgggggctcagctctctggaccggaaataccttgatgggctggatgtgtgccg
cttccccttgctggatgccctacgcccactgccacttgactggatgtatcttgtctacaccatcatgtttctgggggcactgg
gcatgatgctgggcctgtgctaccggataagctgtgtgttattcctgctgccatactggtatgtgtttctcctggacaagac
atcatggaacaaccactcctatctgtatgggttgttggcctttcagctaacattcatggatgcaaaccactactggtctgtg
gacggtctgctgaatgcccataggaggaatgcccacgtgcccctttggaactatgcagtgctccgtggccagatcttca
ttgtgtacttcattgcgggtgtgaaaaagctggatgcagactgggttgaaggctattccatggaatatttgtcccggcact
ggctcttcagtcccttcaaactgctgttgtctgaggagctgactagcctgctggtcgtgcactggggtgggctgctgcttga
cctctcagctggtttcctgctcttttttgatgtctcaagatccattggcctgttctttgtgtcctacttccactgcatgaattcccag
cttttcagcattggtatgttctcctacgtcatgctggccagcagccctctcttctgctcccctgagtggcctcggaagctggt
gtcctactgcccccgaaggttgcaacaactgttgcccctcaaggcagcccctcagcccagtgtttcctgtgtgtataaga
ggagccggggcaaaagtggccagaagccagggctgcgccatcagctgggagctgccttcaccctgctctacctcct
ggagcagctattcctgccctattctcattttctcacccagggctataacaactggacaaatgggctgtatggctattcctgg
gacatgatggtgcactcccgctcccaccagcacgtgaagatcacctaccgtgatggccgcactggcgaactgggcta
ccttaaccctggggtatttacacagagtcggcgatggaaggatcatgcagacatgctgaagcaatatgccacttgcct
gagccgcctgcttcccaagtataatgtcactgagccccagatctactttgatatttgggtctccatcaatgaccgcttcca
gcagaggatttttgaccctcgtgtggacatcgtgcaggccgcttggtcaccctttcagcgcacatcctgggtgcaacca
ctcttgatggacctgtctccctggagggccaagttacaggaaatcaagagcagcctagacaaccacactgaggtggt
cttcattgcagatttccctggactgcacttggagaattttgtgagtgaagacctgggcaacactagcatccagctgctgc
agggggaagtgactgtggagcttgtggcagaacagaagaaccagactcttcgagagggagaaaaaatgcagttgc
ctgctggtgagtaccataaggtgtatacgacatcacctagcccttcttgctacatgtacgtctatgtcaacactacagagc
ttgcactggagcaagacctggcatatctgcaagaattaaaggaaaaggtggagaatggaagtgaaacagggcctct
acccccagagctgcagcctctgttggaaggggaagtaaaagggggccctgagccaacacctctggttcagacctttc
ttagacgccaacaaaggctccaggagattgaacgccggcgaaatactcctttccatgagcgattcttccgcttcttgttg
cgaaagctctatgtctttcgccgcagcttcctgatgacttgtatctcacttcgaaatctgatattaggccgtccttccctgga
gcagctggcccaggaggtgacttatgcaaacttgagaccctttgaggcagttggagaactgaatccctcaaacacgg
attcttcacattctaatcctcctgagtcaaatcctgatcctgtccactcagagttctgaagggggccagatgttggaaggg
caattcgagtctagagggcccgccctgatagacggtttttcgccctttgacgttggagtccacgttctttaatagtggactct
tgttccaaactggaacaacactcaaccctatctcggtctattcttttgatttataagggattttgccgatttcggcctattggtt
aaaaaatgagctgatttaacaaaaatttaacgcgaattaattctgtggaatgtgtgtcagttagggtgtggaaagtcccc
aggctccccagcaggcagaagtatgcaaagcatgcatctcaattagtcagcaaccaggtgtggaaagtccccaggc
tccccagcaggcagaagtatgcaaagcatgcatctcaattagtcagcaaccatagtcccgcccctaactccgcccat
cccgcccctaactccgcccagttccgcccattctccgccccatggctgactaattttttttatttatgcagaggccgaggcc
gcctctgcctctgagctattccagaagtagtgaggaggcttttttggaggcctaggcttttgcaaaaagctcccgggagc
ttgtatatccattttcggatctgatcaagagacaggatgaggatcgtttcgcatgattgaacaagatggattgcacgcag
gttctccggccgcttgggtggagaggctattcggctatgactgggcacaacagacaatcggctgctctgatgccgccgt
gttccggctgtcagcgcaggggcgcccggttctttttgtcaagaccgacctgtccggtgccctgaatgaactgcaggac
gaggcagcgcggctatcgtggctggccacgacgggcgttccttgcgcagctgtgctcgacgttgtcactgaagcggg
aagggactggctgctattgggcgaagtgccggggcaggatctcctgtcatctcaccttgctcctgccgagaaagtatcc
atcatggctgatgcaatgcggcggctgcatacgcttgatccggctacctgcccattcgaccaccaagcgaaacatcgc
atcgagcgagcacgtactcggatggaagccggtcttgtcgatcaggatgatctggacgaagagcatcaggggctcg
cgccagccgaactgttcgccaggctcaaggcgcgcatgcccgacggcgaggatctcgtcgtgacccatggcgatgc
ctgcttgccgaatatcatggtggaaaatggccgcttttctggattcatcgactgtggccggctgggtgtggcggaccgct
atcaggacatagcgttggctacccgtgatattgctgaagagcttggcggcgaatgggctgaccgcttcctcgtgctttac
ggtatcgccgctcccgattcgcagcgcatcgccttctatcgccttcttgacgagttcttctgagcgggactctggggttcga
aatgaccgaccaagcgacgcccaacctgccatcacgagatttcgattccaccgccgccttctatgaaaggttgggctt
cggaatcgttttccgggacgccggctggatgatcctccagcgcggggatctcatgctggagttcttcgcccaccccaac
ttgtttattgcagcttataatggttacaaataaagcaatagcatcacaaatttcacaaataaagcatttttttcactgcattct
agttgtggtttgtccaaactcatcaatgtatcttatcatgtctgtataccgtcgacctctagctagagcttggcgtaatcatgg
tcatagctgtttcctgtgtgaaattgttatccgctcacaattccacacaacatacgagccggaagcataaagtgtaaagc
ctggggtgcctaatgagtgagctaactcacattaattgcgttgcgctcactgcccgctttccagtcgggaaacctgtcgtg
ccagctgcattaatgaatcggccaacgcgcggggagaggcggtttgcgtattgggcgctcttccgcttcctcgctcact
gactcgctgcgctcggtcgttcggctgcggcgagcggtatcagctcactcaaaggcggtaatacggttatccacagaa
tcaggggataacgcaggaaagaacatgtgagcaaaaggccagcaaaaggccaggaaccgtaaaaaggccgc
gttgctggcgtttttccataggctccgcccccctgacgagcatcacaaaaatcgacgctcaagtcagaggtggcgaaa
cccgacaggactataaagataccaggcgtttccccctggaagaccctcgtgcgctctcctgttccgaccctgccgctta
ccggatacctgtccgcctttctcccttcgggaagcgtggcgctttctcatagctcacgctgtaggtatctcagttcggtgta
ggtcgttcgctccaagctgggctgtgtgcacgaaccccccgttcagcccgaccgctgcgccttatccggtaactatcgt
cttgagtccaacccggtaagacacgacttatcgccactggcagcagccactggtaacaggattagcagagcgaggt
atgtaggcggtgctacagagttcttgaagtggtggcctaactacggctacactagaagaacagtatttggtatctgcgct
ctgctgaagccagttaccttcggaaaaagagttggtagctcttgatccggcaaacaaaccaccgctggtagcggtttttt
tgtttgcaagcagcagattacgcgcagaaaaaaaggatctcaagaagatcctttgatcttttctacggggtctgacgctc
agtggaacgaaaactcacgttaagggattttggtcatgagattatcaaaaaggatcttcacctagatccttttaaattaaa
aatgaagttttaaatcaatctaaagtatatatgagtaaacttggtctgacagttaccaatgcttaatcagtgaggcacctat
ctcagcgatctgtctatttcgttcatccatagttgcctgactccccgtcgtgtagataactacgatacgggagggcttacca
tctggccccagtgctgcaatgataccgcgagacccacgctcaccggctccagatttatcagcaataaaccagccagc
cggaagggccgagcgcagaagtggtcctgcaactttatccgcctccatccagtctattaattgttgccgggaagctaga
gtaagtagttcgccagttaatagtttgcgcaacgttgttgccattgctacaggcatcgtggtgtcacgctcgtcgtttggtat
ggcttcattcagctccggttcccaacgatcaaggcgagttacatgatcccccatgttgtgcaaaaaagcggttagctcct
tcggtcctccgatcgttgtcagaagtaagttggccgcagtgttatcactcatggttatggcagcactgcataattctcttact
gtcatgccatccgtaagatgcttttctgtgactggtgagtactcaaccaagtcattctgagaatagtgtatgcggcgaccg
agttgctcttgcccggcgtcaatacgggataataccgcgccacatagcagaactttaaaagtgctcatcattggaaaa
cgttcttcggggcgaaaactctcaaggatcttaccgctgttgagatccagttcgatgtaacccactcgtgcacccaactg
atcttcagcatcttttactttcaccagcgtttctgggtgagcaaaaacaggaaggcaaaatgccgcaaaaaagggaat
aagggcgacacggaaatgttgaatactcatactcttcctttttcaatattattgaagcatttatcagggttattgtctcatgag
cggatacatatttgaatgtatttagaaaaataaacaaataggggttccgcgcacatttccccgaaaagtgccacctgac
gtc//

Claims

1. A method for producing recombinant human thrombin from recombinant prothrombin using recombinant ecarin having the sequence SEQ ID NO 2 or a homologue thereof.

2. A method according to claim 1, wherein the recombinant ecarin is being expressed and secreted by a cell containing the gene comprising the nucleotide sequence SEQ ID NO 2 or a homologue thereof in CHO-S cells, which ecarin has an amino acid sequence equal to that of wild type ecarin.

3. A method according to claim 1 or 2, wherein recombinant protrombin is subjected to recombinant ecarin, which recombinant ecarin was isolated in active form after extra-cellular expression by CHO-S cells, said cells being left to apoptosis/necrosis for a time sufficient to activate said ecarin, whereupon a human recombinant thrombin is isolated.

4. A method according to any of the preceding claims, wherein the recombinant prothrombin is produced by a cell-line comprising a prothrombin expressing gene having a nucleotide sequence comprising the sequence SEQ. ID. NO. 1.

5. A method according to any of the preceding claims, wherein the recombinant prothrombin is a mixture of fully carboxylated prothrombin and incompletely carboxylated prothrombin.

6. A method according to any of the preceding claims, wherein the recombinant prothrombin is a fully carboxylated prothrombin.

7. A method according to any of the preceding claims, wherein the recombinant prothrombin is an incompletely carboxylated prothrombin.

8. A recombinant thrombin obtained by the method according to any of the preceding claims.

9. A pharmaceutical composition comprising a recombinant thrombin according to claim 8, in combination with pharmaceutically acceptable carriers, vehicles and/or adjuvants.

10. A pharmaceutical composition according to claim 9, wherein the composition is in an applicable form.

11. An isolated DNA sequence encoding ecarin according to SEQ ID NO 2 or a homologue thereof, having at least 80% identity to SEQ ID NO 2.

12. An isolated DNA according claim 11, wherein the homologue has an identity of at least 90% to SEQ ID NO 2.

13. A vector comprising the isolated DNA sequence of any of the claims 11 to 12.

14. An amino acid sequence encoded by SEQ ID NO 2 or a homologue thereof.

15. A host cell comprising the vector of claim 13.

16. A host cell according to claim 15, wherein the host cell is a mammalian cell.