WO1992015606A1 - Neue inhibitoren der endothelzell-proliferation - Google Patents
Neue inhibitoren der endothelzell-proliferation Download PDFInfo
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- WO1992015606A1 WO1992015606A1 PCT/EP1992/000419 EP9200419W WO9215606A1 WO 1992015606 A1 WO1992015606 A1 WO 1992015606A1 EP 9200419 W EP9200419 W EP 9200419W WO 9215606 A1 WO9215606 A1 WO 9215606A1
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/435—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans
- C07K14/46—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates
- C07K14/47—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals
- C07K14/4701—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from animals; from humans from vertebrates from mammals not used
- C07K14/4702—Regulators; Modulating activity
- C07K14/4703—Inhibitors; Suppressors
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
Definitions
- angiogenesis takes place in an orderly sequence of steps: at a point at which a new vascular process begins to grow (mostly in the area of post-capillary venules), endothelial cells locally break down the basement membrane and migrate in the direction the source of a factor stimulating angiogenesis, grow and divide, form a vascular lumen and meet other vascular rungs or existing capillaries, so that a new capillary section arises which finally surrounds itself with a newly formed basal membrane.
- angiogenesis is absolutely necessary for the growth of tumors with a diameter of over 1 to 2 mm.
- Avascular tumors are limited to a very small size due to the limited diffusion in the supply of gases and nutrients and in the removal of waste materials.
- the inability of solid tumors to grow to a clinically significant size or to form metastases in the absence of successful induction of angiogenesis has aroused great interest in the study of compounds which inhibit angiogenesis.
- E The commercial applicability of such inhibitors lies in the inhibition of tumor growth in general, in particular in the inhibition of tumors based on endothelial cells, such as Kaposi's sarcoma and hemangiomas.
- endothelial cells such as Kaposi's sarcoma and hemangiomas.
- other diseases which are based on excessive capillary growth.
- diabetic retinopathy and retrolental fibroplasia both eye diseases.
- Another application is in the treatment of wounds, where an angiogenesis inhibitor can be used to regulate wound healing, ie in delaying the formation of new blood vessels.
- an angiogenesis inhibitor in the treatment of rheumatoid arthritis. In this disease, vascularization of the cartilage is observed (as is generally the case with any inflammation in this area), which could be suppressed with an angiogenesis inhibitor.
- protamine (Taylor and Folk an, Nature 297 (1982), 307-312), angiostatic steroids (Cru et al., Science 230 (1985), 1375-1378), a placental RNAse inhibitor (Shapiro and Vallee , Proc. Natl. Acad. Sci. USA 84 (1987), 2238-2241) and a number of compounds which influence matrix synthesis and stability (see, for example, Ingber and Folkman, Lab. Invest. 59 (1988), 44-51 ). With some of these inhibitors, inhibition of tumor growth or regression in vivo was found, but not in all tumors. The toxicity of these angiogenesis inhibitors also remains a problem. By Rastinejad et al.
- an angiogenesis inhibitor was found in a medium with hamster cells and hamster-human hybrid cells, which suppresses neovascularization in vivo.
- This compound is apparently a glycoprotein with a molecular weight of 140 kDa.
- this inhibitor shows little stability, in particular it is not heat-stable.
- DE 40 06 609 discloses a protein which acts as an inhibitor of the proliferation of endothelial cells, obtainable from baby hamster kidney cells, which has a molecular weight of approx. 60 to 100 kDa under gel conditions under native conditions and greater heat stability shows.
- the object of the present invention was to provide further angiogenic inhibitors which can be used therapeutically as an alternative and supplement to inhibitors which are already known.
- the object of the invention is achieved by a method for enriching inhibitors of the proliferation of endothelial cells from the tissue of vertebrates, which is characterized in that
- tissue extract is placed on a cation exchanger and the substances binding to the cation exchanger are subjected to fractionation
- step (c) the active fractions from step (b) are separated by gel filtration chromatography, and
- step (d) the active fractions from step (c) are purified by HPLC reverse phase.
- tissue of vertebrates chosen as the starting material for the method according to the invention can be of embryonic as well as adult origin. It is preferred to use em-
- E bryonic tissue from birds or mammals particularly preferably tissue from chicken embryos as starting material. Furthermore, it is preferred to use adult brain tissue from birds or mammals, in particular adult bovine brain, as the starting material.
- adult brain tissue from birds or mammals, in particular adult bovine brain, as the starting material.
- the method according to the invention can also be applied to human tissue (both embryonic and adult origin).
- EMBIN I The inhibitor of the proliferation of endothelial cells, which is referred to as EMBIN I and which can be obtained by the process according to the invention, is distinguished by the fact that upon gel electrophoresis in the SDS polyacrylic gel it forms a band with an apparent molecular weight in the range from 2.5 to 6. 2 kDa results.
- EMBIN I shows an undiminished inhibition of endothelial cell proliferation. ration. EMBIN I thus proves to be a very heat-resistant compound if one assumes that very few proteins can survive such a treatment while maintaining their activity.
- EMBIN I is resistant to a number of different proteases.
- proteases were tested: trypsin, S. aureus V8 protease, clostripain, thermolysin, subtilisin, pronase E, proteinase K, carboxypeptidase Y, papain, pepsin (Sigma), chy otrypsin, pyroglutamate aminopeptidase, endoproteinase Arg-C , Endoproteinase Lys-C (Boehringer Mannheim), proline-specific endopeptidase (Seikagaku Kogyo, Japan).
- EMBIN I is present as a peptide associated with nucleic acid molecules, e.g. for the angiogenesis factor "angiotropin" (Wissler et al., Protides Bio.Fluids. 34 (1986), 525-536), EMBIN I was incubated with both DNAse and RNAse. No change in the migration behavior was found during the gel electrophoresis.
- EMBIN I could be a glycopeptide
- digestions with glycolytic enzymes were carried out.
- EMBIN I was subjected to a sequential digestion first with neuraminidase and then with ⁇ -galactosidase.
- EMBIN I was also treated with glycopeptidase F. It was also examined whether EMBIN I shows a reaction with the "Glycan Detection Kit" from Boehringer Mannheim. None of these experiments
- AMBIN I is a substance with protein character
- Diethylpyrucarbonate reacts with free ⁇ -amino groups or with the e-amino groups of lysine to form an N-carboxy derivative.
- EMBIN I was treated with diethyl pyrocarbonate, it was found that the inhibitory activity was completely eliminated. This suggests that the inhibitory activity of EMBIN I is based on one or more functionally important amino groups.
- the fact that the inhibitory activity of EMBIN I can also be abolished when treated with phenol is a further indication of the peptide character of this substance.
- EMBIN I can be stained with the ninhydrin spray reagent (which serves to detect amino groups).
- EMBIN I can be a peptide
- protein determination by the method of Lowry is possible .
- EMBIN I is a peptide
- the N-terminus of the molecule appears to be blocked because sequencing of EMBIN I according to the Edman method, for which a free ⁇ -amino group of the peptide is necessary, was necessary not yet possible.
- EMBIN I Another unusual property of EMBIN I is the difference in migration behavior during gel filtration on the one hand and SDS-PAGE on the other.
- the EMBIN I activity is eluted on a gel filtration column at a position which corresponds to a molecular weight of approximately 500 to 1000 Da.
- the band of EMBIN I is found in the range between approximately 2.5 and 6.5 kDa, regardless of the electrophoresis system used.
- the other inhibitor ANEMIN obtainable by the process according to the invention also shows this difference in the migration behavior during gel filtration and SDS-PAGE.
- ANEMIN a band in the range of 16 to 20 kDa is found in the SDS-PAGE, while after gel filtration the molecular weight should be less than 1000 Da.
- ANEMIN is very stable and resistant to proteases.
- Step (a) is the homogenization and centrifugation of the tissue selected as the starting material.
- Adult bovine brain or 4 to 10 day old chicken embryos are preferably used as the starting material.
- other types of tissue in particular embryonic tissue or brain tissue from other species, are also suitable.
- a tissue extract is obtained which can be fed to the further process stages.
- the steps of homogenization and centrifugation can be carried out by customary methods known to the person skilled in the art and are not particularly critical for the method according to the invention.
- Step (b) of the process according to the invention consists in placing the tissue extract on a cation exchanger and subjecting the substances which bind to the cation exchanger to a fractionation.
- the inhibitors according to the invention are able to bind to a cation exchanger at approximately neutral pH conditions and salt concentrations of up to 100 mmol / l, while a large part of the substances contained in the tissue extract are unable to do so.
- the elution of the substances according to the invention from the exchange column can e.g. by increasing the salt concentration to 700 mmol / 1.
- a CM-Sepharose matrix (Pharmacia / LKB) has proven to be a suitable cation exchanger. However, other cation exchangers can also be used.
- Fractions from the cation exchanger eluate which show an inhibition of the proliferation of endothelial cells in an in vitro activity test (infra), can be separated by gel chromatography according to step (c) of the method according to the invention.
- the active fractions are first passed through a hydroxylapatite column and then subjecting the passage through the hydroxylapatite column to ultrafiltration.
- chromatography on hydroxylapatite only a very small amount of protein is not bound by the hydroxylapatite matrix. Since the inhibitors according to the invention are in the passage of the column (ie they do not bind), a good cleaning effect is achieved by this step.
- Ultrafiltration was carried out in order to reduce the volume of the active protein fraction present after the hydroxylapatite roatography before the gel filtration step. Due to the low molecular weight of the inhibitors, the concentration is carried out over a 500 Da membrane. The inhibitory substances are then found in the retentate; the filtrate has no inhibitory effect on endothelial cell proliferation.
- Ultrafiltration can also be used for extensive desalination of the sample using two diafiltration steps.
- the volume of the sample is then about 1/6 to 1/10 of the initial volume.
- a further concentration can be achieved by subsequent lyophilization of the sample and absorption of the lyophilisate in a minimum volume of 0.2 M acetic acid.
- the gel filtration column to which the sample is subsequently applied can also be equilibrated with this buffer.
- Step (c) of the process according to the invention is a gel chromatographic separation of the active fractions obtained to date.
- Biogel P2 which has a nominal exclusion size of about 1.8 kDa, has proven to be a suitable material for gel filtration.
- the inhibitory substances are not eluted in the excluded volume of the column under the chosen conditions. Consequently, the inhibitory substances should have a molecular weight of less than 1800 Da.
- Step (d) of the method according to the invention for the enrichment of the inhibitory substances is a purification by reverse phase HPLC.
- Different matrix matrices from different manufacturers were used for the reverse phase HPLC and a trifluoroacetic acid / acetonitrile gradient as eluent.
- the inhihitorically effective substances could not be bound to the column in this procedure, but were regularly found in the proportion of unbound substances. From gel electrophoretic analysis of the individual fractions, it was evident that a broad band with a molecular weight in the range from 2.5 to 6.5 kDa (EMBIN I) was present in the inhibitory fraction.
- Organic sulfonic acids in particular alkyl or aryl sulfonic acids, are suitable as acidic ion pair formers.
- these sulfonic acid molecules can interact with the hydrophobic groups of the column matrix via their hydrophobic alkyl component, while at the same time they can bind positively charged substances via their sulfonic acid grouping.
- the concentration of the sulfonic acid is advantageously between 0.1 and 50 mmol / 1, particularly preferably between 1 and 10 mmol / 1.
- EMBIN I binds to an Asahipak ODP 50 column equilibrated with 5 mmol / 1 heptanesulfonic acid, pH 3.5 and can be eluted again in a linear gradient.
- the ANEMIN-containing fractions of the gel chromatography can also be analyzed by reverse phase HPLC, e.g. be further purified in the presence of heptanesulfonic acid as an ion pair former analogous to EMBIN I.
- heptanesulfonic acid as an ion pair former analogous to EMBIN I.
- electrophoresis in polyacrylamide gel the band for ANEMIN is found in the range between 16 and 20 kDa.
- the method according to the invention allows the inhibitors for the proliferation of endothelial cells, referred to as EMBIN I or ANEMIN, to be produced as pure substances, tissue from chicken embryos being used as the starting material. If adult bovine brain is used as the starting material, it is possible with identical process steps to obtain two corresponding substances, that of electrophoresis
- REPLACEMENT LEAF have the mobility properties of EMBIN I and ANEMIN in polyacrylamide gel.
- the activity of the inhibitory substances was analyzed in vitro by the BAEC test and in vivo by the CAM test, which are shown in detail in Example 1 below.
- the substances according to the invention can be used in the treatment of all diseases in which an increased angiogenesis takes place and which have already been mentioned above.
- the substances according to the invention for inhibiting tumor growth such as Kaposi sarcomas. or hemangiomas, for the treatment of eye diseases in which increased capillary growth occurs, in particular diabetic retinopathy and retrolental fibroplasia, and in rheumatoid arthritis or for regulating wound healing.
- the preferably used dose of the substances according to the invention per kg of body weight should be in the order of ⁇ g to a maximum of mg.
- Fig. 1 a gel filtration chromatography of the tissue extract from chicken embryos
- Fig. 2 the inhibition of endothelial cell proliferation of the fractions from gel chromatography
- Fig. 3 the protein pattern of fractions 11-17 from gel filtration
- Fig. 4 the elution profile of EMBIN I in RP-HPLC in TFA / acetonitrile
- Fig. 5 the elution profile of EMBIN I in RP-HPLC at pH 12.5
- Fig. 6 the elution profile of EMBIN I in the presence of
- Fig. 8 an SDS-PAGE from ANEMIN.
- Retina factor is an aqueous extract from bovine retinae which essentially contains bFGF as the endothelial cell mitogen (basic fibroblast growth factor; Mascarelle et al. 1987).
- the retinae from 25-50 cattle eyes were dissected out and incubated with the same volume of PBS (phosphate buffered saline) at 4 ° C until the next day (D'A ore et al., J.Cell.Biol. 99 (1984), 1545-1549). The preparation was gently stirred several times.
- the solid constituents were first removed by centrifugation at 1000 rpm (Heraeus) for ten minutes, the supernatant was then centrifuged again at 45,000 g for 30 minutes (Sorvall, SS34). The supernatant from the second centrifugation was aliquoted and frozen at -20 ° C. Before use, the aliquots were sterile filtered (0.2 or 0.45 ⁇ pore size).
- Endothelial cell cultures obtained from bovine aortas were used to demonstrate the inhibition of endothelial cell proliferation.
- BAEC bovine aortic endothelial cells
- FCS fetal calf serum
- the proliferation of the endothelial cells is strongly simulated by adding retina factor to the medium. After changing the medium, the samples to be tested were added (up to 40 ⁇ l / well). The cells were incubated for a further 3 days at 7.5% CO 2 and at 37 ° C., then (day 5) the cell number was determined in the Coulter Counter. This conception of the tests checked the samples examined for the content of substances which can inhibit the proliferation of endothelial cells, even in the presence of mitogens.
- the cells were washed with Ca and Mg-free PBS, trypsinized to remove them from the pad (0.5 ml 0.05% trypsin / 0.02% EDTA solution, Gibco) and in 9, 5 ml of isotonic solution transferred.
- the cell number was determined in a Coulter Counter, Industrial D (attenuation: 2; aperture gurrend: 0.0093; threshold: 12; capillary drilling: 200 ⁇ m).
- the graphical evaluation of the data obtained was carried out with the programs "Cricket Graph" and "Kaleidagraph" on computers from Apple.
- SMC smooth muscle cells
- NIH 3T3 fibroblasts NIH 3T3 fibroblasts
- the fractions to be tested were mixed with the same volume of a sterile 1% methyl cellulose solution (4000 cpi; Sigma) in a ratio of 1: 1.
- the methyl cellulose discs were pulled off the Teflon rods and carefully placed on the CAM on development day E6 or E7. After 48 or 72 hours, the areas of the CAM in the vicinity of the methyl cellulose discs under the binocular were examined for inhibition of angiogenesis.
- the embryos were injected into an allantoic vein by means of a glass capillary with about 20 ⁇ l of a solution of 40% Luconyl blue (Hoechst) in PBS.
- Hoechst Luconyl blue
- Hatching eggs from H ⁇ lzl (Wasserburg am Inn) were used as the starting material. 4-10 days after the eggs started incubating, they were opened over a large Petri dish and the embryos were removed. The amnion skin and, above all, the allantois were prepared as completely as possible from the embryos in order to eliminate influences from the allantois fluid, which represents the embryonic urine. The embryos were stored frozen at -20 ° C until extraction and thawed overnight at 4 ° C before preparation.
- 2500-3500 chicken embryos from development days E4 to E10 corresponding to a wet weight of 1.8 to 3 kg, were taken in 300 g portions with a total of 1.5 to 2 1 extraction buffer (20 M MOPS pH 6.8 / 100 M NaCl / 2 mM PMSF) homogenized in a kitchen mixer from Braun. The homogenate was then extracted for 30 min at 4 ° C. with stirring and the insoluble constituents were separated off by centrifugation at 22,000 g for 90 minutes (Sorvall, GSA rotor).
- CM-Sepharose Fast Flow The extract obtained in the first step was pumped onto a CM-Sepharose column (Pharmacia / LKB, Freiburg; 50 x 250 mm), which was coated with application buffer (20 mM MOPS pH 6.8 / 100 mM NaCl) had been equilibrated. The flow rate was 500 ml / h. After the extract had been applied, the column was washed with an application buffer until the absorption at 280 n had reached a minimum. 86% of the total protein was in the run. The proteins bound to the column, including the inhibitory substances EMBIN I and ANEMIN, were then eluted in one step with 700 mM NaCl in 20 mM MOPS pH 6.8.
- the gel bed for this was packed at a flow rate of 50 ml / h after the dry hydroxyapatite powder (Bio-Gel HTP, BioRad, Kunststoff) had swelled sufficiently in the application buffer (20 mM MOPS, pH 6.8).
- the eluate from the cation exchange chromatography was then applied directly in 2-3 portions at 40 ml / h to the hydroxylapatite column (25 x 100 mm) equilibrated in 20 mM MOPS pH 6.8, which was then used for as long as Equilibration buffer was washed until absorption at 280 nm was minimal. Only a very small proportion of protein (including the inhibitory substances) was not bound by the hydroxyapatite matrix and was in the passage of the column.
- the material reversibly bound to the hydroxylapatite matrix could be eluted with 0.4 M potassium phosphate buffer pH 6.8. This eluate was then dialyzed against 2 ⁇ 5 1 20 mM MOPS buffer pH 6.8 or against 0.5 ⁇ PBS pH 7.2. Visking dialysis tubes with a nominal separation limit of 10-15 kDa were generally used.
- the material not bound to hydroxyapatite was concentrated over a YC05 ultrafiltration membrane (Amicon GmbH, Witten, nominal exclusion limit: 500 Da) in an ultrafiltration cell (Amicon GmbH, Witten; type 8400) to about a tenth of the starting volume.
- the solution was desalted in the same chamber by diafiltration with dist. Water.
- the largely desalinated concentrate from the ultrafiltration was lyophilized to further reduce the solution volume.
- a Bio-Gel P2 column (BioRad, Kunststoff; 200-400 esh; nominal excl. Weight: 1800 Da) was used for the gel filtration of the lyophilisates taken up in approx. 4-6 ml of 0.2 M acetic acid 0.2 M acetic acid had been equilibrated.
- the sample was applied to the column using a peristaltic pump (LKB / Pharmacia) and the gel filtration was accomplished by pumping the eluent onto the column.
- the flow rate during the gel filtration was 6 ml / h, the detection of the separated proteins and peptides was carried out at 280 nm.
- Fig. 1 shows gel filtration chromatography on a Biogel P2 column. The major part of the applied proteins and peptides is eluted in the exclusion volume of the column (fractions 5-10). Fractions 17-20 contain the salt which is still present and at the same time mark the lower limit of exclusion of the column. The fractions of the gel filtration were lyophilized to remove the acetic acid and bidistilled in 4 ml H 2 0 each. added. Fig. 2 shows the inhibition of endothelial cell proliferation in the fractions after gel filtration. (S) and (M) represent the cell numbers at the time of sample application and after the maximum proliferation. The effect on endothelial cell proliferation triggered by aliquots from fractions 5-24 is shown by the corresponding column height.
- Fig. 3 shows a separation of aliquots from fractions 11-17 by SDS-PAGE and subsequent silver staining. Several bands are visible, the molecular weights of which are between 2.5 and 20 kDa. On the basis of the band pattern, fractions 11-13 are summarized for the further course of the isolation, which in addition to a broad band between 2 and 6 kDa (EMBIN I), a prominent band at 13 kDa and several showed weaker gangs. The same procedure was used for fractions 14 and 15 which, in addition to a band at 13 kDa, showed a broad band in the range between 14 and 20 kDa (ANEMIN).
- the data system 450 consists of an AT computer with implemented control software, as well as software for recording and processing the registered data.
- the separated substances were generally detected simultaneously at two wavelengths (in the region of the absorption of the peptide bond at a wavelength between 214 and 220 nm, and at 280 nm, the absorption maximum of tyrosine).
- Vydac 214 TP / 4.6 x 250 Aquapore 300 / 4.6 x 100 Asahipak ODP50 / 6 x 150 Spherisorb ODS2 / 4.6 x 250
- Fig. 4 shows the elution profile of an RP-HPLC using the Asahipak ODP50 column (C18 assignment) as an example. From the gel electrophoretic analysis "of the individual fractions it was evident that the inhibitory activity is in fraction 3 (shown by hatching). A gel electrophoretic analysis shows a band with a molecular weight of 2.5 to 6.5 kDa, which is EMBIN I.
- Buffer A 10 mM Tris, adjusted to pH 12.5 with 5N NaOH.
- Buffer B 10 mM Tris pH 10/80% acetonitrile
- Fig. 5 shows the elution of a sample containing EMBIN I at pH 12.5.
- the active fraction (determined by the BAEC test) is shown hatched.
- the inhibiting fraction showed the EMBIN I band in the molecular weight range from 2.5 to 6.2 kDa.
- EMBIN I The last purification step of EMBIN I was carried out on a 6 x 150 mm Asahipak ODP C18 column (Asahi Chemical Industry, Japan).
- EBMIN I-containing fractions from the gel filtration were dried in a vacuum concentrator and taken up in 5 mM heptanesulfonic acid pH 2.5 (Regis Chemical Company, Morton Grove, Illinois, or Fluka Chemika ⁇ lien, Ulm). 1 ml aliquots were applied to the column (equilibrated in 5 mM heptanesulfonic acid pH 2.5), the elution was carried out with a linear gradient from 0 to 100% 5 mM heptanesulfonic acid pH 2.5 in 90% acetonitrile for 35 min. The fractionated eluate was freed from the solvent in a vacuum concentrator and the residues were dissolved in at least. Water added for further analysis.
- Fig. 6 shows the elution profile of an EMBIN I-containing sample in RP-HPLC in the presence of heptanesulfonic acid as ion pair images.
- the fractions positive in the activity test (shown as hatched area) showed the EMBIN I band when separated by gel electrophoresis.
- Fig. 7 shows the elution profile of ANEMIN in RP-HPLC with heptanesulfonic acid.
- the fractions positive in the BAEC activity test are shown as hatched areas.
- the lyophilized fractions 14 and 15 from the gel filtration were taken up in 2 ml of the equilibration buffer and • separated under the same conditions as above.
- EMBIN I was also present in these fractions.
- Fig. 8 shows an SDS polyacrylamide gel of fractions 22-37 from the RP HPLC from ANEMIN. Aliquots from each fraction were separated on a gel and the peptide bands visualized by silver staining. The ANEMIN band in the range between 16 and 20 kDa was therefore contained in fractions 25 to 29, while EMBIN I was still visible in fractions 31 and 32.
- the diafiltered YC05 retentate was used as the substrate before or after gel filtration chromatography on BioGel P2.
- the following proteases were used to try to inactivate the inhibitory activity of EMBIN I:
- the proteases were dissolved in the buffers required in each case and incubated in an aliquot of the EMBIN I substrate under the conditions specified for the enzyme in question.
- BSA or lysozyme were incubated in parallel experiments with the proteases and the degradation of the proteins was checked by SDS PAGE.
- the proteases were inactivated by heating the mixture to 95 ° C. for 5 min, this was filtered sterile and checked for the inactivation of EMBIN I in the BAEC test.
- a positive control a corresponding aliquot of EMBIN I without enzyme, but with the volume of digestive agent used in the different batches, was incubated under the same conditions and tested in the BAEC test.
- Sequential digestion with Neura inidase and ⁇ -galactosidase 500 ⁇ l of the desalted YC05 retentate were adjusted to pH 5.0 with 29 ⁇ l of a 700 mM sodium acetate buffer and digested with 1 U neuraminidase (type X; Sigma) at 37 ° C. for 24 h .
- the residue was taken up in 500 ⁇ l of 50 mM Tris / HCl buffer pH 7.3 and magnesium chloride was added (10 M final concentration). 250 ⁇ l were removed for the gel electrophoretic analysis and the proliferation test, the rest was incubated with 10 U ⁇ -galactosidase (Sigma) for 18 hours at 37 ° C. After lyophilization, it was taken up in 250 ⁇ l dist. Water and checking the sample in the proliferation test.
- a mixture of 50 .mu.l of methanol and 25 .mu.l of chloroform was added to 20 .mu.l of a fraction which had an inhibitory effect after gel filtration on BioGel P2 and mixed thoroughly and extracted overnight at 4 ° C.
- 40 ⁇ l of a water / chloroform mixture (1: 1, v: v) was added to initiate phase separation. After a short centrifuge, the two phases were separated, rotated in the Speedvac and taken up in the initial volume for gel electrophoresis.
- the hydrolysates were transferred to 1.5 ml Eppendorf tubes and dried in a vacuum concentrator.
- the . Residues were taken up in 100 ul 0.1 M sodium hydrogen carbonate buffer pH 8.3. 250 ⁇ l of the dabsyl chloride solution were pipetted into each derivatization batch, a light red precipitate occurring. When it is subsequently heated to 70 ° C. in a water bath (12 min), this precipitate dissolves again, and a color change from light red to orange to yellow can be observed.
- the samples were cooled to room temperature and then by adding 650 ⁇ l 50 mM potassium phosphate / ethanol buffer pH 7.0 (1: 1, v: v) adjusted to a final volume of 1 ml. Smaller, flaky precipitates, which were present in individual samples, were removed by centrifugation in a Beckmann bench-top centrifuge for 5 minutes.
- the chromatographic separation of the derivatized amino acids was carried out on an HPLC system from the Kontron company with 2 HPLC pumps of the 420 type, a detector 430 and the data processing system 450.
- the detection of A ino- acid derivatives took place at 436 nm.
- the volume of the installed sample loop was 75 ⁇ l.
- a C18 Ultrasphere ODS column (4.6 x 250 mm or 4.6 x 150 mm) from Beckmann was used as the separation column, which is packed with 5 ⁇ particles.
- composition of the mobile phases A and B was based on the working instructions published by Beckmann for their "Dabs-Amino Acid Kit". Starting from a citric acid stock solution with 1 mol / 1, a 0.1 M stock solution was first prepared, the pH was adjusted to 6.5 with 5 N NaOH.
- the buffers were prepared as follows: A: 150 ml 0.1 M sodium citrate pH 6.5
- amino acids were separated by eluting the separation column with a multilinear gradient at a flow rate of 1.4 ml / min:
- the amounts of amino acids found are at the detection limit of this method.
- the characteristic peaks of serine, threonine, arginine, glycine and alanine are present in the chromatograph, as are the peaks of iso- leucine, phenylalanine and tyrosine.
- no evidence of the presence of rare amino acids could be obtained from the available chromatograms.
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- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Peptides Or Proteins (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US08/108,573 US5529792A (en) | 1991-03-01 | 1992-02-27 | Inhibitors of endothelial cell proliferation |
JP4504946A JPH06505243A (ja) | 1991-03-01 | 1992-02-27 | 内皮細胞の増殖に対する新規抑制因子 |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE4106570A DE4106570A1 (de) | 1991-03-01 | 1991-03-01 | Neue inhibitoren der endothelzell-proliferation |
DEP4106570.0 | 1991-03-01 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO1992015606A1 true WO1992015606A1 (de) | 1992-09-17 |
Family
ID=6426251
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1992/000419 WO1992015606A1 (de) | 1991-03-01 | 1992-02-27 | Neue inhibitoren der endothelzell-proliferation |
Country Status (5)
Country | Link |
---|---|
US (1) | US5529792A (de) |
EP (1) | EP0580594A1 (de) |
JP (1) | JPH06505243A (de) |
DE (1) | DE4106570A1 (de) |
WO (1) | WO1992015606A1 (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7875465B2 (en) | 2005-05-31 | 2011-01-25 | Canon Kabushiki Kaisha | Target substance capturing molecule |
US7989219B2 (en) | 2005-05-31 | 2011-08-02 | Canon Kabushiki Kaisha | Bispecific capturing molecule |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5648340A (en) * | 1991-10-31 | 1997-07-15 | Barnea; Eytan R. | Gestational agents for controlling cell proliferation |
KR100760367B1 (ko) * | 2000-02-15 | 2007-10-04 | 오보 바이오사이언시즈 인코포레이티드 | 난각내 조류 알의 알내 활성화 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0312246A2 (de) * | 1987-10-13 | 1989-04-19 | The Children's Medical Center Corporation | Angiogeneseinhibitor |
EP0398817A1 (de) * | 1989-05-19 | 1990-11-22 | Hadassah Medical Organization | Interleukin-1-Inhibitor |
WO1991011193A1 (en) * | 1990-01-25 | 1991-08-08 | Children's Hospital | Method and compositions for inhibiting angiogenesis |
-
1991
- 1991-03-01 DE DE4106570A patent/DE4106570A1/de not_active Withdrawn
-
1992
- 1992-02-27 WO PCT/EP1992/000419 patent/WO1992015606A1/de not_active Application Discontinuation
- 1992-02-27 US US08/108,573 patent/US5529792A/en not_active Expired - Fee Related
- 1992-02-27 EP EP92905215A patent/EP0580594A1/de not_active Withdrawn
- 1992-02-27 JP JP4504946A patent/JPH06505243A/ja active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0312246A2 (de) * | 1987-10-13 | 1989-04-19 | The Children's Medical Center Corporation | Angiogeneseinhibitor |
EP0398817A1 (de) * | 1989-05-19 | 1990-11-22 | Hadassah Medical Organization | Interleukin-1-Inhibitor |
WO1991011193A1 (en) * | 1990-01-25 | 1991-08-08 | Children's Hospital | Method and compositions for inhibiting angiogenesis |
Non-Patent Citations (4)
Title |
---|
European Journal of Immunology, Band 20, 1990, (Weinheim, DE), P. SECKINGER et al.: "Tumor necrosis factor inhibitor: purification, NH2-terminal amino acid sequence and evidence for anti-inflammatory and immunomodulatory activities", Seiten 1167-1174 * |
Experimental Cell Research, Band 188, Nr. 2, Juni 1990, (New York, US), D. VILETTE et al.: "Identification of an endothelial cell growth-inhibitory activity produced by human monocytes", Seiten 219-225, siehe Zusammenfassung * |
Journal of Cellular Biochemistry, Suppl. 0, Nr. 14, Teil C, 1990, (New York, US), H. DREXLER et al.: "Natural inhibitors of endothelial cell proliferation", siehe Seite 302, Zusammenfassung Nr. 1404, siehe Zusammenfassung * |
Science, Band 248, Nr. 4961, 15. Juni 1990, (Washington, DC, US), M.A. MOSES et al.: "Identification of an inhibitor of neovascularization from cartilage", Seiten 1408-1410, siehe das ganze Dokument * |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US7875465B2 (en) | 2005-05-31 | 2011-01-25 | Canon Kabushiki Kaisha | Target substance capturing molecule |
US7989219B2 (en) | 2005-05-31 | 2011-08-02 | Canon Kabushiki Kaisha | Bispecific capturing molecule |
Also Published As
Publication number | Publication date |
---|---|
EP0580594A1 (de) | 1994-02-02 |
JPH06505243A (ja) | 1994-06-16 |
DE4106570A1 (de) | 1992-09-03 |
US5529792A (en) | 1996-06-25 |
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