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公开(公告)号:US12129465B2
公开(公告)日:2024-10-29
申请号:US17563271
申请日:2021-12-28
Inventor: Daniel Ellis , Neil King , Jesse Bloom , Tyler Starr , Allison Greaney
IPC: C07K14/165 , A61K39/215 , C12N15/11 , C12N15/64 , C12Q1/6811
CPC classification number: C12N15/11 , A61K39/215 , C07K14/165 , C12N15/64 , C12Q1/6811
Abstract: Provided herein are compositions and methods comprising mutated coronavirus “S” spike proteins or receptor binding domains thereof that have an increased expression level, yield and stability compared to its corresponding native or wild-type coronavirus spike protein under the same expression, culture or storage conditions. These mutated spike proteins can be used for generating a protein-based vaccine against one or more coronaviruses.
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公开(公告)号:US20240165218A1
公开(公告)日:2024-05-23
申请号:US18359154
申请日:2023-07-26
Applicant: University of Washington
Inventor: Neil King , David Baker , Lance Stewart , Brooke Fiala , Daniel Ellis , Lauren Carter , Rashmi Ravichandran , George Ueda , Jorge Fallas , Una Natterman
Abstract: The present disclosure provides nanostructures and nanostructure-based vaccines. Some nanostructures of the present disclosure display antigens capable of eliciting immune responses to infectious agents such as bacteria, viruses, and pathogens. Some vaccines of the present disclosure are useful for preventing or decreasing the severity of infection with an infectious agent, including. for example and without limitation, lyme disease, pertussis, herpes virus, orthomyxovirus, paramyxovirus, pneumovirus, filovirus. flavivirus, reovirus, retrovirus, meningococcus, or malaria. The antigens may be attached to the core of the nanostructure either non-covalently or covalently, including as a fusion protein or by other means disclosed herein. Multimeric antigens may optionally be displayed along a symmetry axis of the nanostructure. Also provided are proteins and nucleic acid molecules encoding such proteins. vaccine compositions, and methods of administration.
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公开(公告)号:US11485759B2
公开(公告)日:2022-11-01
申请号:US16427493
申请日:2019-05-31
Applicant: UNIVERSITY OF WASHINGTON
Inventor: David Baker , Jacob B. Bale , Neil P. King , William H. Sheffler , Daniel Ellis
IPC: C07K14/00
Abstract: Synthetic nanostructures, polypeptides that are useful, for example, in making synthetic nanostructures, and methods for using such synthetic nanostructures are disclosed herein.
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公开(公告)号:US09630994B2
公开(公告)日:2017-04-25
申请号:US14930792
申请日:2015-11-03
Applicant: UNIVERSITY OF WASHINGTON
Inventor: David Baker , Jacob B. Bale , Neil P. King , William H. Sheffler , Daniel Ellis
CPC classification number: C07K14/00
Abstract: Synthetic nanostructures, polypeptides that are useful, for example, in making synthetic nanostructures, and methods for using such synthetic nanostructures are disclosed herein.
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公开(公告)号:US10351603B2
公开(公告)日:2019-07-16
申请号:US15490351
申请日:2017-04-18
Applicant: UNIVERSITY OF WASHINGTON
Inventor: David Baker , Jacob B. Bale , Neil P. King , William H. Sheffler , Daniel Ellis
IPC: C07K14/00
Abstract: Synthetic nanostructures, polypeptides that are useful, for example, in making synthetic nanostructures, and methods for using such synthetic nanostructures are disclosed herein.
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公开(公告)号:US11771755B2
公开(公告)日:2023-10-03
申请号:US16971278
申请日:2019-02-28
Applicant: UNIVERSITY OF WASHINGTON
Inventor: Neil King , David Baker , Lance Stewart , Brooke Fiala , Daniel Ellis , Lauren Carter , Rashmi Ravichandran , George Ueda , Jorge Fallas , Una Nattermann
CPC classification number: A61K39/12 , C12N15/86 , B82Y5/00 , B82Y40/00 , C12N2710/16134 , C12N2710/16234 , C12N2760/00034
Abstract: Nanostructures and nanostructure-based vaccines that display antigens capable of eliciting immune responses to infectious agents such as bacteria, viruses, and pathogens are provided. Some vaccines are useful for preventing or decreasing the severity of infection with an infectious agent, including, for example and without limitation, lyme disease, pertussis, herpes virus, orthomyxovirus, paramyxovirus, pneumovirus, filovirus, flavivirus, reovirus, retrovirus, meningococcus, or malaria. The antigens may be attached to the core of the nanostructure either non-covalently or covalently, including as a fusion protein or by other means. Multimeric antigens may optionally be displayed along a symmetry axis of the nanostructure. Also provided are proteins and nucleic acid molecules encoding such proteins, vaccine compositions, and methods of administration.
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