KRAS-specific capture agents, compositions, and methods of making and using

    公开(公告)号:US11414460B2

    公开(公告)日:2022-08-16

    申请号:US16933679

    申请日:2020-07-20

    发明人: James R. Heath

    IPC分类号: A61K38/00 C07K7/50

    摘要: Disclosed are compounds, compositions, and methods involving cyclic peptides that can bind to KRAS (G12D) oncogenic protein. For example, disclosed are cyclic peptides that selectively bind KRAS (G12D) oncogenic protein. Also disclosed are methods of inhibiting KRAS (G12D) oncogenic protein in a cancer cell expressing KRAS (G12D) oncogenic protein. In some forms, the method comprises incubating the cancer cell with any one or more of the disclosed cyclic peptides. In some forms, the method comprises bringing into contact the cancer cell with any one or more of the disclosed cyclic peptides.

    KRAS-Specific Capture Agents, Compositions, and Methods of Making and Using

    公开(公告)号:US20210032293A1

    公开(公告)日:2021-02-04

    申请号:US16933679

    申请日:2020-07-20

    发明人: James R. Heath

    IPC分类号: C07K7/50

    摘要: Disclosed are compounds, compositions, and methods involving cyclic peptides that can bind to KRAS (G12D) oncogenic protein. For example, disclosed are cyclic peptides that selectively bind KRAS (G12D) oncogenic protein. Also disclosed are methods of inhibiting KRAS (G12D) oncogenic protein in a cancer cell expressing KRAS (G12D) oncogenic protein. In some forms, the method comprises incubating the cancer cell with any one or more of the disclosed cyclic peptides. In some forms, the method comprises bringing into contact the cancer cell with any one or more of the disclosed cyclic peptides.

    KRAS-SPECIFIC CAPTURE AGENTS, COMPOSITIONS, AND METHODS OF MAKING AND USING

    公开(公告)号:US20220402971A1

    公开(公告)日:2022-12-22

    申请号:US17815805

    申请日:2022-07-28

    发明人: James R. Heath

    IPC分类号: C07K7/50

    摘要: Disclosed are compounds, compositions, and methods involving cyclic peptides that can bind to KRAS (G12D) oncogenic protein. For example, disclosed are cyclic peptides that selectively bind KRAS (G12D) oncogenic protein. Also disclosed are methods of inhibiting KRAS (G12D) oncogenic protein in a cancer cell expressing KRAS (G12D) oncogenic protein. In some forms, the method comprises incubating the cancer cell with any one or more of the disclosed cyclic peptides. In some forms, the method comprises bringing into contact the cancer cell with any one or more of the disclosed cyclic peptides.

    SARS-CoV-2 EPITOPE-TARGETED PEPTIDE IMMUNOSTIMULANTS

    公开(公告)号:US20210380640A1

    公开(公告)日:2021-12-09

    申请号:US17336276

    申请日:2021-06-01

    摘要: Disclosed are compounds, compositions, and methods relating to epitope-targeted immunostimulants (EPIs), which comprise a synthetic peptide ligand and an antibody-recruiting moiety. The peptide ligand binds an epitope on a target and the antibody-recruiting moiety recruits antibodies to the target when the EPI is bound to the epitope on the target. Also disclosed are compositions comprising any of the disclosed EPIs. Also disclosed are methods of stimulating an immune reaction to a microorganism or other pathogen in a subject where an EPI is administered to the subject. Also disclosed are methods of identifying the peptide ligand by using multi-omic analysis.

    EPITOPE-TARGETED PEPTIDE IMMUNOSTIMULANTS
    6.
    发明申请

    公开(公告)号:US20200323973A1

    公开(公告)日:2020-10-15

    申请号:US16841635

    申请日:2020-04-06

    摘要: Disclosed are compounds, compositions, and methods relating to epitope-targeted immunostimulants (EPIs), which comprise a synthetic peptide ligand and an antibody-recruiting moiety. The peptide ligand binds an epitope on a target and the antibody-recruiting moiety recruits antibodies to the target when the EPI is bound to the epitope on the target. Also disclosed are compositions comprising any of the disclosed EPIs. Also disclosed are methods of stimulating an immune reaction to a microorganism or other pathogen in a subject where an EPI is administered to the subject. Also disclosed are methods of identifying the peptide ligand by using multi-omic analysis.