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公开(公告)号:US20180215796A1
公开(公告)日:2018-08-02
申请号:US15876610
申请日:2018-01-22
Applicant: Kaneka Corporation
Inventor: Masakatsu Nishihachijyo , Yoshiyuki Nakano , Fuminori Konoike , Masayuki Takano , Shinichi Yoshida , Kazunobu Minakuchi
CPC classification number: C07K14/31 , B01D15/3809 , B01J20/286 , B01J20/3274 , C07K1/22 , C07K17/00 , C07K2319/30
Abstract: A protein includes an amino acid sequence derived from a sequence selected from the group consisting of SEQ ID NOs: 1 to 5. The amino acid sequence includes a substitution of a hydrophobic amino acid residue, an acidic amino acid residue, or a polar uncharged amino acid residue with a basic amino acid residue, and the protein has a reduced antibody-binding capacity in an acidic pH range, as compared to a protein including the amino acid sequence without the substitution.
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2.
公开(公告)号:US20180215795A1
公开(公告)日:2018-08-02
申请号:US15876597
申请日:2018-01-22
Applicant: Kaneka Corporation
Inventor: Masakatsu Nishihachijyo , Yoshiyuki Nakano , Fuminori Konoike , Masayuki Takano , Shinichi Yoshida , Kazunobu Minakuchi
CPC classification number: C07K14/31 , C07K1/22 , C07K14/195 , C07K17/00 , C07K19/00 , C07K2319/30 , C12N5/10 , C12N15/09
Abstract: A protein includes an amino acid sequence derived from a sequence selected from the group consisting of SEQ ID NOs: 1 to 5. The amino acid sequence includes a substitution of a hydrophobic amino acid residue in an Fc binding site with a different hydrophobic amino acid residue or a polar uncharged amino acid residue, and the protein has a reduced antibody-binding capacity in an acidic pH range, as compared to a protein including the amino acid sequence without the substitution.
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公开(公告)号:US20180215835A1
公开(公告)日:2018-08-02
申请号:US15876604
申请日:2018-01-22
Applicant: Kaneka Corporation
Inventor: Masakatsu Nishihachijyo , Yoshiyuki Nakano , Fuminori Konoike , Masayuki Takano , Shinichi Yoshida , Kazunobu Minakuchi
CPC classification number: C07K17/02 , B01D15/3809 , C07B2200/11 , C07K1/22 , C07K14/31 , C07K16/065 , C07K2317/52 , C07K2317/92 , C07K2318/20
Abstract: A protein includes an amino acid sequence derived from the sequence of SEQ ID NO: 1, wherein the amino acid sequence includes a substitution of Val at a position corresponding to position 40 of SEQ ID NO: 1 with a polar uncharged amino acid residue, a basic amino acid residue, or Ala. The protein has a reduced antibody-binding capacity in an acidic pH range, as compared to a protein including the amino acid sequence without the substitution.
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4.
公开(公告)号:US20210024433A1
公开(公告)日:2021-01-28
申请号:US17039471
申请日:2020-09-30
Applicant: KANEKA CORPORATION
Inventor: Takayuki Asada , Yoshiyuki Nakano , Toyoaki Watanabe , Ken Uekita
IPC: C05G5/10
Abstract: One or more embodiments of the present invention provide an oxidized glutathione-containing solid composition which can be produced by a simple method and has low deliquescence and is easy to handle. One or more embodiments of the present invention relate to a solid composition comprising an amorphous oxidized glutathione and a water-soluble cellulose derivative. One or more embodiments of the present invention also relate to a method for producing the solid composition comprising an amorphous oxidized glutathione and a water-soluble cellulose derivative, comprising a step of drying a solution comprising oxidized glutathione and a water-soluble cellulose derivative dissolved in an aqueous solvent.
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5.
公开(公告)号:US20190263870A1
公开(公告)日:2019-08-29
申请号:US16298639
申请日:2019-03-11
Applicant: KANEKA CORPORATION
Inventor: Shinichi Yoshida , Dai Murata , Shunichi Taira , Masayuki Takano , Keita Iguchi , Yoshiyuki Nakano
IPC: C07K14/195 , C07K16/32 , C07K14/31 , C07K16/06 , C07K1/22
Abstract: An object of the present invention is to create a novel engineered Protein A ligand having better antibody dissociation properties in the acidic condition compared with known engineered Protein A ligands. The present invention provides a protein having an affinity for an immunoglobulin, including an amino acid sequence obtained by introducing, into an amino acid sequence derived from any of E, D, A, B and C domains of Protein A, at least one amino acid substitution at any one or more of amino acid residues corresponding to positions 31 to 37 of the A, B and C domains (positions 29 to 35 of the E domain, positions 34 to 40 of the D domain), which are conserved in all the domains, the protein having a lower affinity for an Fab region of an immunoglobulin than a protein having the amino acid sequence before introduction of the substitution.
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公开(公告)号:US20180215836A1
公开(公告)日:2018-08-02
申请号:US15883569
申请日:2018-01-30
Applicant: Kaneka Corporation
Inventor: Masakatsu Nishihachijyo , Fuminori Konoike , Yoshiyuki Nakano , Masayuki Takano , Keita Yamashita
CPC classification number: C07K17/02 , B01D15/3809 , B01J20/286 , B01J20/3204 , B01J20/321 , B01J20/3274 , C07K1/22 , C07K14/31 , C07K16/065 , C07K16/42 , C07K2317/52 , C07K2317/92 , C12N15/09
Abstract: A protein includes two or more amino acid sequences, wherein each amino acid sequence is derived from a sequence selected from the group consisting of SEQ ID NOs: 1 to 5. The amino acid sequence closest to the N-terminus includes more Lys residues than the other amino acid sequence(s), and in the amino acid sequence closest to the N-terminus, a total number of Lys in positions 1 to 38 is equal to or greater than a total number of Lys in position 39 and subsequent positions.
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公开(公告)号:US20180215785A1
公开(公告)日:2018-08-02
申请号:US15876615
申请日:2018-01-22
Applicant: Kaneka Corporation
Inventor: Masakatsu Nishihachijyo , Yoshiyuki Nakano , Fuminori Konoike , Masayuki Takano , Shinichi Yoshida , Kazunobu Minakuchi
CPC classification number: C07K1/22 , B01D15/168 , B01D15/3809 , B01J20/286 , B01J20/3212 , B01J20/3219 , B01J20/3274 , C07K14/31 , C07K17/02
Abstract: A method for purifying an antibody-like protein includes adsorbing an antibody-like protein onto an affinity separation matrix by bringing the antibody-like protein into contact with the affinity separation matrix; and eluting the antibody-like protein by bringing an eluent having a pH of 3.5 or higher into contact with the affinity separation matrix. The affinity separation matrix includes a carrier and a ligand immobilized on the carrier, and the ligand includes an amino acid sequence derived from a sequence selected from the group consisting of SEQ ID Nos: 1 to 5. Gln or Lys in an Fc-binding site of the amino acid sequence is substituted by Ala, Ser, or Thr, and the ligand has a lower antibody-binding capacity in an acidic pH range, as compared to a ligand including the amino acid sequence without the substitution.
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