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公开(公告)号:EP4141017A1
公开(公告)日:2023-03-01
申请号:EP21792412.5
申请日:2021-04-23
发明人: KANAI, Motomu , YAMATSUGU, Kenzo , TATSUMI, Toshifumi , KODAMA, Tatsuhiko , SUGIYAMA, Akira , TSUKAGOSHI, Masanobu , TOKUYAMA, Hidetoshi , SAKATA, Juri
摘要: It is an object of the present invention to provide a conjugate of a duocarmycin derivative and a biotin-modified dimer, which is useful for pretargeting methods. According to the present invention, a compound represented by the following formula (1) or formula (2) is provided:
wherein R 1 and R 2 each independently represent a hydrogen atom, a lower alkyl group, or a lower alkoxycarbonyl group; one of R 3 , R 4 , and R 5 represents -O-L 7 -(Xaa) m -L 6 -N 3 , and the remaining two each independently represent a hydrogen atom, a lower alkyl group, or a lower alkoxycarbonyl group; X represents a reactive group; L 6 and L 7 each independently represent a divalent linking group; Xaa represents an amino acid residue; m represents an integer of 2 to 10; and Me represents a methyl group.-
公开(公告)号:EP4382609A1
公开(公告)日:2024-06-12
申请号:EP22849576.8
申请日:2022-07-28
发明人: TANAKA, Toshiya , YAMASHITA, Takefumi , KODAMA, Tatsuhiko , KANAI, Motomu , YAMATSUGU, Kenzo , TATSUMI, Toshifumi , TAKAHASHI, Kazuki , SUGIYAMA, Akira , TSUKAGOSHI, Masanobu , CHANSLER, Michael , NAKAI, Masanori
IPC分类号: C12N15/62 , A61K31/409 , A61K38/16 , A61K47/66 , A61K49/00 , A61P35/00 , C07K14/195 , C07K16/30 , C07K19/00 , C12P21/02
CPC分类号: A61K31/409 , A61K38/16 , A61K47/66 , A61K49/00 , A61P35/00 , C07K14/195 , C07K16/30 , C07K19/00 , C12N15/62 , C12P21/02
摘要: It is an object of the present invention to provide a fusion protein of a molecule that recognizes cancer cells or the like and a mutant streptavidin, wherein the fusion protein is for use in the treatment or diagnosis of a cancer. According to the present invention, provided is A fusion protein, wherein an antigen-binding molecule having a molecular weight of 20,000 or less is bound, via a linker sequence, to the N-terminal side and/or C-terminal side of mutant streptavidin which comprises an amino acid sequence having the following mutations (1) to (6) with respect to the amino acid sequence of a core streptavidin as shown in SEQ ID NO: 17 provided that the C-terminal amino acid sequence consisting of Pro-Ser-Ala-Ala-Ser may be partially or entirely deleted, and has a decreased immunogenicity as compared with that of a wild-type streptavidin:
(1) a mutation in which the tyrosine residue at position 10 is substituted with serine or threonine;
(2) a mutation in which the tyrosine residue at position 71 is substituted with alanine or serine;
(3) a mutation in which the arginine residue at position 72 is substituted with lysine;
(4) a mutation in which the glutamic acid residue at position 89 is substituted with aspartic acid;
(5) a mutation in which the arginine residue at position 91 is substituted with lysine; and
(6) a mutation in which the glutamic acid residue at position 104 is substituted with glutamine or asparagine.
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