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Basic Characteristics of Mutations
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Mutation Site
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S494R |
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Mutation Site Sentence
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TABLE |
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Mutation Level
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Amino acid level |
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Mutation Type
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Nonsynonymous substitution |
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Gene/Protein/Region
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S |
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Standardized Encoding Gene
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S
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Genotype/Subtype
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B.1.1.7 |
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Viral Reference
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-
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Functional Impact and Mechanisms
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Disease
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-
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Immune
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- |
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Target Gene
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-
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Clinical and Epidemiological Correlations
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Clinical Information
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- |
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Treatment
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- |
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Location
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- |
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Literature Information
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PMID
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35568025
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Title
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LY-CoV1404 (bebtelovimab) potently neutralizes SARS-CoV-2 variants
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Author
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Westendorf K,Zentelis S,Wang L,Foster D,Vaillancourt P,Wiggin M,Lovett E,van der Lee R,Hendle J,Pustilnik A,Sauder JM,Kraft L,Hwang Y,Siegel RW,Chen J,Heinz BA,Higgs RE,Kallewaard NL,Jepson K,Goya R,Smith MA,Collins DW,Pellacani D,Xiang P,de Puyraimond V,Ricicova M,Devorkin L,Pritchard C,O'Neill A,Dalal K,Panwar P,Dhupar H,Garces FA,Cohen CA,Dye JM,Huie KE,Badger CV,Kobasa D,Audet J,Freitas JJ,Hassanali S,Hughes I,Munoz L,Palma HC,Ramamurthy B,Cross RW,Geisbert TW,Menachery V,Lokugamage K,Borisevich V,Lanz I,Anderson L,Sipahimalani P,Corbett KS,Yang ES,Zhang Y,Shi W,Zhou T,Choe M,Misasi J,Kwong PD,Sullivan NJ,Graham BS,Fernandez TL,Hansen CL,Falconer E,Mascola JR,Jones BE,Barnhart BC
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Journal
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Cell reports
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Journal Info
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2022 May 17;39(7):110812
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Abstract
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Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2)-neutralizing monoclonal antibodies (mAbs) can reduce the risk of hospitalization from coronavirus disease 2019 (COVID-19) when administered early. However, SARS-CoV-2 variants of concern (VOCs) have negatively affected therapeutic use of some authorized mAbs. Using a high-throughput B cell screening pipeline, we isolated LY-CoV1404 (bebtelovimab), a highly potent SARS-CoV-2 spike glycoprotein receptor binding domain (RBD)-specific antibody. LY-CoV1404 potently neutralizes authentic SARS-CoV-2, B.1.1.7, B.1.351, and B.1.617.2. In pseudovirus neutralization studies, LY-CoV1404 potently neutralizes variants, including B.1.1.7, B.1.351, B.1.617.2, B.1.427/B.1.429, P.1, B.1.526, B.1.1.529, and the BA.2 subvariant. Structural analysis reveals that the contact residues of the LY-CoV1404 epitope are highly conserved, except for N439 and N501. The binding and neutralizing activity of LY-CoV1404 is unaffected by the most common mutations at these positions (N439K and N501Y). The broad and potent neutralization activity and the relatively conserved epitope suggest that LY-CoV1404 has the potential to be an effective therapeutic agent to treat all known variants.
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Sequence Data
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-
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