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公开(公告)号:US20190248872A1
公开(公告)日:2019-08-15
申请号:US16254114
申请日:2019-01-22
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Ray Camphausen , Amna Saeed-Kothe , Jonathan Davis , Tracy S. Mitchell
IPC: C07K14/78 , C07K16/28 , C07K16/40 , C07K16/46 , C07K7/08 , C07K7/06 , G01N33/573 , C07K16/24 , C07K14/47
CPC classification number: C07K14/78 , A61K38/00 , C07K7/06 , C07K7/08 , C07K14/47 , C07K16/244 , C07K16/2863 , C07K16/40 , C07K16/46 , C07K2317/92 , C07K2317/94 , C07K2318/20 , C07K2319/30 , G01N33/573 , G01N2333/948
Abstract: The application provides Fc fusion proteins having novel arrangements. In one embodiment, the application provides Fc fusion proteins comprising a 10Fn3 domain. In another embodiment, the application provides Fc fusion proteins comprising linkers derived from the naturally occurring C-terminal tail regions of membrane bound or secretory immunoglobulins.
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公开(公告)号:US10214579B2
公开(公告)日:2019-02-26
申请号:US15257189
申请日:2016-09-06
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Ray Camphausen , Amna Saeed-Kothe , Jonathan Davis , Tracy S. Mitchell
IPC: C07K14/78 , C07K14/47 , C07K7/06 , C07K7/08 , A61K38/00 , C07K16/24 , C07K16/28 , C07K16/40 , C07K16/46 , G01N33/573
Abstract: The application provides Fc fusion proteins having novel arrangements. In one embodiment, the application provides Fc fusion proteins comprising a 10F3 domain. In another embodiment, the application provides Fc fusion proteins comprising linkers derived from the naturally occurring C-terminal tail regions of membrane bound or secretory immunoglobulins.
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公开(公告)号:US09416170B2
公开(公告)日:2016-08-16
申请号:US13757664
申请日:2013-02-01
Applicant: BRISTOL-MYERS SQUIBB COMPANY
Inventor: Jonathan Davis , Dasa Lipovsek , Ray Camphausen
CPC classification number: C07K14/78 , A61K38/00 , C07K14/47 , C07K16/241 , C07K16/244 , C07K16/28 , C07K16/2833 , C07K16/2857 , C07K2317/92 , C07K2318/20 , C12N15/1062 , C40B40/10 , G01N33/68 , G01N33/6887
Abstract: Fibronectin type III (10Fn3) binding domains having novel designs that are associated with reduced immunogenicity are provided. The application describes alternative 10Fn3 binding domains in which certain immunogenic regions are not modified when producing a binder in order to maintain recognition as a self antigen by the host organism. The application also describes 10Fn3 binding domains in which HLA anchor regions have been destroyed thereby reducing the immunogenic contribution of the adjoining region. Also provided are 10Fn3 domains having novel combinations of modified regions that can bind to a desired target with high affinity.
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