Patent Application
20080153132
The present invention relates to a novel polypeptide. More specifically, the present invention relates to a genetic recombinant ecarin that specifically activates prothrombin and a process for preparing said genetic recombinant ecarin.
Some animals have a potent venom such as a snake venom, a spider venom, a scorpion venom, and a bee venom. It has been revealed that the venom comprises practically useful substance including a neurotoxin, a bleeding toxin, a thrombotic toxin, a physiologically active peptide, a cell growth factor activity, and the like.
Ecarin is a snake venom-derived protease isolated from Echis carinatus (T. Morita et al.: J. Biochem. 83, 559-570, 1978), known to specifically activate prothrombin. A cDNA encoding ecarin has been cloned by S. Nishida et al. (Biochemistry, 34, 1771-1778, 1995) to reveal its structure. Ecarin, a sugar protein, is a metalloprotease, a mature form of which has 426 amino acid residues in total, having a mosaic structure comprising a Zn2+ chelate, a disintegrin domain and a Cys-rich domain, with 61% homology to an H chain of RVV-X (Russell's viper venom X activator). Ecarin is quite a distinct enzyme from Factor Xa since its enzymatic activity is inactivated by EDTA but is not inhibited by DFP or antithrombin III.
Prothrombin, a target substrate to be activated by ecarin, is a precursor of thrombin, one of various blood coagulation factors. Thrombin, produced as a consequence of activation, is a multifunctional serine protease capable of interacting with various substrates and acting in a coagulation-anticoagulation manner within the living body. In human blood, prothrombin is activated by Factor Xa through restricted cleavage at two sites of prothrombin, i.e. Arg-Thr and Arg-Ile, whereas ecarin hydrolyzes prothrombin at the Arg-Ile alone to produce meizothrombin having a comparatively large molecular weight. Conversion of prethrombin-2 (product after removal of gla domain and Kringle domain from prothrombin) into active thrombin (α-thrombin) through Arg-Ile cleavage can surely be performed by ecarin based on its high substrate specificity. Although the Arg-Ile cleavage can also be done by trypsin, belonging to the same serine protease as ecarin, trypsin apt to cleave additional sites other than said cleavage site whereas ecarin never cleaves any other sites than said cleave site due to its high specificity as to the cleavage site. When trypsin is used to activate prethrombin-2, although partial activation of prethrombin-2 into α-thrombin is observed, most of the resulting α-thrombin is further degraded and hence complete conversion from prethrombin-2 into α-thrombin is not possible. On the contrary, when ecarin is added to prethrombin-2, conversion of prethrombin-2 into α-thrombin can quantitatively be done without any side products since ecarin only cleaves the unique Arg-Ile in prothrombin-2.
In the living process where prothrombin is converted into α-thrombin, prothrombin is activated via the intermediate called meizothrombin as described above. Within the living body, prothrombin is cleaved first at its Arg-Ile site by Factor Xa to produce meizothrombin, which is then cleaved by Factor Xa at the Arg-Thr site to complete activation to α-thrombin. Meizothrombin is known, though having a protease activity, to have a distinct substrate specificity from α-thrombin, as possessing an extremely low coagulating activity to fibrinogen while retaining an ability to activate protein C. Exhibiting such a characteristic substrate specificity, meizothrombin is readily converted into α-thrombin and hence does not stably exist within the living body since Factor Xa cleaves the two sites in prothrombin, i.e. Arg-Thr and Arg-Ile, as described above. Using ecarin for activation of prothrombin, however, meizothrombin can stably be prepared as ecarin cleaves the Arg-Ile site alone. Moreover, since ecarin also acts on abnormal prothrombin produced biosynthetically in the absence of Vitamin K, it is utilized for measuring blood level of such abnormal prothrombin.
As explained above, ecarin was found to possess an industrially useful activity. Up till the present, however, the only source is Echis carinatus and thus ecarin has not yet been industrially utilized due to its limited quantitative availability. Under the present circumstances, ecarin is sold as a reagent by reagent manufacturers but, due to high price as well as insufficient provision, it is not possible to use ecarin for activating prethrombin-2 or for preparing meizothrombin on an industrially applicable large scale. Besides, there is no guarantee that wild Echis carinatus is stably provided as a source and safety of working staffs must also be taken care of in view of the snake venom who handle a breeding of the snake. Putting all these accounts together, one may readily find that obtaining a large amount of ecarin is much difficult. Taking into a consideration a risk and limitation in preparing ecarin from Echis carinatus, another source and method allowing for provision of ecarin in a safer and more stable manner is desired.
Under the circumstances, a problem to be solved by the present invention is, aiming to establish a process for efficiently preparing thrombin on an industrial scale, to provide ecarin by the genetic recombination technique as a means for thrombin production.
The present inventors have earnestly investigated to solve the above-mentioned problems and as a result have completed the present invention that provides a process for efficiently preparing ecarin using the genetic recombination technique.
Thus, an object of the present invention is to provide a genetic recombinant ecarin (hereinafter also referred to as “recombinant ecarin”) capable of serving conversion from prethrombin-2 into α-thrombin or from prothrombin into meizothrombin via cleavage at the Arg-Ile site. This is attained by providing a protein with a molecular weight of about 80,000 having an amino acid sequence as set forth in SEQ ID NO: 1, or a peptide fragment or a series of peptide fragments having said amino acid sequence with one or several amino acid residues therein being deleted, substituted or added, or a partial sequence of either of the above amino acid sequences, or an amino acid sequence comprising as a part any of the above amino acid sequences.
Also provided by the present invention are a gene fragment that encodes the recombinant ecarin as described above and has a nucleotide sequence as set forth in SEQ ID NO: 2, or gene fragments that encode peptides having a partial amino acid sequence of said protein, as well as a plasmid comprising these gene fragments. The present invention also encompasses a recombinant microorganism and animal cell transformed with said plasmid. The present invention further encompasses a method for preparing a recombinant ecarin of interest or peptides having a partial amino acid sequence of the recombinant ecarin using these transformed microorganism or animal cells.
A gene encoding ecarin protein can be obtained by PCR using the sequence reported in the literature (S. Nishida et al., Biochemistry, 34, p. 1771-1778, 1995) as a template and synthetic DNAs as set forth in SEQ ID NO: 3 and SEQ ID NO: 4 as a primer pair.
Ecarin or a partial protein thereof can be prepared by incorporating a cDNA fragment encoding a portion of a structural region of a full length ecarin protein into an expression vector, transforming suitable microorganism or animal cells with the resulting expression vector, and culturing the transformant microorganism or animal cells to produce ecarin or a partial protein thereof. For production of a partial protein of ecarin, a peptide synthesizer may also be used.
An appropriate signal sequence for secretion in microorganism or animal cells may be linked to the upstream of a DNA encoding the protein of the present invention so that said protein may be expressed and secreted into a culture medium. The thus modified DNA for the purpose of secretion is advantageous in that the protein secreted into a culture medium can readily be recovered. Such a signal sequence includes pel B signal (S. P Lei et al., J. Bacteriology Vol. 169, 4379-4383, 1987) for E. coli; α factor signal (A. J. Brake, Yeast Genetic Engineering, p 269 Butterworth, 1989) for yeast; immunoglobulin signal SG-1 (H. Maeda et al., Hum. Antibod. Hybridomas Vol. 2, 124-134, 1991), C25 signal (Patent, International Publication No. WO94/20632) for animal cells, and the like.
An expression vector that can be used includes a plasmid, a viral vector, and the like. A promoter to be contained in the expression vector may be any promoter as far as it can ultimately provide active ecarin protein when combined with microorganism or animal cells as a host cell, including SV40 early promoter, SV40 late promoter, Cytomegalovirus promoter, chicken β-actin promoter, and the like. A marker gene includes, in case of an expression vector for a microorganism, an ampicilin resistance gene, tetracycline resistance gene for E. coli as a host; Leu2 gene for yeast as a host, and the like. In case of an expression vector for an animal cell, aminoglycoside 3′phosphotransferase (neo) gene, dihydrofolate reductase (dhfr) gene, glutamine synthetase (GS) gene, and the like, may be used.
In case of an expression vector for an animal cell, a variety of cells such as Chinese hamster ovary (CHO) cell, mouse myeloma cell, e.g. SP2/0, BHK21 cell, 293 cell and COS cell may be used as a host cell. With the thus constructed ecarin expressing cells, ecarin may be expressed transiently using e.g. COS7 cell (derived from African green monkey) or expressed stably using SP2/0 cell or CHO cell as a host cell.
A host cell may be transformed by any known methods including, for example, a calcium phosphate method, a DEAE dextran method, precipitation with e.g. lipofectin, fusion of protoplast with polyethylene glycol, electroporation, and the like. A method for transformation may suitably be selected depending on a host cell as used.
The recombinant ecarin of the present invention may be prepared as described below. The animal cells that stably express ecarin are cultured under normal conditions, for example, in MEM alpha culture medium containing 400 μg/mL to 1 mg/mL neomycin and 10% FCS in case that neomycin resistance gene is used as a marker gene to prepare neomycin resistant cells and then the enzymatic activity of ecarin in culture supernatant is measured. A clone that can grow under serum free conditions is then obtained from the ecarin producing transformants and cultured in a large scale. Ecarin is prepared and purified from the culture supernatant recovered therefrom with an index of the activity of ecarin to convert prothrombin into α-thrombin.
The recombinant ecarin of the present invention may be isolated and purified by any method conventionally used in the field of protein chemistry, as appropriately selected, including e.g. a salting out, ultrafiltration, isoelectric focusing, electrophoresis, ion exchange chromatography, hydrophobic chromatography, gel filtration chromatography, reverse phase chromatography, affinity chromatography, etc., with an index of the ability to activate prothrombin as described above. A preferable embodiment for purifying the recombinant ecarin includes a cation exchange chromatography and a gel filtration chromatography in this order under conditions as described in Example 9. This step allows for purification of the recombinant ecarin protein to around 2,600-fold higher specific activity with an activity yield of 13% with an index of the ability to activate prothrombin.
The fraction thus obtained after purification is then subject to sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) analysis in the presence of 2-mercaptoethanol to detect a main band of around 80,000 M.W. (
The thus obtained ecarin has an activity to activate prothrombin. The ecarin protein of the present invention may be utilized for preparing meizothrombin from prothrombin, for activating prethrombin-2 into α-thrombin, or for use as a detection reagent for abnormal prothrombin.
Besides, the ecarin protein or a polypeptide having a partial amino acid sequence thereof may also be utilized as an immunogen for preparing a polyclonal or monoclonal antibody by a conventional method. The thus prepared antibody capable of binding to the ecarin protein or a polypeptide having a partial amino acid sequence thereof as well as said protein or the polypeptide may be used in a detection system for an antigen such as Western blot or ELISA and as a material for constructing a diagnostic agent. Alternatively, the antibody may be bound to a suitable carrier for use in affinity chromatography to purify the antigenic proteins.
The present invention is explained in more detail by means of the following Examples which are not intended to restrict a scope of the present invention in any sense. Reagents used in the following Preparation and Examples were obtained from Pharmacia, BioRad, Wako Pure Chemical Industries, Ltd., TAKARA SHUZO CO., Ltd., Toyobo, and New England BioLabs.
(1) Construction of Expression Plasmid pCAGG-S1(Sal)
A chicken β-actin promoter-based expression plasmid pCAGG (Japanese Patent Publication No. 168087/1991) was digested with restriction enzyme EcoRI, blunt ended with T4 DNA polymerase, and then ligated with T4 DNA ligase in the presence of phosphorylated XhoI linker to construct pCAGG(Xho). The obtained pCAGG(Xho) was digested with restriction enzyme SalI, blunt ended with T4 DNA polymerase, and then ligated with T4 DNA ligase to construct pCAGG-Pv2. The resulting pCAGG-Pv2 was digested with restriction enzyme XhoI and then treated with S1 nuclease to erase several nucleotides in the vicinity of the XhoI recognition site. After the nuclease treatment, a single chain region was modified with T4 DNA polymerase in the presence of dNTPs and then ligated with T4 DNA ligase in the presence of phosphorylated SalI linker to construct pCAGG-S1(Sal).
(2) Construction of Expression Plasmid pCAGG-S1(Sal).dhfr
Expression plasmid pSV2-dhfr bearing DHFR gene (S. Subramani et al., Mol. Cell. Biol., 1, p. 854-864, 1981) was digested with restriction enzyme BglII, blunt ended with T4 DNA polymerase, and ligated with T4 DNA ligase to construct pSV2-dhfr-Bgn. The resulting pSV2-dhfr-Bgn was then digested with restriction enzyme PvuII and ligated with T4 DNA ligase in the presence of phosphorylated BglII linker to construct pSV2-dhfr-BgB. The obtained pSV2-dhfr-BgB was digested with restriction enzymes BglII and BamHI and was then subject to agarose gel electrophoresis to obtain a fragment of about 1.7 kbp. The expression plasmid PCAGG-S1(Sal) obtained above was digested with restriction enzyme BamHI and then ligated to cyclize with the 1.7 kbp fragment to construct pCAGGS1(Sal).dhfr.
(3) Construction of Expression Plasmid pCAGG-S1(Sal).dhfr.neo
An aminoglycoside phosphotransferase (neor)-based expression plasmid pMClneo-polyA (K. R. Thomas et al., Cell, 51, p. 503-512, 1987) was digested with restriction enzyme XhoI and then ligated with T4 DNA ligase in the presence of phosphorylated BamHI linker to construct pMClneo-2B. The resulting pMC1neo-2B was digested with restriction enzyme BamHI and then subject to agarose gel electrophoresis to obtain a fragment of about 1.1 kbp. The expression plasmid pCAGG-S1(Sal).dhfr obtained above was digested with restriction enzyme BamHI and then ligated to cyclize with the fragment of about 1.1 kbp to construct PCAGG-S1(Sal).dhfr.neo (
Using the nucleotide sequence of ecarin cDNA reported in the literature (S. Nishida et al., Biochemistry, 34, p. 1771-1778, 1995) as a template, PCR was conducted using a synthetic DNA having the sequence:
and a synthetic DNA having the sequence:
as a primer pair to introduce the recognition sites of restriction enzyme XhoI at both termini. The obtained gene was digested with restriction enzyme XhoI and subcloned into pUC18 to construct pUC.EC. A nucleotide sequence of the ecarin cDNA region of the resulting plasmid was determined by the conventional method to thereby obtain ecarin cDNA that has an exactly identical nucleotide sequence from the initiation codon to the termination codon to the sequence reported in the literature (SEQ ID NO: 2).
The ecarin cDNA obtained herein encodes the polypeptide as set forth in SEQ ID NO: 1.
The ecarin cDNA obtained in Example 2 was incorporated into the expression vector pCAGG-S1(Sal).dhfr.neo obtained in Example 1. The plasmid pCAGG-S1(Sal).dhfr.neo was digested with restriction enzyme SalI and then dephosphorylated with bovine small intestine derived alkaline phosphatase. The plasmid pUC.EC obtained above was digested with restriction enzyme XhoI and then a fragment of about 1.8 kbp encoding ecarin cDNA was purified by agarose gel electrophoresis. Then, the dephosphorylated plasmid and the fragment encoding ecarin cDNA were ligated to cyclize with T4 DNA ligase to construct PCAGG-S1.EC.dhfr.neo.
The ecarin expression plasmid pCAGG-S1.EC.dhfr.neo described in Example 3 was used to transform CHO cells and SP2/0 Ag14 cells. CHO cells were transformed by a modified calcium phosphate method whereas SP2/0-Ag14 cells were transformed by electroporation.
The expression plasmid for use in transformation was previously linearized by digestion with restriction enzyme PvuI.
Using CHO cells, transformants were selected from transformation as described below.
On the day previous to transformation, the cells were plated in MEM alpha medium with nucleic acids supplemented with 10% fetal calf serum in 10 cm dish at a cellular density of 5×105 cells/dish. After culture at 37° C. overnight, the cells were transformed with 20 μg/mL of the linearized expression plasmid pCAGG-S1.EC.dhfr.neo. After culture in 3% CO2 incubator at 35° C. overnight, the cells were washed with Dulbecco PBS(-) and the culture medium was replaced with nucleic acid free MEM alpha medium containing 10% dialyzed FCS and 500 μg/mL Geneticin. For selection, culture was continued in 5% CO2 incubator at 37° C. while replacing the culture medium every 3 to 4 days and emerged transformants were pooled and assessed for their ability to produce ecarin.
The transformed cells were plated in nucleic acid free MEM alpha medium supplemented with 10% dialyzed FCS at a density of 2×105 cells/mL and cultured overnight. The next day, the culture medium was replaced with serum free YMM medium (nucleic acid free MEM alpha medium with enriched amino acids/vitamins containing insulin, transferrin, ethanolamine and sodium selenite). After culture in 5% CO2 incubator at 35° C. for about 14 days, an ecarin level in culture supernatant was measured. As a result, 10 U/mL of ecarin in the culture supernatant was detected.
Using SP2/0 cells, transformants were selected from transformation as described below.
SP2/0 cells were washed twice with cooled Dulbecco PBS(-) and 107 cells suspended in 0.8 mL of PBS(-) were placed in a cuvette for electroporation (electrode width 0.4 cm; manufactured by BIO-RAD). The linearized expression plasmid (40 μg) was added and mixed with pipette. One pulse was applied at 0.22 kv at 975 μF using Gene Pulser II (manufactured by BIO-RAD). After the cuvette was cooled on ice for 10 minutes, the cell suspension was diluted with MEM alpha medium with nucleic acids containing 10% fetal calf serum (FCS) to about 5,000 cells/50 μL, plated on five 96-well plates each at 50 μL/well, and cultured in 3% CO2 incubator at 35° C. overnight. The next day, 50 μL/well of nucleic acid free MEM alpha medium containing 10% dialyzed FCS was added and culture was further continued overnight. The next day, 100 μL/well of nucleic acid free MEM alpha medium containing 1 mg/mL Geneticin and 10% dialyzed FCS was added. After culture for 10 to 14 days, emerged transformants at each well were assessed for their ability to produce ecarin. The cells were plated with nucleic acid free MEM alpha medium containing 500 μg/mL Geneticin and 2% dialyzed FCS at a density of about 3×105 cells/mL. After culture for about 14 days, an ecarin level in culture supernatant was measured. As a result, each of the transformants was found to express 2 to 10 U/mL of ecarin. Among these transformants, each 200 μL/well of those producing a high level ecarin were plated on 96-well plate at a concentration of 0.5 cell/well with the same culture medium for cloning by limiting dilution. Each of the obtained clones was assessed for their ability to produce ecarin. Each clone was plated with nucleic acid free MEM alpha medium containing 2% dialyzed FCS at a density of 3×105 cells/mL. After culture in 5% CO2 incubator at 35° C. for about 14 days, an ecarin level in culture supernatant was measured. Among the obtained clones, clone #1H-8 expressed 15 U/mL ecarin in culture supernatant.
This clone #1H-8 was adapted to serum free medium using YMM medium. YMM medium with 2% dialyzed FCS was used for culture and growth of the cells was confirmed. Thereafter, culture was continued while the serum level to be added was gradually lowered to 0.5% and further to 0.1%. After the cells were confirmed to proliferate well, they were cultured with completely serum free YMM medium. Growth of the cells was confirmed and then their ability to produce ecarin was assessed by the method described above using YMM medium. The clone #1H-8 after adaptation to serum free culture possessed an ability to produce 20 U/mL ecarin.
The ecarin producing cells #1H-8, adapted to serum free culture as described in Example 4, were subject to suspension culture with a spinner flask. After expansion of the cells, 250 mL of the cells were cultured with YMM medium in a 250 mL spinner flask (manufactured by Techne) at a density of 2×105 cells/mL. The cells were expanded to a 1 L spinner flask at a density of more than 1×106 cells/mL. After growth of the cells was confirmed, the cells were further expanded to five 1 L spinner flasks. The cells were cultured for about 7 days and then an ecarin level in culture supernatant was measured to detect expression of about 18 U/mL ecarin.
An amino acid sequence encoded by the ecarin cDNA was analyzed for its hydrophilic and hydrophobic regions in accordance with Hopp and Wood (T. P. Hopp et al., Proc. Natl. Acad. Sci. Vol. 78, 3824-3828, 1981). As a high hydrophilicity region, a peptide having the amino acid sequence: Lys-Asn-Asp-Tyr-Ser-Tyr-Ala-Asp-Glu-Asn-Lys-Gly-Ile-Val-Glu-Pro-Gly-Thr-Lys-Cys as set forth in SEQ ID NO: 5 was synthesized with a peptide synthesizer (manufactured by Applied). This peptide (500 μg) was inoculated to rabbit intradermally in the presence of Freund complete adjuvant on Day 0 and in the presence of Freund incomplete adjuvant on Day 14 and Day 28 to prepare a polyclonal antibody against the ecarin peptide. Western blot was used to confirm whether the obtained antibody recognizes ecarin. Natural ecarin was subject to SDS-PAGE in the absence of 2-mercaptoethanol. After electrophoresis, the gel was immersed in a transfer buffer (10 mM N-cyclohexyl-3-aminopropanesulfonic acid, 10% methanol, pH 11) for 5 minutes and then overlayed on PVDF membrane (Immovilon: Millipore) previously immersed in 100% methanol and the transfer buffer in this order to perform transfer at 160 mA for 16 hours using TRANS-BLOTCELL (BIO-RAD). After masking with TBST (50 mM Tris-HCl, pH 8.0; 150 mM NaCl; 0.05% Tween 20, containing 5% skim milk), the membrane was incubated with the serum diluted by 500-fold with TBST from rabbit to which the synthetic peptide was administered at room temperature for 1 hour and then washed with TBST. Then, the membrane was reacted with anti-rabbit IGG-HRP labeled antibody (Bio-Rad) diluted by 2,000-fold at room temperature for 1 hour. After washing, the membrane was dyed with Konica Immunostaining HRP 1000 (Konica) kit. As a result, the serum obtained by immunization with the synthetic peptide proved to specifically react with ecarin.
Culture supernatant (2000 mL) from the ecarin producing SP2/0 cells was diluted with a twice amount of water, adjusted to pH 5.0 with 1M citric acid and filtered through 0.45 μm filter to be used as a sample. The sample was applied to Macro-Prep High S Support (20 mL: Bio-Rad Laboratories) column equilibrated with 20 mM citrate (pH 5.0) buffer at a flow rate of 4 mL/min. The column was washed with the same buffer (150 mL) and then eluted with a gradient of salt concentration ranging from 0 mM to 1000 mM NaCl/20 mM citric acid (pH 5.0; 210 mL) at a flow rate of 4 mL/min. A portion of fractions was used for Western blot with the anti-ecarin antibody obtained in Example 6 to identify fractions with eluted ecarin, which were pooled and dialyzed against 20 mM sodium hydrogen carbonate buffer (pH 9.0) containing 50 mM NaCl.
The dialyzed product obtained in the process of cation exchange chromatography (1) above was applied to sulfate Cellulofine (2 mL: SEIKAGAKU CORPORATION) column equilibrated with 20 mM sodium hydrogen carbonate buffer (pH 9.0) containing 50 mM NaCl at a flow rate of 0.5 mL/min. The column was washed with the buffer described above (14 mL) and then eluted with a gradient of salt concentration ranging from 50 mM to 600 mM NaCl/20 mM sodium hydrogen carbonate (pH 9.0; 20 mL) at a flow rate of 0.5 mL/min. A portion of fractions was used for Western blot with the anti-ecarin antibody obtained in Example 6 to identify and pool fractions with eluted ecarin.
The fractions containing the recombinant ecarin obtained in the process of chromatography (2) above were applied to gel filtration column HiLoad 16/60 (Pharmacia) equilibrated with 10 mM phosphate (pH 7.0) buffer containing 100 mM NaCl and fractionated at a flow rate of 0.5 mL/min. A marker for gel filtration (Bio Rad) was used as a molecular weight standard. Each of the fractions was measured for an ability to activate prothrombin to detect a peak activity in a fraction of about M.W. 80,000. The obtained fraction of purified ecarin was subject to SDS-PAGE in the presence of 2-mercaptoethanol with subsequent treatment with Coomassie Brilliant Blue. The obtained pattern is shown in
The above three-step purification gave the recombinant ecarin with 13% of final activity yield and 2,600-fold higher specific activity as compared to culture supernatant.
To prothrombin (20 mM Tris-HCl, 100 mM NaCl, pH 8.5; 1 mg/mL; 40 mL) was added benzamidine to a final concentration of 50 mM. The recombinant ecarin was added to the mixture to a final concentration of 2 U/mL. The reaction mixture was incubated at 37° C. for 16 hours and then determined for the enzymatic activity of thrombin in accordance with the method as described below. As a result, the activity to cleave S-2238 was detected in prothrombin when added with the recombinant ecarin as shown in
It is known that ecarin specifically cleaves the peptide bond in prothrombin at the Arg-Ile site to produce A chain and B chain from prothrombin. The N-terminal amino acid sequence of thrombin B chain obtained after activation in Example 8 was determined.
The sample was run on SDS-PAGE gel containing 15% polyacrylamide with 2-mercaptoethanol treatment. After electrophoresis, the gel was immersed in a transfer buffer (10 mM N-cyclohexyl-3-aminopropanesulfonic acid, 10% methanol, pH 11) for 5 minutes and then overlayed on PVDF membrane (Immovilon: Millipore) previously immersed in 100% methanol and the transfer buffer in this order to perform transfer at 160 mA for 16 hours using TRANS-BLOTCELL (BIO-RAD). The PVDF membrane after transfer was washed with water, dyed with 0.1% Amide Black (containing 40% methanol, 1% citric acid) for 1 minute and then decolorized with distilled water. A dyed band corresponding to the molecular weight of B chain was cut and the membrane fragment was analyzed with 477A Protein Sequencer (Applied Biosystems). A sequence of ten amino acid residues at the N-terminus was determined: Ile-Val-Glu-Gly-Ser-Asp-Ala-Glu-Ile-Gly. This sequence is identical to the N-terminal amino acid sequence of B chain of α-thrombin derived from human blood, demonstrating that the recombinant ecarin obtained according to the present invention specifically cleaves the peptide bond at the Arg-Ile site in prothrombin like snake venom derived ecarin.
Measurement of activity of thrombin and ecarin in Examples as described above was performed as follows:
An activity of thrombin was measured as described blow.
A sample (20 μL), 50 mM Tris-HCl, pH 8.5 plus 50 mM NaCl buffer (60 μL), and 0.1% PLURONIC F-68 (20 μL) were added to 2008 tube (Falcon) and incubated at 37° C. for 3 minutes. A purified α-thrombin derived from human plasma (purchased from Hematologic Technology: HCT-0020) was used as a standard with dilution to 5, 2.5, 1.25, 0.625, and 0.3125 μg/mL using the same buffer. To the reaction mixture was added 100 μL of TestTeam developing substrate S-2238 (1 mM: DAIICH PURE CHEMICALS CO., LTD.) while stirring. After reaction at 37° C. for 5 minutes, the reaction was quenched with 800 μL of 0.1 M citric acid. The reaction solution (200 μL) was transferred to a 96-well plate and OD 405/650 was measured.
An activity of ecarin was measured as described blow.
A sample (20 μL), and 50 mM Tris-HCl, pH 8.5 plus 50 mM NaCl plus 0.1% PLURONIC F-68 buffer (“Buffer 1”; 60 μL) were added to 2008 tube (Falcon). Thereto was added 0.01% trypsin (2 μL) and the mixture was stirred and incubated at 37° C. for 10 minutes. The sample was diluted with Buffer 1 as needed depending on its concentration. To the reaction solution was added 10 μL of prothrombin (0.4 mg/mL; purchased from Hematologic Technology) and the mixture was reacted at 37° C. for 5 minutes. Then, 10 mM EDTA (10 μL) and TestTeam developing substrate S-2238 (1 mM; 100 μL) were added to the reaction mixture while stirring. After reaction at 37° C. for 5 minutes, the reaction was quenched with 800 μL of 0.1 M citric acid. The reaction solution (200 μL) was transferred to a 96-well plate and OD 405/650 was measured. For quantification of an ecarin activity, ecarin derived from snake venom (commercially available from Sigma) was diluted to 25 mU/mL, 12.5, 6.25, and 3.125 mU/mL with Buffer 1. Each 20 μL of these standard solutions was used in place of the sample without addition of the trypsin solution and the steps described above following the addition of prothrombin were repeated.
In accordance with the present invention, the recombinant ecarin protein that specifically activates prothrombin is provided. The recombinant ecarin prepared by the present inventors as described herein is a novel protein not previously reported. Thus, technical problems for attaining practical usage of a recombinant ecarin protein, such as construction of an expression vector that expresses an active ecarin protein, preparation of cells stably expressing a recombinant ecarin, and purification of a recombinant ecarin, are solved by the present invention, thus allowing for preparation of said protein on industrial scale.
| Number | Date | Country | Kind |
|---|---|---|---|
| 2001-206918 | Jul 2001 | JP | national |
The present application is a continuation of application Ser. No. 10/482,925, filed Jan. 6, 2004, which is the national stage under 35 U.S.C. 371 of PCT/JP02/06770, filed Jul. 4, 2002, which claims priority from JP2001-206918, filed Jul. 6, 2001. The entire contents of prior applications are herein incorporated by reference.
| Number | Date | Country | |
|---|---|---|---|
| Parent | 10482925 | Jan 2004 | US |
| Child | 11950638 | US |
