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公开(公告)号:US20240366783A1
公开(公告)日:2024-11-07
申请号:US18666145
申请日:2024-05-16
Applicant: AJINOMOTO CO., INC.
Inventor: Kei YAMADA , Yutaka MATSUDA , Tomohiro FUJII , Natsuki SHIKIDA , Reiko YUJI , Kazutaka SHIMBO , Yuji ITO
Abstract: The present invention provides a technique enabling modification of a soluble protein and in particular regioselective modification of a soluble protein. More specifically, the present invention provides a compound having an affinity substance to a soluble protein, a cleavable portion, and a reactive group represented by the following Formula (I): A-L-B-R (I) wherein A is an affinity substance to a soluble protein; L is a cleavable linker which is a divalent group comprising a cleavable portion; B is (a) a divalent group comprising a bioorthogonal functional group or (b) a divalent group comprising no bioorthogonal functional group; and R is a reactive group to the soluble protein; or a salt thereof.
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公开(公告)号:US20210139549A1
公开(公告)日:2021-05-13
申请号:US17119786
申请日:2020-12-11
Applicant: AJINOMOTO CO., INC.
Inventor: Kei YAMADA , Tomohiro FUJII , Natsuki SHIKIDA , Kazutaka SHIMBO
Abstract: Compounds having an affinity substance to an antibody, a cleavable portion, and a reactive group, represented by the following Formula (I): A-L-B-R (I) wherein A is the affinity substance an antibody, L is a cleavable linker which is a divalent group comprising the cleavable portion, B is (a) a divalent group comprising a bioorthogonal functional group or (b) a divalent group comprising no bioorthogonal functional group, and R is the reactive group to the antibody, in which the affinity substance to an antibody is a certain peptide, or a salt thereof are useful for the modification of an antibody, particularly the regioselective modification of an antibody.
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公开(公告)号:US20240058473A1
公开(公告)日:2024-02-22
申请号:US18467134
申请日:2023-09-14
Applicant: Ajinomoto Co., Inc.
Inventor: Kei YAMADA , Yutaka MATSUDA , Ippei INOUE , Natsuki SHIKIDA , Kazutaka SHIMBO
CPC classification number: A61K47/6949 , A61K47/6835 , A61K47/6889
Abstract: The present invention provides a highly controlled complex comprising an antibody and ferritin particles. More specifically, the present invention provides the inventions of a complex or salt thereof comprising (A) one IgG antibody and (B) two human ferritin particles comprising one or more human ferritin H chains linked thereto; and methods for producing the same.
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公开(公告)号:US20230279063A1
公开(公告)日:2023-09-07
申请号:US18062906
申请日:2022-12-07
Applicant: Ajinomoto Co., Inc.
Inventor: Kei YAMADA , Ippei INOUE , Natsuki SHIKIDA , Kazutaka SHIMBO
Abstract: Controlling the number of modifying groups introduced into a surface of ferritin affords a modified ferritin containing a human ferritin H chain, in which the human ferritin H chain contains a modifying group that is covalently bonded specifically to a cysteine residue at position 91 and/or position 103 according to a reference position of a natural human ferritin H chain.
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公开(公告)号:US20210300972A1
公开(公告)日:2021-09-30
申请号:US17241585
申请日:2021-04-27
Applicant: Ajinomoto Co., Inc.
Inventor: Kei YAMADA , Yoshihiko MATSUDA , Kazutoshi TAKAHASHI , Natsuki SHIKIDA , Kazutaka SHIMBO , Hayato NAGANO
Abstract: Compounds having an affinity substance to an antibody, a cleavable portion, and a reactive group, or a salt thereof, are represented by the following Formula (I): A-L-B—R (I) wherein A is an affinity substance to an antibody, L is a cleavable linker that is a divalent group comprising a cleavable portion, B is (a) a divalent group comprising a bioorthogonal functional group or (b) a divalent group comprising no bioorthogonal functional group, and R is a reactive group to the antibody, wherein the affinity substance to an antibody is a polypeptide comprising a glutamine residue (Q) at an N-terminal.
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公开(公告)号:US20210139541A1
公开(公告)日:2021-05-13
申请号:US17119495
申请日:2020-12-11
Applicant: Ajinomoto Co., Inc.
Inventor: Yutaka MATSUDA , Noriko HATADA , Kei YAMADA , Natsuki SHIKIDA , Kazutaka SHIMBO , Tomohiro FUJII , Shigeo HIRASAWA
Abstract: Compounds having an affinity substance to an antibody and a bioorthogonal functional group, represented by the following Formula (I): A-L-E-B (I) wherein A is an affinity substance to an antibody, L is a divalent group comprising a leaving group, E is a divalent group comprising an electrophilic group (i) coupled with the leaving group and (ii) having ability to react with a nucleophilic group in the antibody, B is a bioorthogonal functional group, and the leaving group has ability to be cleaved and eliminated from E by a reaction between the nucleophilic group and the electrophilic group, or a salt thereof, and the like are useful for labelling antibodies.
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