Patent Application
20070238128
The present invention relates to a method for screening substances that promote oligomerization of receptor protein molecules. More specifically, it relates to a method for screening physiologically active substances, which uses the oligomerization of receptor protein molecules as an indicator.
Physiologically active substances, such as erythropoietin and growth hormone, contribute to transduction of differentiative and proliferative signals through their binding to specific receptors expressed on the target cell membrane. In 1990, Yoshimura et al. reported that an EPO receptor carrying a mutation of Arg to Cys at position 129 in its extracellular domain induces transduction of a proliferative signal even in the absence of EPO, suggesting that it is important for signal transduction to multimerize the extracellular domains of EPO receptors via disulfide linkages (Nature, 348: 647-649, 1990). Further, X-ray structure analysis of the growth hormone-growth hormone receptor binding indicated that two growth hormone receptors bind to one growth hormone molecule (Journal of Molecular Biology, 222(4):865-868, 1991). The receptor multimerization is thus more likely to contribute to the first step of the signal transduction pathway induced by physiologically active substances.
In 1996, an EPO receptor-binding peptide having a core structure of 14 amino acids YXCXXGPXTWXCXP (X may be any amino acid) was reported to possibly mimic EPO activity (Science, 273:458-463, 1996). Crystal structure analysis of this peptide and the EPO receptor complex indicated that peptide dimer promotes EPO receptor dimerization (Science, 273:464-471, 1996).
Furthermore, an antibody against an extracellular domain of the EPO receptor has been found to possibly mimic EPO activity. Monovalent (Fab) fragments of this antibody can bind to the EPO receptor, but not induce signal transduction, suggesting that EPO receptor dimerization by binding divalent antibody is required for its function (J. Biol. Chem., 271(40):24691-24697, 1996).
Such a signal transduction pathway triggered by receptor multimerization is observed not only in EPO and growth hormone, but also in other physiologically active substances including interferons and granulocyte colony-stimulating factor (G-CSF). With regard to thrombopoietin, a peptide has also been identified that may mimic thrombopoietin activity through receptor multimerization (Science, 276:1696-1699, 1997).
Cunningham et al. show a method for selecting agonists and antagonists by detecting ternary complex formation of growth hormone receptors and its ligands (Japanese Patent Application No. 5-500070). However, this method detects homoquenching of fluorescent probes using a spectrofluorometer, and hence is not suitable for large-scale screening of test substances.
The object of the present invention is to provide a screening method of substitutes for physiologically active substances, which uses receptor multimerization as an indicator.
We have established a screening system permitting a convenient determination of whether receptor protein molecules or peptide fragments thereof are oligomerized by contact with test substance or not, and have thereby completed the invention.
The present invention provides a method for screening substances that promote oligomerization of receptor protein molecules or peptide fragments thereof, which comprises determining whether the receptor protein molecules or peptide fragments thereof are oligomerized when contacted with test substances. The test substance may be contacted with the receptor protein molecules or peptide fragments thereof in a cell-free environment.
In the above method, it is possible to measure signals generated by the oligomerization of the receptor protein molecules or peptide fragments thereof to determine whether the receptor protein molecules or peptide fragments thereof are oligomerized. The signals may be selected from the group consisting of scintillation signals, chemiluminescence signals, fluorescence signals, absorption signals, ionizing radiation signals, nuclear magnetic resonance signals, and surface plasmon resonance signals. Such signals may be measured by SPA method, RIA method, surface plasmon resonance, nuclear magnetic resonance, enzyme-linked immunosorbent assay, gel filtration chromatography and the like. At least one of the receptor protein molecules or peptide fragments thereof may be labeled. The label may be selected from the group consisting of radioisotope, fluorophore, enzyme, biotin, avidin, scintillant, and combinations thereof. To determine the presence of oligomerized molecules or fragments using SPA method, for example, at least one of the receptor protein molecules or peptide fragments thereof may be labeled with radioisotope, while at least one of the others may be attached to the surface of beads containing scintillant. In this case, a test substance can be added to an aqueous solution comprising the radiolabeled receptors or peptide fragments thereof as well as the receptors or peptide fragments thereof attached to the surface of scintillant-containing beads, and then the generated scintillation signals can be measured to determine whether the receptors or peptide fragments thereof are oligomerized. Those skilled in the art may properly determine the mixing ratio of the scintillant-containing beads (SPA beads) to the receptors to be attached to the beads according to the manufacturer's instructions.
The oligomers of the receptor protein molecules or peptide fragments thereof may be formed in a solution or on a solid surface. To determine the presence of the oligomers using nuclear magnetic resonance or gel filtration chromatography, in general, the oligomers are preferably formed in a solution. To determine the presence of the oligomers using SPA method, RIA method, surface plasmon resonance or enzyme-linked immunosorbent assay, in general, the oligomers are preferably formed on a solid surface.
The receptor may be a cytokine receptor selected from the group consisting of hematopoietic factor receptor, lymphokine receptor, growth factor receptor, and differentiation inhibitory factor receptor. More specifically, it may be selected from the group consisting of erythropoietin (EPO) receptor, thrombopoietin (TPO) receptor, granulocyte colony-stimulating factor (G-CSF) receptor, macrophage colony-stimulating factor (M-CSF) receptor, granulocyte-macrophage colony-stimulating factor (GM-CSF) receptor, tumor necrosis factor (TNF) receptor, interleukin-1 (IL-1) receptor, interleukin-2 (IL-2) receptor, interleukin-3 (IL-3) receptor, interleukin-4 (IL-4) receptor, interleukin-5 (IL-5) receptor, interleukin-6 (IL-6) receptor, interleukin-7 (IL-7) receptor, interleukin-9 (IL-9) receptor, interleukin-10 (IL-10) receptor, interleukin-11 (IL-11) receptor, interleukin-12 (IL-12) receptor, interleukin-13 (IL-13) receptor, interleukin-15 (IL-15) receptor, interferon-α (IFN-α) receptor, interferon-β (IFN-β) receptor, interferon-γ (IFN-γ) receptor, growth hormone (GH) receptor, insulin receptor, stem cell factor (SCF) receptor, vascular endothelial growth factor (VEGF) receptor, epidermal growth factor (EGF) receptor, nerve growth factor (NGF) receptor, fibroblast growth factor (FGF) receptor, platelet-derived growth factor (PDGF) receptor, transforming growth factor-β (TGF-β) receptor, leukemia inhibitory factor (LIF) receptor, ciliary neurotrophic factor (CNTF) receptor, oncostatin M (OSM) receptor, and Notch-like receptor.
The receptor protein molecule may be a cytokine receptor subunit. For example, each of IL-3 receptor, IL-5 receptor and GM-CSF receptor consists of α- and β-subunits. These receptors are known to share a common β-subunit. Each of IL-6 receptor, LIF receptor and IL-11 receptor consists of an α-subunit and gp130 subunit. These receptors are known to share a common gp130 subunit. Each of CNTF receptor and OSM receptor is a trimer of α-subunit, LIF receptor α-subunit and gp130 subunit. Also, each of IL-2 receptor, IL-4 receptor, IL-7 receptor, IL-9 receptor and IL-15 receptor consists of α-, β- and γ-subunits. These receptors are known to share a common γ-subunit.
The peptide fragment of the receptor protein molecule preferably comprises at least a ligand-binding site of the receptor. The receptor protein molecule has a ligand-binding site on its extracellular region or soluble region.
The oligomer that can be formed from the receptor protein molecules or peptide fragments thereof may be any homooligomer or heterooligomer including a dimer, trimer and tetramer. For example, erythropoietin receptor, thrombopoietin receptor, G-CSF receptor, SCF receptor and EGF receptor are known to form homodimers; IL-6 receptor, LIF receptor and IL-11 receptor are known to form heterodimers; and IL-2 receptor, CNTF receptor and OSM receptor are known to form heterotrimers.
A substance to be screened may be a novel substitute for a known physiologically active substance. The known physiologically active substance includes erythropoietin, interferon, G-CSF, growth hormone, thrombopoietin, GM-CSF and M-CSF.
In one embodiment of the above method, substances can be screened that promote dimerization of erythropoietin receptor protein molecules or peptide fragments thereof by adding a test substance to an aqueous solution comprising 125I-labeled erythropoietin receptors or peptide fragments thereof as well as erythropoietin receptors or peptide fragments thereof attached to the surface of scintillant-containing yttrium silicate or polyvinyl toluene beads; and then measuring generated scintillation signals to determine whether the erythropoietin receptors or peptide fragments thereof are dimerized.
The present invention also provides the substance identified by the above screening method that promotes the oligomerization of the receptor protein molecules or peptide fragments thereof. This oligomerization-promoting substance may be used as a novel substitute for a known physiologically active substance. It may be a cytokine receptor agonist, particularly an erythropoietin receptor agonist. It may have the ability to stimulate erythrocyte production.
The present invention also provides a pharmaceutical composition comprising the substance identified by the above screening method that promotes the oligomerization of the receptor protein molecules or peptide fragments thereof. The pharmaceutical composition of the present invention may be used as, for example, a therapeutic agent for renal anemia. The pharmaceutical composition of the present invention may comprise a therapeutically effective amount of the above oligomerization-promoting substance, together with an appropriate diluent, preservative, solubilizing agent, emulsifying agent and/or carrier. As used herein, “therapeutically effective amount” refers to an amount that achieves a therapeutic effect under defined conditions and in a defined method of administration. The pharmaceutical composition of the present invention may be formulated in any dosage form including solution, powder, or overcoated form. It may be administered via various routes including parenteral, oral, transpulmonal or transnasal route. Those skilled in the art may properly determine a dosage regimen (e.g., administration route, dosage, administration period, administration interval) according to the properties of the above oligomerization-promoting substance as an active ingredient and its dosage form, as well as the age, disease condition and the like of a patient to be treated.
The present invention also provides a method for screening substances that inhibit the oligomerization of the receptor protein molecules or peptide fragments thereof, which comprises determining whether the oligomerization of the receptor protein molecules or peptide fragments thereof in the presence of an oligomerization-promoting substance is inhibited when contacted with a test substance. The oligomerization-promoting substance may have a physiological activity. The substance that inhibits the oligomerization of the receptor protein molecules or peptide fragments thereof may have the ability to inhibit the physiological activity of the oligomerization-promoting substance. For example, the oligomerization-promoting substance may be erythropoietin, and the receptor may be an erythropoietin receptor.
The present invention also provides the substance identified by the above screening method that inhibits the oligomerization of the receptor protein molecules or peptide fragments thereof. This oligomerization-inhibiting substance may be used as an inhibitor against a known physiologically active substance. It may be a cytokine receptor antagonist, particularly an erythropoietin receptor antagonist. It may inhibit the ability of erythropoietin to stimulate erythrocyte production.
The present invention also provides a pharmaceutical composition comprising the substance identified by the above screening method that inhibits the oligomerization of the receptor protein molecules or peptide fragments thereof. The pharmaceutical composition of the present invention may be used as, for example, a therapeutic agent for diseases resulting from an elevated EPO level. The pharmaceutical composition of the present invention may comprise a therapeutically effective amount of the above oligomerization-inhibiting substance, together with an appropriate diluent, preservative, solubilizing agent, emulsifying agent, and/or carrier. The pharmaceutical composition of the present invention may be formulated in any dosage form including solution, powder, or overcoated form. It may be administered via various routes including parenteral, oral, transpulmonal or transnasal route. Those skilled in the art may properly determine a dosage regimen (e.g., administration route, dosage, administration period, administration interval) according to the properties of the above oligomerization-inhibiting substance as an active ingredient and its dosage form, as well as the age, disease condition and the like of a patient to be treated.
The present invention further provides a test kit for screening substances that promote the oligomerization of the receptor protein molecules or peptide fragments thereof, which comprises the receptor protein molecules or peptide fragments thereof and a buffer. For example, the receptor protein molecule or peptide fragment thereof may be an erythropoietin receptor protein molecule or peptide fragment thereof, and the buffer may be phosphate buffered saline.
The present invention further provides a test kit for screening substances that inhibit the oligomerization of the receptor protein molecules or peptide fragments thereof, which comprises an oligomerization-promoting substance, the receptor protein molecules or peptide fragments thereof, and a buffer. For example, the oligomerization-promoting substance may be erythropoietin; the receptor protein molecule or peptide fragment thereof may be an erythropoietin receptor protein molecule or peptide fragment thereof; and the buffer may be phosphate buffered saline.
The present invention will be further described below.
We first prepare receptor protein molecules and peptide fragments thereof. The receptor protein molecule or peptide fragment thereof may be in the form of a membrane fraction containing the receptor protein molecules or peptide fragments thereof, preferably may be isolated and purified from cells, more preferably may be produced recombinantly. For example, the receptor protein molecule or peptide fragment thereof may be prepared as follows.
When a membrane fraction is used, cells expressing the receptor protein molecules of interest may be solubilized in a buffer solution containing a surfactant such as Triton X-100, and then chromatographed using an affinity column on which ligands or anti-receptor antibodies have been immobilized in order to purify the receptor protein molecules.
When the receptor protein molecule has an identified ligand-binding site, a peptide fragment corresponding to this site may be synthesized and used in the present invention.
To produce the receptor protein molecule or peptide fragment thereof recombinantly, cDNA encoding the full-length receptor protein molecule or its extracellular region containing a ligand-biding site may be cloned using PCR method and cDNA library, and then integrated into an appropriate expression vector to express the gene of interest in a host cell such as E. coli or CHO cell. For the purpose of simple purification, a gene encoding a tag, such as MBP, GST or FLAG, may be ligated upstream or downstream of the gene encoding the protein of interest.
To detect the oligomer of the receptor protein molecules or peptide fragments thereof by RIA method or enzyme-linked immunosorbent assay, the receptor protein molecules or peptide fragments thereof have been previously labeled.
Next, to determine whether the receptor protein molecules or peptide fragments thereof are oligomerized, the molecules or fragments may be contacted with a test substance as follows.
In one embodiment of the present invention, we can measure the binding between receptors by scintillation technique. The scintillation technique can detect photon emission resulting from collisions between radioactive rays from some receptors labeled with radioisotopes and emission substances (i.e., scintillant) attached to the other receptors in oligomer complex. The resulting photon emission may be measured as a voltage pulse by means of a photomultiplier or a photodiode. The preferred emission substance includes crystals or powder of NaI, CsI and ZnS, or crystals of anthracene and naphthalene. Alternatively, scintillation proximity assay (SPA) technique developed by Amersham International (Bothworth N, and Towers P., 1989, Nature, 341, 167-168) can be used for this purpose. The SPA technique converts radiation energy from a radioisotope into light through absorption by scintillant-containing yttrium silicate or polyvinyl toluene beads (SPA beads) when the radioisotope binds to or is in close proximity to SPA beads. For example, some receptors are attached to SPA beads, while the other receptors are radiolabeled. Next, a test substance may be added to a solution comprising the radiolabeled receptors as well as the SPA beads-attached receptors, so as to detect the light resulting from the receptor oligomerization mediated by the test substance. Avidin and biotin can be used to attach the receptors to SPA beads. The radioisotope to be used includes 3H, 14C, 32P, 45Ca and 125I. Alternatively, we can use a microtiter plate containing scintillant on its bottom surface in place of SPA beads. For example, unlabeled receptors are immobilized on the bottom surface of the plate, and radiolabeled receptors and test substance are added thereto.
Upon formation of the receptor oligomer mediated by the test substance, the radiolabeled receptors build up on the bottom surface of the plate and the scintillant contained in the bottom surface absorbs radiation energy from the radioisotope, thereby causing photon emission. Increased photon emission results in the detection of the receptor oligomerization. The method using SPA beads is convenient and suitable for large-scale screening of test substances for their activity because there is no need to separate unbound receptors from bound receptors before detection.
In another embodiment of the present invention, surface plasmon resonance sensor, called BIACORE (developed by and commercially available from Pharmacia Biotech) can be used to detect receptor oligomerization. BIACORE has a basic structure including a light source, a prism, a detector and a microchannel. Some receptors have been immobilized on a cassette-type sensor chip, and the other receptors are then injected onto the sensor chip. The injected receptors are supplied to the sensor chip at a constant rate of flow and then distributed over the immobilized receptors. Upon formation of the oligomer through binding of the immobilized receptors with the injected receptors, the injected receptors build up on the sensor chip, resulting in increased volume of proteins on the chip. This increased volume can be detected optically as a plasmon resonance signal. For example, a test substance may be injected simultaneously with the receptors to detect an increased intensity of plasmon resonance signal, allowing the detection of the test substance activity from an increased plasmon resonance signal induced by the presence of the test substance.
In a further embodiment of the present invention, a nuclear magnetic resonance (NMR) technique can be used to detect receptor oligomerization. The NMR technique uses a low-energy electromagnetic wave, and is preferred due to its high sensitivity to detect even small energy changes. For example, two types of receptors are dissolved in a solvent at around 1 mM, followed by the measurement of nuclear magnetic resonance signals. Subsequently, a test substance is added to the solution. Nuclear magnetic resonance signals can be measured again so as to detect the receptor oligomerization as a signal shift.
In a further embodiment of the present invention, enzyme-linked immunosorbent assay (ELIZA) can be used. For example, some receptors are immobilized on each well of a 96-well plate and then reacted, in an appropriate medium, with a test substance and the other receptors labeled with an enzyme such as horseradish peroxidase or alkaline phosphatase. After washing, a coloring reagent is added to the plate, and absorbance for each plate is measured. The receptor oligomerization can be detected by increased absorbance. Receptor oligomerization can also be detected using chemiluminescence by labeling the receptors with luciferase as an enzyme and developing the plate by a coloring reagent. Alternatively, radiolabeled or fluorescently labeled receptors can be used instead of the enzyme-labeled receptors to detect receptor oligomerization. In this case, the detection may be accomplished by the measurement of the remaining ionized radiation dose or the fluorescence intensity.
In another embodiment of the present invention, a gel filtration chromatography technique can be used. Two types of receptors and a test substance are reacted under appropriate conditions and then subjected to gel filtration chromatography. The receptor oligomerization can be detected by a shift of a retention time for peak absorbance.
A substance that inhibits the oligomerization of the receptor protein molecules or peptide fragments thereof may be screened as follows.
An oligomerization-inhibiting substance can be screened by detecting a change in the signal intensity in the presence of a test substance, together with a substance that promotes the oligomerization of the receptor protein molecules or peptide fragments thereof.
For example, the oligomerization-inhibiting substance can be detected by adding an oligomerization-promoting substance and a test substance to an aqueous solution comprising 125I-labeled erythropoietin receptors or peptide fragments thereof as well as erythropoietin receptors or peptide fragments thereof attached to the surface of scintillant-containing yttrium silicate or polyvinyl toluene beads; and then measuring generated scintillation signals.
In one embodiment of the test kit according to the present invention, elements composing the kit may be packaged in a container(s), such as vial(s) or tube(s), separately or in combination or as a single unit. The container(s) may further be packaged as a single unit in a holder with several compartments. In this test kit, both of the receptor protein molecules or peptide fragments thereof and the oligomerization-promoting substance may be in lyophilized form. These elements may be reconstituted with a buffer when the test kit is used for the screening test.
This specification includes part or all of the contents as disclosed in the specification and/or drawings of Japanese Patent Application No. 10-102325 which is a priority document of the present application.
The present invention will be further described in the following examples, which are provided for illustrative purposes only and are not intended to limit the scope of the invention.
1) Two pairs of PCR primers (i.e., 4 primers in total) were designed based on EPO receptor cDNA sequence. Namely, the following 5′-primer ERO-1 and 3′-primer ERO-2 were prepared for the first PCR amplification:
To improve the accuracy of cloning, the following 5′-primer ERI-1 and 3′-primer ERI-2, which are internally adjacent to ERO-1 and ERO-2, respectively, were prepared for the second PCR amplification:
The primers ERI-1 and ERI-2 include an EcoR I site and a Hind III site, respectively in order to simplify subsequent subcloning.
2) AS-E2 cell line highly expressing EPO receptors (about 1×108 cells) was used to extract total RNA (1.23 mg) according to a modified AGPC method with phenol treatment and chloroform treatment. Oligo dT-latex beads were used to purify poly(A)+RNA (7.8 μg) from the whole total RNA. After confining the mRNA purity by electrophoresis, 1 μg of poly(A)+RNA was subjected to reverse transcription reaction using an Amersham cDNA synthesis kit. Two microliters of the resulting reaction mixture (20 μl in total) was subjected to PCR using LA Taq (Takara LA PCR kit ver2). ERO-1 & ERO-2 and ERI-1 & ERI-2 were used as PCR primer pairs. The PCR reaction was carried out under the following conditions: 2 minutes at 94° C., (20 seconds at 98° C./90 seconds at 60° C./3 minutes at 72° C.)×30 cycles, and 10 minutes at 72° C. A portion of this RT-PCR reaction mixture was electrophoresed in order to confirm the amplified fragment size.
3) The first strand cDNA synthesized from AS-E2 cell mRNA was used as a template and subjected to six separate PCR reactions using LA Taq (Takara), as described above. ERI-1 and ERI-2 were used as primers in these PCR reactions. Each of amplified PCR fragments was subcloned into a pBluescript II SK(+). One clone was selected for each PCR fragment to prepare a plasmid. The resulting six clone plasmids and PCR fragments (direct sequencing) were analyzed.
4) cDNA insert was excised with BamH I and Hind III from a EPO-R cDNA plasmid carrying two base substitutions, and then inserted into a BamH I/Hind III site of pUC 119 vector. This plasmid was digested with BssH II and Bal I to obtain a fragment including the vector (fragment 1). Meanwhile, a region between a BssH II site and a Bal I site was excised from a normal clone without any mutation in this region (fragment 2), which clone had been selected out of the six EPO-R cDNA clones prepared in 3) above. Fragments 1 and 2 were ligated to each other. The resulting clones were analyzed by sequencing, so as to isolate a clone into which fragment 2 had been correctly inserted (pUC 119-EPOR-L2). cDNA insert was excised from pUC 119-EPOR-L2 using BamH I and Hind III, and inserted into a BamH I/Hind III site of pBLSII SK(+) vector, thereby obtaining a clone (pEPOR-L2/SK).
1) To construct a human soluble EPO receptor gene, PCR was carried out using pEPOR-SK as a template and the following primers 1 and 2:
A reaction mixture (50 μl) containing 10 mM Tris-HCl (pH 8.3), 50 mM KCl, 1.5 mM MgCl2, 2.5 U Ex. Taq (Takara Shuzo Co., Ltd.), 0.25 mM dNTP, 0.2 μM primers 1 and 2, and 180 ng pEPOR-SK was overlaid with 15 μl Chill Out 14 (MJ Research Inc.). PCR amplification was carried out in a 480-model thermal cycler (Perkin-Elmer) for 30 cycles under the following conditions: 1 minute at 96° C., 1 minute at 60° C., and 2 minutes at 72° C., ending the amplification with an extra 10-minute holding at 72° C. The resulting PCR products was purified using a PCR purification kit (Qiagen), precipitated in ethanol, and dissolved in 8 μl TE. After addition of 1 μl 10× Buffer H (Takara Shuzo Co., Ltd.), the purified PCR products were digested with EcoR I and BamH I (0.5 μl, 10 U each) at 37° C. for 2 hours. The digested products were electrophoresed on 1% agarose gel to cut out a band of approximately 700 bp. This band was extracted and purified using a gel extraction kit (Qiagen), precipitated in ethanol, and dissolved in 5 μl TE. Similarly, 1 μg pUC 19 (Takara Shuzo Co., Ltd.) was digested with EcoR I and BamH I, precipitated in ethanol, and dissolved in 10 μl TE. The band (2 μl) and pUC 19 (1 μl) thus obtained were mixed and reacted with 1 μl T4 DNA ligase (Life Technologies Oriental Inc.) in 4 μl distilled water and 2 μl 5×T4 DNA ligase Buffer at 16° C. for 2 hours. The reaction mixture was then transformed into E. coli strain JM109 competent cells (Takara Shuzo Co., Ltd.) which had been melted on ice, and incubated for 30 minutes on ice. After additional incubation for 1 minute at 42° C. and then for 2.5 minutes on ice, the cells were further maintained at 37° C. in 500 μl SOC medium (Life Technologies Oriental Inc.) added thereto. The transformed cells (200 μl) were inoculated onto LBA-Amp plates and grown overnight at 37° C. Six colonies were picked out of the resulting colonies, each of which was then inoculated into 3 ml LB-Amp medium and streaked on an LBA-Amp plate, followed by culturing at 37° C. Subsequently, cells grown in each cell culture were suspended in distilled water and subjected to colony PCR under the conditions described above. The resulting PCR products were analyzed by agarose gel electrophoresis, confirming that each clone carries the inserted EPO receptor gene. E. coli cells were collected by centrifugation at 2,000 rpm for 15 minutes (Hitachi 05PR22) from each LB-Amp cell culture. A QIAprep-spin plasmid kit (Qiagen) was used to collect the plasmids in 100 μl TE. Each plasmid solution was analyzed by cycle sequencing in an ABI373A-model DNA sequencer (Perkin-Elmer) using a cycle sequencing kit (Perkin-Elmer), primers 1, 2, 3 and 4 and primer M13(−21) (Perkin-Elmer) or M13RV (Takara Shuzo Co., Ltd.). The plasmid solution prepared from a clone having the target sequence encoding the soluble EPO receptor was digested with EcoR I and BamH I under the conditions described above, followed by extraction and purification. The digested plasmid was ligated to pCHO1 which had been similarly digested and purified, and then transformed into E. coli strain JM109 competent cells under the conditions described above. Similarly, a plasmid solution was prepared and digested with EcoR I and BamH I, and then analyzed by agarose gel electrophoresis, thereby obtaining an expression plasmid pCHO/EpoR2 for the human soluble EPO receptor that carries the inserted target soluble EPO receptor gene.
2) Next, a CHO cell line expressing the human soluble EPO receptors was prepared.
A solution of pCHO/EpoR2 plasmid (30 μl) was mixed with 4 μl 10× Buffer K (Takara Shuzo Co., Ltd.), 4 μl 1% BSA solution and 2 μl Pvu I and incubated overnight at 37° C. After addition of 50 μl TE and 100 μl TE-saturated phenol, the solution was centrifuged at 14,000 rpm for 1 minute (MRX-150, Tomy Seiko Co., Ltd.) to recover an aqueous phase. This aqueous phase was mixed with 100 μl chloroform added thereto, and centrifuged at 14,000 rpm for 1 minute (MRX-150, Tomy Seiko Co., Ltd.) to recover an aqueous phase, followed by precipitation in ethanol. The precipitated products were dissolved in 20 μl sterile TE in order to measure its absorbance at 260 nm for calculation of its concentration. Ten microliters of Lipofect AMINE (Life Technologies Oriental Inc.) and 3 μg of Pvu I-digested plasmid solution were suspended in 0.3 ml α-MEM medium, followed by incubation at room temperature for 30 minutes. After washing with α-MEM, CHO cells grown to 70% confluency in 25T flask (Becton Dickinson & Co.) were cultured in 2.4 ml α-MEM in the presence of the Lipofect AMINE-plasmid mixture at 37° C. under 5% CO2 for 8 hours. The supernatant was discarded and the cells were maintained overnight in 5 ml α-MEM supplemented with 10% fetal calf serum (FCS). The supernatant was discarded again, and a cell culture was started in 5 ml α-MEM supplemented with 10% FCS (nucleic acid free, selective medium). The selective medium was changed every 2-4 days. After subculturing once in 75T flask, the cells were subjected to limiting dilution in five 96-½ well plates (Corning) such that the cells were diluted to 0.1 cells per well. Two weeks later, each well was observed by an inverted microscope to confirm proliferation of 89 clones. After washing with Dulbecco's PBS, the cells were collected by treating with a trypsin-EDTA solution. The collected cells were further grown in 24-well plates to confluency. The cell culture was continued for 4 days after changing the medium to obtain the culture supernatant. The soluble EPO receptors were detected by Western blot method using anti-FLAB M2 antibodies as primary antibodies, thereby obtaining a clone c165 expressing the soluble EPO receptors. The clone c165 was cultured in a selective medium containing 20 nM MTX, followed by limiting dilution, thereby obtaining 36 clones. The soluble EPO receptors in the culture supernatant were detected by Western blot method using anti-FLAG M2 antibodies or anti-EPO receptor antibodies (R&D systems) as primary antibodies, thereby obtaining a CHO cell line EpoR/CHO c165-19 expressing the soluble EPO receptors.
The culture supernatant of sEpoR-expressing CHO cells was filtered (pore size: 5 μm, Fuji Photo Film Co., Ltd.), and then passed through SARTOPURE PP filter (Sartorius) and SARTOBRAN P filter (pore size: 0.45+0.2 μm, Sartorius) to remove cell debris.
Bis-Tris HCl buffer was added to the resulting filtrate to 20 mM, which buffer had been prepared by dissolving Bis-Tris in water and adjusting to pH 6.0 with HCl. This filtrate was then applied at a flow rate of 4-5 ml/min to a Q Sepharose Fast Flow column (bed volume: 500 ml) equilibrated with 20 mM Bis-Tris HCl buffer (pH 6.0). This column was washed with 20 mM Bis-Tris HCl buffer (pH 6.0) to remove non-adsorbed protein, followed by elution with 20 mM Bis-Tris HCl buffer (pH 6.0) containing 0.5 M NaCl at a flow rate of 5-6 ml/min. Tris-HCl buffer was added to the resulting fraction to 50 mM, which buffer had been prepared by dissolving Tris in water and adjusting to pH 7.3 with HCl. This fraction was then applied at a flow rate of 1 mL/min to an anti-FLAG M2 affinity column (bed volume: 10 ml, Eastman Kodak Co.) equilibrated with TBS solution (Takara Shuzo Co., Ltd.).
Proteins adsorbed to the anti-FLAG M2 affinity column were eluted with 0.1 M glycine HCl buffer (pH 3.5) and adjusted to neutral pH by adding about 1/10 volumes of 1 M Tris-HCl buffer (pH 8.0), followed by reversed-phase HPLC using a Vydac Protein C4 column (Vydac). That is, the proteins were adsorbed to a Vydac Protein C4 column equilibrated with a 0.1% trifluoroacetic acid solution containing 20% acetonitrile, and then eluted with a linear acetonitrile gradient up to 80% over 60 minutes. The elution using this HPLC technique resulted in a single elution peak, thereby obtaining purified sEpoR.
The purified sEpoR from Example 3 was subjected to solvent replacement with 0.1 M sodium bicarbonate buffer (pH 8.6). Namely, sEpoR was dissolved in 0.1 M sodium bicarbonate buffer (pH 8.6) after drying in a centrifugal concentrator under reduced pressure, or was applied to a Fast Desalting column (Pharmacia) equilibrated with 0.1 M sodium bicarbonate buffer (pH 8.6).
A biotinylating reagent (Amersham) was added to the proteins to be labeled in an amount of 40 μl per mg protein, and reacted at room temperature for one hour while stirring. The reaction mixture was applied to a Bio-Gel P-6 column (Bio-Rad Laboratories) equilibrated with PBS solution containing 0.02% Tween 20 to remove unreacted reagents, thereby obtaining a protein fraction containing biotinylated sEpoR.
The purified sEpoR from Example 3 was subjected to solvent replacement with 0.1 M sodium bicarbonate buffer (pH 8.6). Namely, sEpoR was dissolved in 0.1 M sodium bicarbonate buffer (pH 8.6) after drying in a centrifugal concentrator under reduced pressure, or was applied to a Fast Desalting column (Pharmacia) equilibrated with 0.1 M sodium bicarbonate buffer (pH 8.6).
A vial containing 125I-Bolton and Hunter reagent (Amersham) was exposed to a nitrogen gas stream to evaporate the solvent contained therein. Fifteen microliters of sEpoR solution (ca 1 mg/ml) was added to this vial and reacted with the reagent on ice for 30 minutes while stirring every 5 minutes. The reaction continued for additional 5 minutes on ice after addition of 500 μl 0.1 M sodium bicarbonate buffer (pH 8.6) containing 0.2 M glycine.
The reaction mixture was applied to a Sephadex G-25 column (Pharmacia) equilibrated with 0.1 M phosphate buffer (pH 7.2) containing 0.25% gelatin to remove unreacted reagents, thereby obtaining a protein fraction containing 125I-labeled sEpoR.
50 μg streptavidin-attached SPA beads (Amersham), biotinylated sEpoR and about 150,000 cpm 125I-labeled sEpoR were dissolved in 100 μl test buffer (Dulbecco's PBS(−) containing 0.1% BSA and 5 mM EDTA) to prepare a test solution. Meanwhile, EPO receptor-binding peptide dimers were prepared by asking Peptide Institute, Inc. to synthesize them as described in Science, 273:458-463, 1996; Blood, 88(10):542a, 1996; Science, 276:1696-1699, 1997. The EPO receptor-binding peptide dimers were mixed and reacted with the test solution at room temperature for 12 hours, followed by detection using Microbeta (Pharmacia).
Structure of EPO receptor-binding peptide dimer
(wherein X represents β-Ala)
Signals whose intensity depends on the concentration of the EMP1 dimer were generated from the SPA beads, resulting in the detection of EPO receptor dimerization (
The present invention provides a method for screening substitutes for physiologically active substances, which uses receptor multimerization as an indicator.
All publications, patents and patent applications cited herein are incorporated herein by reference in their entirety.
| Number | Date | Country | Kind |
|---|---|---|---|
| 102325/1998 | Apr 1998 | JP | national |
| Number | Date | Country | |
|---|---|---|---|
| 20060183153 A1 | Aug 2006 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 09673084 | Oct 2000 | US |
| Child | 10903068 | Jul 2004 | US |
