US20200406229A1 - Analytical method for sugar chains having acidic groups - Google Patents

Analytical method for sugar chains having acidic groups Download PDF

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US20200406229A1
US20200406229A1 US16/763,285 US201816763285A US2020406229A1 US 20200406229 A1 US20200406229 A1 US 20200406229A1 US 201816763285 A US201816763285 A US 201816763285A US 2020406229 A1 US2020406229 A1 US 2020406229A1
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column
carrier
sugar chain
chromatography
sample
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Tomoki FUKATSU
Chika MOROOKA
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JCR Pharmaceuticals Co Ltd
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    • B01J20/281—Sorbents specially adapted for preparative, analytical or investigative chromatography
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    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08—Selective adsorption, e.g. chromatography
    • B01D15/10—Selective adsorption, e.g. chromatography characterised by constructional or operational features
    • B01D15/18—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to flow patterns
    • B01D15/1864—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to flow patterns using two or more columns
    • B01D15/1871—Selective adsorption, e.g. chromatography characterised by constructional or operational features relating to flow patterns using two or more columns placed in series
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    • B01J20/32—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating
    • B01J20/3214—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the method for obtaining this coating or impregnating
    • B01J20/3217—Resulting in a chemical bond between the coating or impregnating layer and the carrier, support or substrate, e.g. a covalent bond
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    • B01J20/3231—Impregnating or coating ; Solid sorbent compositions obtained from processes involving impregnating or coating characterised by the coating or impregnating layer
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    • B01J20/3244—Non-macromolecular compounds
    • B01J20/3246—Non-macromolecular compounds having a well defined chemical structure
    • B01J20/3248—Non-macromolecular compounds having a well defined chemical structure the functional group or the linking, spacer or anchoring group as a whole comprising at least one type of heteroatom selected from a nitrogen, oxygen or sulfur, these atoms not being part of the carrier as such
    • B—PERFORMING OPERATIONS; TRANSPORTING
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    • B01J41/00—Anion exchange; Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
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    • B01J41/08—Use of material as anion exchangers; Treatment of material for improving the anion exchange properties
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    • B01J41/14—Macromolecular compounds obtained by reactions only involving unsaturated carbon-to-carbon bonds
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    • G01N30/28—Control of physical parameters of the fluid carrier
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    • G01N30/88—Integrated analysis systems specially adapted therefor, not covered by a single one of the groups G01N30/04 - G01N30/86
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
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    • G01N2030/8836—Integrated analysis systems specially adapted therefor, not covered by a single one of the groups G01N30/04 - G01N30/86 analysis specially adapted for the sample biological materials involving saccharides

Definitions

  • the present invention relates to a method for separating and analyzing acidic sugar chains having acidic groups, and more particularly, to a chromatography column which can be used for separating acidic sugar chains, and to a method for separating and analyzing sugar chains having acidic groups contained in glycoproteins using the chromatography column.
  • Non-Patent Document 1 As a method for analyzing the sugar chain structure of a glycoprotein, a method has been known in which a glycoprotein is trypsinized and treated with glycosidase to liberate sugar chains from the glycoprotein, and then this sugar chain is labeled with 2-aminopyridine (2-aminopyridine label), and subjected to normal phase column chromatography for separation analysis (Non-Patent Document 1).
  • the 2-aminopyridine labeling of a sugar chain is performed, for example, by adding a 2-aminopyridine solution to a sample containing a sugar chain and performing a heating reaction to form an imine, followed by adding a borane-dimethylamine complex solution and heating to reduce the imine (Non-Patent Document 1).
  • the method of labeling the sugar chain with 2-aminopyridine includes a step of evaporation for removing an organic solvent such as toluene which is harmful to the human body (Patent Document 1 and Non-Patent Document 2).
  • Non-Patent Document 1 Kuraya N. et. al., J. Biochem. 112. 122-6 (1992)
  • Non-Patent Document 2 Kondo A. et. al., Agric. Biol. Chem. 54. 2169-70 (1990)
  • An objective of the present invention is to provide a chromatography column for separating and analyzing acidic sugar chains having acidic groups such as phosphate groups and constituting glycoproteins, and a method for separating and analyzing acidic sugar chains using such a column.
  • acidic sugar chains constituting glycoproteins can be separated and analyzed sensitively by using, in one embodiment, a column for hydrophilic interaction chromatography (a column for normal phase column chromatography) in which silica having a surface modified to be hydrophobic and into the surface an amino alkyl group is introduced as a functional group is used as a carrier, and a column for hydrophilic interaction chromatography (column for normal phase column chromatography) in which polyvinyl alcohol is used as a base and a resin into which an amino group is introduced as a functional group is used as a carrier, thereby completing the present invention.
  • a column for hydrophilic interaction chromatography a column for normal phase column chromatography
  • silica having a surface modified to be hydrophobic and into the surface an amino alkyl group is introduced as a functional group is used as a carrier
  • a column for hydrophilic interaction chromatography column for hydrophilic interaction chromatography
  • polyvinyl alcohol is used as a base and a resin into
  • the present invention includes the following:
  • a chromatography column for the use of separating acidic sugar chains, wherein the column comprises a first column and a second column, the second column connected by a flow path downstream of an outlet of the first column, and selected from the following (1) or (2):
  • X represents a silica portion constituting the carrier 1
  • X represents the silica portion constituting the carrier 1
  • Y represents the resin portion constituting the carrier 2
  • n represents an integer of 1 to 8.
  • a method for separating acidic sugar chains includes:
  • an acidic sugar chain for example an acidic sugar chain excised from a glycoprotein by an enzyme, can be analyzed with high sensitivity.
  • FIG. 1 shows the results of analysis of acidic sugar chains using the sugar chain profiling mobile phase B adjusted to pH 2.5.
  • A represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 1 (chromatography condition 1)
  • B represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 1
  • C represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 2 (chromatography condition 2)
  • “D” represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 2, respectively.
  • Arrows 1 and 2 indicate peaks corresponding to phosphorylated sugar chains.
  • the vertical axis represents the fluorescence intensity (400 nm) and the horizontal axis represents the retention time, respectively.
  • FIG. 2 shows the results of analysis of acidic sugar chains using the sugar chain profiling mobile phase B adjusted to pH 3.0.
  • A represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 1 (chromatography condition 1)
  • B represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 1
  • C represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 2 (chromatography condition 2)
  • “D” represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 2, respectively.
  • Arrows 1 and 2 indicate peaks corresponding to phosphorylated sugar chains.
  • the vertical axis represents the fluorescence intensity (400 nm) and the horizontal axis represents the retention time, respectively.
  • FIG. 3 shows the results of analysis of acidic sugar chains using the sugar chain profiling mobile phase B adjusted to pH 3.5.
  • A represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 1 (chromatography condition 1)
  • B represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 1
  • C represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 2 (chromatography condition 2)
  • “D” represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 2, respectively.
  • Arrows 1 and 2 indicate peaks corresponding to phosphorylated sugar chains.
  • the vertical axis represents the fluorescence intensity (400 nm) and the horizontal axis represents the retention time, respectively.
  • FIG. 4 shows the results of analysis of acidic sugar chains using the sugar chain profiling mobile phase B adjusted to pH 2. 5.
  • A represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 1 (chromatography condition 1)
  • B represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 1
  • C represents a chromatogram obtained by analyzing a BAP-treated sample under column chromatography condition 2 (chromatography condition 2)
  • “D” represents a chromatogram obtained by analyzing a BAP-untreated sample under chromatography condition 2, respectively.
  • Arrows 1 and 2 indicate peaks corresponding to phosphorylated sugar chains.
  • the vertical axis represents the fluorescence intensity (400 nm) and the horizontal axis represents the retention time, respectively.
  • the term “acidic sugar chains” refers to sugar chains having acid groups such as sulfate groups, carboxyl groups, phosphate groups, and the like, including chondroitin 4-sulfate, chondroitin 6-sulfate, heparan sulfate, dermatan sulfate, keratan sulfate, and the like. Acidic sugar chains may also be included in the sugar chains that constitute the glycoprotein, and the glycoprotein has an important function in order for the glycoprotein to exert its function in the body. For example, an acidic sugar chain containing mannose-6-phosphate (M6P) at the reducing end of the sugar chain is essential for the uptake of the glycoprotein into the cell via the M6P receptor.
  • Glycoproteins to be uptaken into cells via receptors include, for example, lysosomal enzymes such as iduronate-2-sulfatase and ⁇ -galactosidase A.
  • the carrier of the column used as the carrier 1 in one embodiment of the present invention is a silica modified to be hydrophobic by introducing a hydrophobic group into the surface and having a group containing a primary amine, a secondary amine, or a tertiary amine.
  • the hydrophobic group introduced to modify the silica to be hydrophobic is not particularly limited, but is preferably an alkyl group such as a methyl group, an ethyl group, or a propyl group, and is particularly preferably a methyl group.
  • Such a hydrophobic group may be directly covalently bonded to a silicon atom constituting silica, or may be covalently bonded to a silicon atom via an oxygen atom.
  • the following general formula [I] is a suitable example of a silica modified with a hydrophobic group, in which three methyl groups are bonded to a silicon atom constituting the silica.
  • X represents a silica portion constituting the carrier 1.
  • a primary amine, a secondary amine, or/and a tertiary amine contained in a silica which is a carrier of the column used as the carrier 1, may be directly covalently bonded to a silicon atom constituting silica, or may be covalently bonded to a silicon atom via an oxygen atom.
  • the following general formula [II] is a suitable example of a silica modified with a primary amine.
  • X represents a silica portion constituting the carrier 1.
  • the carrier of the column used as the carrier 2 is a resin haying a group containing a primary amine, a secondary amine, or/and a tertiary amine.
  • the following general formula [III] is a suitable example of such a resin containing a primary amine and a secondary amine.
  • Y represents a resin portion constituting the carrier 2.
  • the resin constituting the carrier 2 is preferably a hydrophilic resin, and more preferably a resin based on polyvinyl alcohol or modified polyvinyl alcohol.
  • the carrier 2 preferably has a property as an anion exchange resin.
  • the chromatography column used for separating the acidic sugar chains is a column in which the carrier 1 is packed and a column in which the carrier 2 is packed are connected in series via a flow path.
  • the column located upstream of the flow path is referred to as a first column
  • the column located downstream is referred to as a second column.
  • the first column may be filled with the carrier 1 and the second column may be filled with the carrier 2, or the first column may be filled with the carrier 2 and the second column may be filled with the carrier 1.
  • a unit in which the second column is connected by a flow path downstream of the outlet of the first column constitutes a chromatography column used for separating acidic sugar chains. It is preferable that the first column and the second column each functions as a hydrophilic interaction chromatography column, hence a chromatography column having a configuration in which the first column and the second column are connected to each other functions as a hydrophilic interaction chromatography column as a whole.
  • the chromatography column having the configuration in which the first column and the second column are connected functions as a column for hydrophilic interaction chromatography as a whole
  • the hydrophilic sugar chains are retained on a carrier.
  • sugar chains are eluted from the column in descending order of hydrophobicity.
  • Acidic sugar chains are highly hydrophilic because they have sulfate groups, carboxyl groups, phosphate groups, and the like, thus are strongly retained in the column when loaded on a column for hydrophilic interaction chromatography. Therefore, according to the column of the present invention, the acidic sugar chain is selectively held in the column for a longer period of time, the separation capacity of acidic sugar chains is improved, and further, the acidic sugar chain can be analyzed with higher sensitivity by using it.
  • the mobile phase in column chromatography is gradually replaced from highly hydrophobic (low hydrophilic) to highly hydrophilic (low hydrophobic).
  • the mobile phase in column chromatography is gradually replaced from highly hydrophobic (low hydrophilic) to highly hydrophilic (low hydrophobic).
  • the mobile phase in column chromatography is gradually replaced from highly hydrophobic (low hydrophilic) to highly hydrophilic (low hydrophobic).
  • the mobile phase in column chromatography is gradually replaced from highly hydrophobic (low hydrophilic) to highly hydrophilic (low hydrophobic).
  • the mobile phase in column chromatography is gradually replaced from highly hydrophobic (low hydrophilic) to highly hydrophilic (low hydrophobic).
  • the pH of the second mobile phase is particularly important.
  • the pH of the second mobile phase is limited to the acidic side because of the need to coordinate protons to the amino groups of the carrier.
  • the sulfate group, carboxyl group, phosphate group, and the like contained in acidic sugar chains are dissociated into anions more in the mobile phase, so that they are strongly retained by the carrier having the amino group coordinated with the proton, and the time until they are eluted is prolonged. Therefore, by adjusting the pH of the second mobile phase within the acidic range, the peaks of the acidic sugar chains can be selectively separated.
  • the pH of the second mobile phase is preferably adjusted to pH of 2.0 to 6.0, more preferably to pH of 3.0 to 6.0, even more preferably to pH of 3.5 to 6.0, e.g., pH3.0, 3.5, 4.0, 4.5, 5.0 and a like.
  • the acidic sugar chain can be separated by using the chromatography column of the present invention, in order to detect the separated acidic sugar chain, it is preferable to fluorescently label the sugar chain contained in the sample in advance.
  • the method of fluorescent labeling is not particularly limited, but aminopyridine labeling is suitable.
  • an aldehyde group or a ketone group may be generated when a sugar having a cyclic structure is ring-opened to form a chain structure.
  • 2-amnopyridine labeling refers to producing an imine by reacting the reducing end of a sugar or sugar chain with 2-aminopyridine and subsequently adding 2-aminopyridine to the reducing end of a sugar or sugar chain by reducing the imine with a borane-dimethylamine complex or the like.
  • a 2-aminopyridine labeled sugar chain, an aminopyridine labeled sugar chain, or a labeled sugar chain refers to a sugar or sugar chain labeled with 2-aminopyridine (or labeled with an aminopyridine).
  • Aminopyridine-labeled sugar chains can be analyzed by loading them onto the chromatography column of the present invention, and continuously irradiating the solution after passing through the column with excitation light by using a fluorescence detector, and measuring the intensity of fluorescence emitted from the effluent.
  • the excitation light thus irradiated is ultraviolet light at a wavelength of 300 to 340 nm, for example, ultraviolet light at a wavelength of 320 nm.
  • the fluorescence thus emitted is measured by a fluorescence detector as ultraviolet light at a wavelength of 300 to 340 nm, for example, as ultraviolet light at a wavelength of 320 nm.
  • the acidic sugar chain to be analyzed constitutes a part of the glycoprotein
  • the excision of the sugar chain from the glycoprotein is performed by enzyme treatment or chemical treatment.
  • the enzyme treatment is performed using N-glycosidase, glycopeptidase A, O-glycosidase, or the like, and the chemical treatment is performed by hydrazine degradation or the like.
  • An example of a method for identifying peaks corresponding to acidic sugar chains on a chromatogram resulting from column chromatography is shown below.
  • the sample is divided, and one part is treated with an enzyme having an activity of cleaving an acidic group contained in the acidic sugar chain from the sugar chain.
  • the sample is then loaded onto column chromatography and the chromatogram obtained by analyzing the sugar chains untreated with the enzyme (enzyme untreated chromatogram) is compared with the chromatogram obtained by analyzing the sugar chains treated with the enzyme (enzyme treated chromatogram), and the peak detected on the enzyme untreated chromatogram but disappearing in the enzyme treated chromatogram can be identified as the peak corresponding to the acidic sugar chains.
  • Sulfate groups can be cleaved using sulfatase, carboxyl groups can be cleaved using decarboxylase, and phosphate groups can be cleaved using phosphatase from acidic sugar chains, respectively.
  • Glycoproteins of which the sugar chain is to be analyzed include, but are not limited to, lysosomal enzymes such as iduronate-2-sulfatase, cx-galactosidase A, acid sphingomyelinase, ⁇ -L-iduronidase, N-acetylgalactosamine-4-sulfatase, glucocerebrosidase (glucosylceramidase), galsulfase, lysosomal acid lipase, acid ⁇ -glucosidase, tissue plasminogen activator (t-PA), blood coagulation factor such as blood coagulation factor VII, blood coagulation factor VIII, blood coagulation factor IX, erythropoietin, interferon, thrombomodulin, follicle-stimulating hormones, thyroid-stimulating hormones, GM-CSF, G-CSF, M-CSF, and antibodies, in particular,
  • Lysosomal enzymes such as iduronate-2-sulfatase and ⁇ -galactosidase A have acidic sugar chains modified with mannose-6-phosphate (M6P). Therefore, the sugar chain containing M6P of the lysosomal enzymes can be identified by excising the sugar chain from the lysosome, treating one part of the sugar chain with phosphatase, and comparing the chromatogram between the phosphatase-treated and the untreated chains.
  • M6P mannose-6-phosphate
  • Expression vectors for hI2S-humanized anti-hTfR antibody fusion protein were constructed using genetic sequences coding a humanized anti-hTfR antibody comprising a light chain having the amino acid sequences set forth as SEQ ID NO:1 and a heavy chain having the amino acid sequences set forth as SEQ ID NO:2.
  • a pEF/myc/nuc vector (Invitrogen Inc.) was digested with KpnI and NcoI to cut out the region containing the EF-1 ⁇ promoter and its first intron, and the region was blunt-ended with T4 DNA polymerase.
  • a pCI-neo (Invitrogen Inc.) was digested with BglII and EcoRI to cut out the region containing the enhancer/promoter and intron of CMV, and then the region was blunt-ended with T4 DNA polymerase. The above region containing the EF-1 ⁇ promoter and its first intron was inserted into this to construct a pE-neo vector.
  • the pE-neo vector was digested with SfiI and BstXI and a region of approximately 1 kbp containing the neomycin resistance gene was cut out.
  • Amplification of hygromycin gene was carried out by PCR reaction using primers Hyg-Sfi5′ (SEQ ID NO:3) and Hyg-BstX3′ (SEQ ID NO:4) and using pcDNA 3.1/Hygro (+)(Invitrogen Inc.) as a template.
  • the amplified hygromycin gene was digested with SfiI and BstXI and inserted into the pE-neo vector from which the above neomycin resistance gene has been cut out to construct a pE-hygr vector.
  • a DNA fragment (SEQ ID NO:5) containing the gene encoding the full length of the light chain of the humanized anti-hTfR antibody having the amino acid sequence set forth as SEQ ID NO:1 was synthesized.
  • a MluI sequence was introduced on the 5′ side of this DNA fragment and a NotI sequence on the 3′ side thereof.
  • This DNA fragment was digested with MluI and NotI and incorporated between MluI and Not of the pE-neo vector.
  • the obtained vector was designated pE-hygr(LC) which is a vector for expressing the light chain of humanized anti-hTfR antibody.
  • a DNA fragment was artificially synthesized, having a nucleotide sequence set forth as SEQ ID NO:7 containing a gene encoding a protein in which hI2S having an amino acid sequence set forth as SEQ ID NO:6 is linked to the C-terminal side of the heavy chain of the humanized anti-hTfR antibody having an amino acid sequence set forth as SEQ ID NO:2 via a linker having an amino acid sequence set forth as (Gly-Ser).
  • This DNA fragment encodes a protein having the amino acid sequence set forth as SEQ ID NO:8, in which a heavy chain of humanized anti-hTfR antibody binds to hI2S.
  • This DNA fragment was digested with MluI and NotI and inserted between MluI and Not of the pE-neo vector to construct pE-neo (HC-I2S).
  • CHO cells (CHO-K1 obtained from American Type Culture Collection) were transformed with combinations of pE-hygr (LC) and pE-neo (HC-I2S) constructed in Example 2 using the GenePulser (Bio-Rad Inc.). Transformation of cells was in brief carried out by the following method.
  • CHO-K1 cells 5 ⁇ 10 5 CHO-K1 cells were seeded in a 3.5 cm culture dish to which CD OptiCHOTM medium (Thermo. Fisher Scientific Inc.) was added and cultured overnight at 37° C. under 5% CO 2. After the culture, the cells were suspended in Opti-MEMTM I medium (Thermo Fisher Scientific Inc.) to a density of 5 ⁇ 10 6 cells/mL. 100 ⁇ L of the cell suspension was collected, and thereto 5 ⁇ L each of the pE-hygr (LC) and pE-neo (HC-I2S) plasmid DNA solutions both having been diluted to 100 ⁇ g/mL with CD OptiCHOTM medium was added.
  • CD OptiCHOTM medium Thermo. Fisher Scientific Inc.
  • Electroporation was performed using GenePulser (Bio-Rad Inc.) to introduce the plasmids into the cells. After overnight culture under the condition of 37° C., 5% CO 2 , the cells were selectively cultured in CD OptiCHOTM medium supplemented with 0.5 mg/mL of hygromycin and 0.8 mg/mL of G418.
  • the cells selected above through the selection culture were seeded on 96-well plates so that not more than one cell might be seeded per well by limiting dilution.
  • the cells than were cultured for about 10 days so that monoclonal colonies formed.
  • Respective culture supernatants of the wells in which monoclonal colony formed were collected, the amount of the humanized antibody contained in culture supernatants was determined by ELISA, and the hI2S-humanized anti-hTfR antibody fusion protein high-expressing cell lines were selected.
  • the ELISA above was conducted as follows in general. To each well of 96-well microtiter plates (Nunc Inc.) was added 100 ⁇ L of a goat anti-human IgG polyclonal antibody solution diluted with 0.05 M sodium bicarbonate buffer (pH 9.6) to 4 ⁇ g/mL, and the plate was left to stand for at least one hour at room temperature so as to allow the antibody to be adsorbed by the plates.
  • a goat anti-human IgG polyclonal antibody solution diluted with 0.05 M sodium bicarbonate buffer (pH 9.6) to 4 ⁇ g/mL
  • the culture supernatant or the human IgG reference standard product which had been diluted with a phosphate buffer saline (pH 7.4) supplemented with 0.5% BSA and 0.05% Tween20 (PBS-BT) to appropriate concentrations, was added to each well, in the amount of 100 ⁇ L, and the plates were left to stand for at least one hour at room temperature.
  • 100 ⁇ L of HRP-labeled anti-human IgG polyclonal antibody solution which had been diluted with PBS-BT, was added to each well, and the plates were left to stand for at least one hour at room temperature.
  • citrate-phosphate buffer pH 5.0
  • o-phenylenediamine containing 0.4 mg/mL o-phenylenediamine was added to each well, in the amount of 100 ⁇ L, and the wells were left to stand for 8 to 20 minutes at room temperature.
  • 1 mol/L sulfuric acid was added to each well in the amount of 100 ⁇ L to terminate the reaction, and the absorbance for each well was measured at 490 nm using a 96-well plate reader.
  • the cells corresponding to the wells which exhibited the higher measurements were regarded as a high-expressing cell line for hI2S-humanized anti-hTfR antibody fusion protein.
  • the hI2S-humanized anti-hTfR antibody fusion protein expressed by this cell line was designated as I2S-anti-hTfR antibody.
  • the hI2S-anti-hTfR antibodies were produced by the method described below.
  • the hI2S-anti-hTfR antibody expressing strain obtained in Example 3 was suspended in about 200 L of serum-free medium (EX-CELL Advanced CHO Fed-batch Medium, Sigma Aldrich Inc.) containing 4 mM L-alanyl-L-glutamine, 100 ⁇ mol/L hypoxanthine and 16 ⁇ mol/L thymidine to the density of about 2/10 5 cells/mL. 140 L of this cell suspension was transferred to a culture tank. The cells were cultured for about 11 days at a temperature range of 34 to 37° C., while the medium was stirred with an impeller, and the dissolved oxygen saturation of the medium was kept at about 40%.
  • the culture supernatant was subjected to ultrafiltration using a PelliconTM 3 Cassette w/Ultracel PLCTK Membrane (pore size: 30 kDa, membrane area: 1.14 m 2 , Merck Inc.).
  • the concentrate was then filtered using OpticapXL600 (0.22 ⁇ m, Merck Inc.). The obtained solution was used as a concentrated culture supernatant.
  • the concentrated culture supernatant was filtrated by a Millipak-200 Filter Unit (pore size: 0.22 ⁇ m, Merck Inc.) after adding thereto 20 mM Tris-HCl buffer (pH 7.0) containing 0.5 volume of 140 mM NaCl.
  • the solution after filtration was loaded onto a MabSelect SuRe LX column (column volume: about 3.2 L, bed height: about 20 cm, GE Healthcare Inc.), which was a protein A affinity column, and equilibrated with 4 column volumes of 20 mM Tris-HCl buffer (pH 7.0) containing 140 mM NaCl, at a constant flow rate of 200 cm/hour to adsorb I2S-anti-hTfR antibody to protein A.
  • the column was washed with 5 column volumes of 10 mM Tris-HCl buffer (pH 7.0) containing 500 mM NaCl and 450 mM arginine at the same flow rate. Then the column was further washed with 2.5 column volumes of 20 mM Tris-HCl buffer (pH 7.0) containing 140 mM NaCl at the same flow rate. Then I2S- anti-hTfR antibody 3 adsorbed to Protein A was eluted with 5 column volumes of 100 mM glycine buffer (pH 3.5) containing 140 mM NaCl. The eluate was immediately neutralized by 1 M Tris-HCl buffer (pH 7.5).
  • I2S-anti-hTfR antibody The fractions which corresponded to an absorption peak at 280 nm were collected as a fractions containing I2S-anti-hTfR antibody, which was designated as a purified product of I2S-anti-hTfR antibody (hereinafter, I2S-anti-hTfR antibody).
  • 0.2 mg of the I2S-anti hTfR antibody obtained in Example 5 above was collected and dried under reduced pressure, dissolved in 50 ⁇ l of a protein lysis solution (a solution prepared by dissolving 66.8 g of guanidine hydrochloride, 6.1 g of tris(hydroxymethyl) aminomethane and 0.372 g of disodium ethylenediamine tetraacetate in water, adjusted to pH 8.5 with 1 N hydrochloric acid, and adding water to make the volume 100 mL).
  • 4 ⁇ L of the reduction solution (10 mg of dithiothreitol dissolved in 50 ⁇ L of protein lysate) was then added, shaken, and allowed to stand at room temperature for 30 minutes.
  • iodoacetic acid solution 25 mg of iodoacetic acid dissolved in 60 ⁇ L of 1 N aqueous sodium hydroxide solution
  • the reactant was then subjected to gel-filtration column chromatography to separate fractions containing I2S-anti hTfR antibody.
  • the gel-filtration column chromatography was carried out by applying the reactant to a Sephadex (registered trademark) G-25 superfine (column diameter: 5 mm, column length: 150 mm, GE Healthcare Inc.) equilibrated with pure water, flowing water at a flow rate of 1 mL/min at room temperature, and monitoring the absorbance at a wavelength of 215 nm with an ultraviolet absorbance spectrophotometer.
  • the fraction containing I2S-anti hTfR antibody was separated and dried under reduced pressure.
  • Example 7 To the reactant of trypsinization obtained in Example 7 above, 5 ⁇ L of a glycosidase solution (N-glycosidase dissolved in pure water at a concentration of 1,000 units/mL) was added, and the solution was allowed to stand at degrees for 3 hours for reaction. The solution was then heated at degrees for 5 minutes to deactivate the glycosidase. The resulting solution was used as a glycosidase digest.
  • a glycosidase solution N-glycosidase dissolved in pure water at a concentration of 1,000 units/mL
  • the gel filtration column chromatography was carried out by applying a sugar chain dissolving solution and subsequently 0.1% (v/v) acetic acid aqueous solution to SEPHADEXTM G-15 (column inner diameter: 28 mm, column length: 200 mm, GE Healthcare Inc.) equilibrated with pure water at flow rate of 8 mL/min at room temperature, with the fluorescence intensity monitored with a fluorescence detector (excitation wavelength: 320 nm, fluorescence wavelength: 400 nm).
  • the fractions corresponding to the peak appearing between and 10 minutes after applying the sugar chain dissolving solution onto the column were collected as a fraction containing aminopyridine-labeled sugar chains. The collected fractions were dried under reduced pressure.
  • Example 9 1 mL of pure water was added to the dried product obtained in Example 9 under reduced pressure and the product was dissolved. This solution was dispensed into two 0.5 mL tubes, dried under reduced pressure, and dissolved in 80 ⁇ L of pure water. To a new tube, 52 ⁇ L of the lysis solution was dispensed. In this tube, 1 unit of alkaline phosphatase (Takara Bio Inc.) and 6 ⁇ L of reaction buffer (500 mM Tris-HCl (pH 9.0) containing 10 mM MgCl 2 ) was added and mixed, and the mixture was allowed to react at 50 degrees for 1 hour.
  • reaction buffer 500 mM Tris-HCl (pH 9.0) containing 10 mM MgCl 2
  • Example 10 The BAP-treated sample and the BAP-untreated sample obtained in Example 10 were loaded onto a column under the following conditions (column chromatography condition and column chromatography condition 2), and the sugar chains contained in each sample were separated and analyzed.
  • Sugar chain profiling mobile phase A and sugar chain profiling mobile phase B were 18 prepared in Example 1.
  • AsahipakTM NH2P-50 4E is a hydrophilic interaction chromatography column (normal phase chromatography column) using a resin based on polyvinyl alcohol into which an amino group is introduced as a functional group as a carrier.
  • TSKgel NH2-100 is a hydrophilic interaction chromatography column (normal phase chromatography column) using silica having a surface modified to be hydrophobic on which an aminoalkyl group introduced as a functional group as a carrier.
  • the acidic sugar chains contained in the sugar chains can be detected with higher sensitivity by combining a hydrophilic interaction chromatography column (normal phase column chromatography column) using a resin, the based on polyvinyl alcohol into which an amino group is introduced as a functional group, as a carrier, and a hydrophilic interaction chromatography column (normal phase column chromatography column) using silica having a surface modified to be hydrophobic on which an aminoalkyl group introduced as a functional group as a carrier.
  • a hydrophilic interaction chromatography column normal phase column chromatography column
  • silica having a surface modified to be hydrophobic on which an aminoalkyl group introduced as a functional group as a carrier.
  • a chromatography column capable of analyzing acidic sugar chains, for example acidic sugar chains excised from glycoproteins by an enzyme, with high sensitivity, and a method for analyzing acidic sugar chains using the column.
  • SEQ ID NO: 1 Amino acid sequence of the light-chain of humanize d anti-hTfR antibody
  • SEQ ID NO: 2 Amino acid sequence of the heavy-chain of humanize d anti-hTfR antibody
  • SEQ ID NO:3 Primer Hyg-Sfi5′, synthetic sequence
  • SEQ ID NO:4 Primer Hyg-BstX3′, synthetic sequence
  • SEQ ID NO:5 Nucleic acid sequence containing nucleic acid sequence encoding the light-chain of humanized anti-hTfR antibody, synthetic sequence
  • SEQ ID NO:7 Nucleotide sequence encoding the fused protein of the heavy-chain of humanized anti-hTfR antibody and hI2S, synthetic sequence
  • SEQ ID NO: 8 Amino acid sequence of fused protein of the heavy-chain of humanized anti-hTfR antibody and hI2S

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