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公开(公告)号:US20200224186A1
公开(公告)日:2020-07-16
申请号:US16676253
申请日:2019-11-06
发明人: Neil KING , Wesley SUNDQUIST , Joerg VOTTELER , Yang HSIA , David BAKER , Jacob BALE , Marc LAJOIE , Gabriel BUTTERFIELD , Elizabeth GRAY , Daniel STETSON
IPC分类号: C12N9/88 , C07K14/00 , C07K14/435
摘要: The application discloses multimeric assemblies including multiple oligomeric substructures, where each oligomeric substructure includes multiple proteins that self-interact around at least one axis of rotational symmetry, where each protein includes one or more polypeptide-polypeptide interface (“O interface”); and one or more polypeptide domain that is capable of effecting membrane scission and release of an enveloped multimeric assembly from a cell by recruiting the ESCRT machinery to the site of budding by binding to one or more proteins in the eukaryotic ESCRT complex (“L domain”); and where the multimeric assembly includes one or more subunits comprising one or more polypeptide domain that is capable of interacting with a lipid bilayer (“M domain”), as well as membrane-enveloped versions of the multimeric assemblies.
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公开(公告)号:US20210340519A1
公开(公告)日:2021-11-04
申请号:US17336889
申请日:2021-06-02
发明人: Neil KING , Wesley SUNDQUIST , Joerg VOTTELER , Yang HSIA , David BAKER , Jacob BALE , Marc LAJOIE , Gabriel BUTTERFIELD , Elizabeth GRAY , Daniel STETSON
IPC分类号: C12N9/88 , C07K14/00 , C07K14/435
摘要: The application discloses multimeric assemblies including multiple oligomeric substructures, where each oligomeric substructure includes multiple proteins that self-interact around at least one axis of rotational symmetry, where each protein includes one or more polypeptide-polypeptide interface (“O interface”); and one or more polypeptide domain that is capable of effecting membrane scission and release of an enveloped multimeric assembly from a cell by recruiting the ESCRT machinery to the site of budding by binding to one or more proteins in the eukaryotic ESCRT complex (“L domain”); and where the multimeric assembly includes one or more subunits comprising one or more polypeptide domain that is capable of interacting with a lipid bilayer (“M domain”), as well as membrane-enveloped versions of the multimeric assemblies.
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公开(公告)号:US20180030429A1
公开(公告)日:2018-02-01
申请号:US15541201
申请日:2016-02-29
发明人: Neil KING , Wesley SUNDQUIST , Joerg VOTTELER , Yang HSIA , David BAKER , Jacob BALE , Marc LAJOIE , Gabriel BUTTERFIELD , Elizabeth GRAY , Daniel STETSON
IPC分类号: C12N9/88
CPC分类号: C12N9/88 , C07K14/00 , C07K14/435 , C07K2319/03 , C07K2319/06 , C07K2319/735 , C12Y401/02014
摘要: The application discloses multimeric assemblies including multiple oligomeric substructures, where each oligomeric substructure includes multiple proteins that self-interact around at least one axis of rotational symmetry, where each protein includes one or more polypeptide-polypeptide interface (“O interface”); and one or more polypeptide domain that is capable of effecting membrane scission and release of an enveloped multimeric assembly from a cell by recruiting the ESCRT machinery to the site of budding by binding to one or more proteins in the eukaryotic ESCRT complex (“L domain”); and where the multimeric assembly includes one or more subunits comprising one or more polypeptide domain that is capable of interacting with a lipid bilayer (“M domain”), as well as membrane-enveloped versions of the multimeric assemblies.
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公开(公告)号:US20210380641A1
公开(公告)日:2021-12-09
申请号:US16762565
申请日:2018-11-09
摘要: Synthetic nanostructures, polypeptides that are useful, for example, in making synthetic nanostructures, and methods for using synthetic nanostructures are disclosed herein.
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