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10.1002/advs.202102181

http://scihub22266oqcxt.onion/10.1002/advs.202102181
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suck abstract from ncbi


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pmid34716683      Adv+Sci+(Weinh) 2022 ; 9 (1): e2102181
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  • Neutralizing Antibodies to SARS-CoV-2 Selected from a Human Antibody Library Constructed Decades Ago #MMPMID34716683
  • Qiang M; Ma P; Li Y; Liu H; Harding A; Min C; Wang F; Liu L; Yuan M; Ji Q; Tao P; Shi X; Li Z; Li T; Wang X; Zhang Y; Wu NC; Lee CD; Zhu X; Gilbert-Jaramillo J; Zhang C; Saxena A; Huang X; Wang H; James W; Dwek RA; Wilson IA; Yang G; Lerner RA
  • Adv Sci (Weinh) 2022[Jan]; 9 (1): e2102181 PMID34716683show ga
  • Combinatorial antibody libraries not only effectively reduce antibody discovery to a numbers game, but enable documentation of the history of antibody responses in an individual. The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) pandemic has prompted a wider application of this technology to meet the public health challenge of pandemic threats in the modern era. Herein, a combinatorial human antibody library constructed 20 years before the coronavirus disease 2019 (COVID-19) pandemic is used to discover three highly potent antibodies that selectively bind SARS-CoV-2 spike protein and neutralize authentic SARS-CoV-2 virus. Compared to neutralizing antibodies from COVID-19 patients with generally low somatic hypermutation (SHM), these three antibodies contain over 13-22 SHMs, many of which are involved in specific interactions in their crystal structures with SARS-CoV-2 spike receptor binding domain. The identification of these somatically mutated antibodies in a pre-pandemic library raises intriguing questions about the origin and evolution of these antibodies with respect to their reactivity with SARS-CoV-2.
  • |Angiotensin-Converting Enzyme 2/genetics/*metabolism[MESH]
  • |Animals[MESH]
  • |Antibodies, Neutralizing/genetics/*immunology/metabolism/pharmacology[MESH]
  • |Antibodies, Viral/immunology[MESH]
  • |Binding Sites[MESH]
  • |Binding, Competitive[MESH]
  • |Cell Surface Display Techniques[MESH]
  • |Chlorocebus aethiops[MESH]
  • |HEK293 Cells[MESH]
  • |Humans[MESH]
  • |Peptide Library[MESH]
  • |SARS-CoV-2/drug effects/*immunology[MESH]
  • |Somatic Hypermutation, Immunoglobulin[MESH]
  • |Spike Glycoprotein, Coronavirus/genetics/immunology/*metabolism[MESH]


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