Structure of SARS-CoV-2 Spike Glycoprotein for Therapeutic and Preventive Target
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Soohyun Kim | Chang-Seon Song | Jaewoo Hong | Suyoung Bae | H. Jhun | S. Yeom | Youngmin Lee | Yeo-Ok Choi | Afeisha S Taitt
[1] Elisabeth Mahase. Covid-19: Novavax vaccine efficacy is 86% against UK variant and 60% against South African variant , 2021, BMJ.
[2] Vineet D. Menachery,et al. Neutralization of SARS-CoV-2 spike 69/70 deletion, E484K, and N501Y variants by BNT162b2 vaccine-elicited sera , 2021, bioRxiv.
[3] D. Hui,et al. Introduction of the South African SARS-CoV-2 variant 501Y.V2 into the UK , 2021, Journal of Infection.
[4] G. Gao,et al. Viral targets for vaccines against COVID-19 , 2020, Nature reviews. Immunology.
[5] Amanda M Li,et al. CRISPR-Cas9 Gene Editing for Sickle Cell Disease and β-Thalassemia. , 2020, The New England journal of medicine.
[6] Shiu-Wan Chan. Current and Future Direct-Acting Antivirals Against COVID-19 , 2020, Frontiers in Microbiology.
[7] H. Woo,et al. Mutations in the SARS-CoV-2 spike RBD are responsible for stronger ACE2 binding and poor anti-SARS-CoV mAbs cross-neutralization , 2020, Computational and Structural Biotechnology Journal.
[8] Elisabeth Mahase. Covid-19: FDA authorises neutralising antibody bamlanivimab for non-admitted patients , 2020, BMJ.
[9] Ye Xiang,et al. Spike Glycoprotein-Mediated Entry of SARS Coronaviruses , 2020, Viruses.
[10] V. Thiel,et al. Coronavirus biology and replication: implications for SARS-CoV-2 , 2020, Nature Reviews Microbiology.
[11] Vineet D. Menachery,et al. Spike mutation D614G alters SARS-CoV-2 fitness , 2020, Nature.
[12] E. Chan,et al. The Progression of SARS Coronavirus 2 (SARS-CoV2): Mutation in the Receptor Binding Domain of Spike Gene , 2020, Immune network.
[13] D. Yokoe,et al. Treatment of immunocompromised COVID‐19 patients with convalescent plasma , 2020, Transplant infectious disease : an official journal of the Transplantation Society.
[14] P. Gallian,et al. Convalescent plasma therapy for B-cell–depleted patients with protracted COVID-19 , 2020, Blood.
[15] S. Kent,et al. Antibody-dependent enhancement and SARS-CoV-2 vaccines and therapies , 2020, Nature Microbiology.
[16] M. Halloran,et al. Zika virus infection enhances future risk of severe dengue disease , 2020, Science.
[17] A. Pain,et al. A genetic barcode of SARS-CoV-2 for monitoring global distribution of different clades during the COVID-19 pandemic , 2020, International Journal of Infectious Diseases.
[18] J. Bloom,et al. Neutralizing antibodies correlate with protection from SARS-CoV-2 in humans during a fishery vessel outbreak with high attack rate , 2020, medRxiv.
[19] N. Sofat,et al. Immunomodulatory Drugs in the Management of SARS-CoV-2 , 2020, Frontiers in Immunology.
[20] D. Lauffenburger,et al. Single-Shot Ad26 Vaccine Protects Against SARS-CoV-2 in Rhesus Macaques , 2020, Nature.
[21] G. Gao,et al. Single-Cell Sequencing of Peripheral Mononuclear Cells Reveals Distinct Immune Response Landscapes of COVID-19 and Influenza Patients , 2020, Immunity.
[22] Sasikanth Manne,et al. Deep immune profiling of COVID-19 patients reveals distinct immunotypes with therapeutic implications , 2020, Science.
[23] W. Cao,et al. High-Dose Intravenous Immunoglobulins in the Treatment of Severe Acute Viral Pneumonia: The Known Mechanisms and Clinical Effects , 2020, Frontiers in Immunology.
[24] R. W. Janes,et al. Identification of a druggable binding pocket in the spike protein reveals a key site for existing drugs potentially capable of combating Covid-19 infectivity , 2020, BMC Molecular and Cell Biology.
[25] Morten Nielsen,et al. Robust T Cell Immunity in Convalescent Individuals with Asymptomatic or Mild COVID-19 , 2020, Cell.
[26] S. Rowland-Jones,et al. Tracking Changes in SARS-CoV-2 Spike: Evidence that D614G Increases Infectivity of the COVID-19 Virus , 2020, Cell.
[27] F. Iacovelli,et al. Targeting the SARS-CoV-2 spike glycoprotein prefusion conformation: virtual screening and molecular dynamics simulations applied to the identification of potential fusion inhibitors , 2020, Virus Research.
[28] R. Welsh,et al. Studies in humanized mice and convalescent humans yield a SARS-CoV-2 antibody cocktail , 2020, Science.
[29] I. Tizard. Vaccination against coronaviruses in domestic animals , 2020, Vaccine.
[30] Rongchang Chen,et al. Generation of a Broadly Useful Model for COVID-19 Pathogenesis, Vaccination, and Treatment , 2020, Cell.
[31] G. Gao,et al. Development of an Inactivated Vaccine Candidate, BBIBP-CorV, with Potent Protection against SARS-CoV-2 , 2020, Cell.
[32] M. Nussenzweig,et al. Structures of human antibodies bound to SARS-CoV-2 spike reveal common epitopes and recurrent features of antibodies , 2020, bioRxiv.
[33] Linqi Zhang,et al. Human neutralizing antibodies elicited by SARS-CoV-2 infection , 2020, Nature.
[34] Andrew S. Paluch,et al. Repurposing approved drugs as inhibitors of SARS-CoV-2 S-protein from molecular modeling and virtual screening , 2020, Journal of biomolecular structure & dynamics.
[35] L. Guddat,et al. Structural Basis for RNA Replication by the SARS-CoV-2 Polymerase , 2020, Cell.
[36] R. Baric,et al. DNA vaccine protection against SARS-CoV-2 in rhesus macaques , 2020, Science.
[37] X. Xie,et al. Potent Neutralizing Antibodies against SARS-CoV-2 Identified by High-Throughput Single-Cell Sequencing of Convalescent Patients’ B Cells , 2020, Cell.
[38] Ogun Adebali,et al. Phylogenetic analysis of SARS-CoV-2 genomes in Turkey , 2020, bioRxiv.
[39] M. V. van Breemen,et al. Potent neutralizing antibodies from COVID-19 patients define multiple targets of vulnerability , 2020, Science.
[40] Lu Lu,et al. Identification of Human Single-Domain Antibodies against SARS-CoV-2 , 2020, Cell Host & Microbe.
[41] F. Gao,et al. A noncompeting pair of human neutralizing antibodies block COVID-19 virus binding to its receptor ACE2 , 2020, Science.
[42] Fang Li,et al. Cell entry mechanisms of SARS-CoV-2 , 2020, Proceedings of the National Academy of Sciences.
[43] Xiangxi Wang,et al. Development of an inactivated vaccine candidate for SARS-CoV-2 , 2020, Science.
[44] Xifeng Lu,et al. In silico design of antiviral peptides targeting the spike protein of SARS-CoV-2 , 2020, Peptides.
[45] Sumra Wajid Abbasi,et al. Stilbene-based natural compounds as promising drug candidates against COVID-19 , 2020, Journal of biomolecular structure & dynamics.
[46] N. Carragher,et al. Highly Conserved Homotrimer Cavity Formed by the SARS-CoV-2 Spike Glycoprotein: A Novel Binding Site , 2020, Journal of clinical medicine.
[47] S. Zhang,et al. Neutralization of SARS-CoV-2 spike pseudotyped virus by recombinant ACE2-Ig , 2020, Nature Communications.
[48] Martin Stahl,et al. Inhibition of SARS-CoV-2 Infections in Engineered Human Tissues Using Clinical-Grade Soluble Human ACE2 , 2020, Cell.
[49] M. Bianchini,et al. A possible strategy to fight COVID-19: Interfering with spike glycoprotein trimerization , 2020, Biochemical and Biophysical Research Communications.
[50] Wayne T. Nicholson,et al. Deployment of convalescent plasma for the prevention and treatment of COVID-19. , 2020, The Journal of clinical investigation.
[51] K. Yuen,et al. Structural and Functional Basis of SARS-CoV-2 Entry by Using Human ACE2 , 2020, Cell.
[52] Linqi Zhang,et al. Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor , 2020, Nature.
[53] Yuxian He,et al. Design of Potent Membrane Fusion Inhibitors against SARS-CoV-2, an Emerging Coronavirus with High Fusogenic Activity , 2020, Journal of Virology.
[54] Yan Liu,et al. Characterization of spike glycoprotein of SARS-CoV-2 on virus entry and its immune cross-reactivity with SARS-CoV , 2020, Nature Communications.
[55] Jing Yuan,et al. Treatment of 5 Critically Ill Patients With COVID-19 With Convalescent Plasma. , 2020, JAMA.
[56] K. Shi,et al. Structural basis of receptor recognition by SARS-CoV-2 , 2020, Nature.
[57] G. Herrler,et al. SARS-CoV-2 Cell Entry Depends on ACE2 and TMPRSS2 and Is Blocked by a Clinically Proven Protease Inhibitor , 2020, Cell.
[58] Qiang Zhou,et al. Structural basis for the recognition of SARS-CoV-2 by full-length human ACE2 , 2020, Science.
[59] Arthur S Slutsky,et al. Angiotensin-converting enzyme 2 (ACE2) as a SARS-CoV-2 receptor: molecular mechanisms and potential therapeutic target , 2020, Intensive Care Medicine.
[60] Young-Jun Park,et al. Structure, Function, and Antigenicity of the SARS-CoV-2 Spike Glycoprotein , 2020, Cell.
[61] B. Graham,et al. Cryo-EM structure of the 2019-nCoV spike in the prefusion conformation , 2020, Science.
[62] Lu Lu,et al. Fusion mechanism of 2019-nCoV and fusion inhibitors targeting HR1 domain in spike protein , 2020, Cellular & Molecular Immunology.
[63] Kai Zhao,et al. A pneumonia outbreak associated with a new coronavirus of probable bat origin , 2020, Nature.
[64] E. Holmes,et al. Genomic characterisation and epidemiology of 2019 novel coronavirus: implications for virus origins and receptor binding , 2020, The Lancet.
[65] Y. Hu,et al. Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China , 2020, The Lancet.
[66] Fang Li,et al. Molecular Mechanism for Antibody-Dependent Enhancement of Coronavirus Entry , 2019, Journal of Virology.
[67] Lu Lu,et al. IgG Fc-binding motif-conjugated HIV-1 fusion inhibitor exhibits improved potency and in vivo half-life: Potential application in combination with broad neutralizing antibodies , 2019, PLoS pathogens.
[68] H. Xing,et al. Long-Acting HIV-1 Fusion Inhibitory Peptides and their Mechanisms of Action , 2019, Viruses.
[69] T. Takano,et al. Pathogenesis of oral type I feline infectious peritonitis virus (FIPV) infection: Antibody-dependent enhancement infection of cats with type I FIPV via the oral route , 2019, The Journal of veterinary medical science.
[70] Lu Lu,et al. A pan-coronavirus fusion inhibitor targeting the HR1 domain of human coronavirus spike , 2019, Science Advances.
[71] Q. Wang,et al. A Peptide-Based HIV-1 Fusion Inhibitor with Two Tail-Anchors and Palmitic Acid Exhibits Substantially Improved In Vitro and Ex Vivo Anti-HIV-1 Activity and Prolonged In Vivo Half-Life , 2019, Molecules.
[72] Chuan Qin,et al. Anti-spike IgG causes severe acute lung injury by skewing macrophage responses during acute SARS-CoV infection. , 2019, JCI insight.
[73] Xinquan Wang,et al. Cryo-EM structure of the SARS coronavirus spike glycoprotein in complex with its host cell receptor ACE2 , 2018, PLoS pathogens.
[74] M. Porotto,et al. Fusion Inhibitory Lipopeptides Engineered for Prophylaxis of Nipah Virus in Primates , 2018, The Journal of infectious diseases.
[75] F. Luo,et al. Evaluation of Antibody-Dependent Enhancement of SARS-CoV Infection in Rhesus Macaques Immunized with an Inactivated SARS-CoV Vaccine , 2018, Virologica Sinica.
[76] K. Stiasny,et al. The bright and the dark side of human antibody responses to flaviviruses: lessons for vaccine design , 2017, EMBO reports.
[77] C. Heinis,et al. Acylated heptapeptide binds albumin with high affinity and application as tag furnishes long-acting peptides , 2017, Nature Communications.
[78] Yi Shi,et al. Cryo-EM structures of MERS-CoV and SARS-CoV spike glycoproteins reveal the dynamic receptor binding domains , 2017, Nature Communications.
[79] Soohyun Kim,et al. Intracellular interleukin (IL)-1 family cytokine processing enzyme , 2016, Archives of pharmacal research.
[80] Yong-Sung Kim,et al. Proinsulin Shares a Motif with Interleukin-1α (IL-1α) and Induces Inflammatory Cytokine via Interleukin-1 Receptor 1* , 2016, The Journal of Biological Chemistry.
[81] Jing Xie,et al. Immunodominant SARS Coronavirus Epitopes in Humans Elicited both Enhancing and Neutralizing Effects on Infection in Non-human Primates , 2016, ACS infectious diseases.
[82] G. Gao,et al. Glycosylated enfuvirtide: a long-lasting glycopeptide with potent anti-HIV activity. , 2015, Journal of medicinal chemistry.
[83] G. Whittaker,et al. Host cell entry of Middle East respiratory syndrome coronavirus after two-step, furin-mediated activation of the spike protein , 2014, Proceedings of the National Academy of Sciences.
[84] Fu-Tong Liu,et al. Antibody-dependent SARS coronavirus infection is mediated by antibodies against spike proteins , 2014, Biochemical and Biophysical Research Communications.
[85] R. Baric,et al. Rapid generation of a mouse model for Middle East respiratory syndrome , 2014, Proceedings of the National Academy of Sciences.
[86] M. Porotto,et al. Prevention of Measles Virus Infection by Intranasal Delivery of Fusion Inhibitor Peptides , 2014, Journal of Virology.
[87] C. Dinarello,et al. The Interleukin-1α Precursor is Biologically Active and is Likely a Key Alarmin in the IL-1 Family of Cytokines , 2013, Front. Immunol..
[88] R. Couch,et al. Immunization with SARS Coronavirus Vaccines Leads to Pulmonary Immunopathology on Challenge with the SARS Virus , 2012, PloS one.
[89] Lisa E. Gralinski,et al. A Double-Inactivated Severe Acute Respiratory Syndrome Coronavirus Vaccine Provides Incomplete Protection in Mice and Induces Increased Eosinophilic Proinflammatory Pulmonary Response upon Challenge , 2011, Journal of Virology.
[90] J. Peiris,et al. Anti-Severe Acute Respiratory Syndrome Coronavirus Spike Antibodies Trigger Infection of Human Immune Cells via a pH- and Cysteine Protease-Independent FcγR Pathway , 2011, Journal of Virology.
[91] S. Munro,et al. A Comprehensive Comparison of Transmembrane Domains Reveals Organelle-Specific Properties , 2010, Cell.
[92] Jincun Zhao,et al. T Cell Responses Are Required for Protection from Clinical Disease and for Virus Clearance in Severe Acute Respiratory Syndrome Coronavirus-Infected Mice , 2010, Journal of Virology.
[93] Christopher D. Paddock,et al. Cellular Immune Responses to Severe Acute Respiratory Syndrome Coronavirus (SARS-CoV) Infection in Senescent BALB/c Mice: CD4+ T Cells Are Important in Control of SARS-CoV Infection , 2009, Journal of Virology.
[94] G. Whittaker,et al. Activation of the SARS coronavirus spike protein via sequential proteolytic cleavage at two distinct sites , 2009, Proceedings of the National Academy of Sciences.
[95] T. Takano,et al. Antibody-dependent enhancement occurs upon re-infection with the identical serotype virus in feline infectious peritonitis virus infection. , 2008, The Journal of veterinary medical science.
[96] S. Inoue,et al. Prior Immunization with Severe Acute Respiratory Syndrome (SARS)-Associated Coronavirus (SARS-CoV) Nucleocapsid Protein Causes Severe Pneumonia in Mice Infected with SARS-CoV1 , 2008, The Journal of Immunology.
[97] S. Keidar,et al. ACE2 of the heart: From angiotensin I to angiotensin (1-7). , 2007, Cardiovascular research.
[98] R. Johnston,et al. Vaccine Efficacy in Senescent Mice Challenged with Recombinant SARS-CoV Bearing Epidemic and Zoonotic Spike Variants , 2006, PLoS medicine.
[99] M. Peiris,et al. Antibodies against trimeric S glycoprotein protect hamsters against SARS-CoV challenge despite their capacity to mediate FcγRII-dependent entry into B cells in vitro , 2006, Vaccine.
[100] A. Bernkop‐Schnürch,et al. Strategies to improve plasma half life time of peptide and protein drugs , 2006, Amino Acids.
[101] J. Ziebuhr,et al. Nidovirales: Evolving the largest RNA virus genome , 2006, Virus Research.
[102] S. Harrison,et al. Structure of SARS Coronavirus Spike Receptor-Binding Domain Complexed with Receptor , 2005, Science.
[103] Y. Zhang,et al. Immunogenicity and protective efficacy in monkeys of purified inactivated Vero-cell SARS vaccine , 2005, Vaccine.
[104] Chengsheng Zhang,et al. Receptor and viral determinants of SARS-coronavirus adaptation to human ACE2 , 2005, The EMBO journal.
[105] Wenhui Li,et al. A 193-Amino Acid Fragment of the SARS Coronavirus S Protein Efficiently Binds Angiotensin-converting Enzyme 2* , 2004, Journal of Biological Chemistry.
[106] H. Vennema,et al. Early death after feline infectious peritonitis virus challenge due to recombinant vaccinia virus immunization , 1990, Journal of virology.
[107] G. Blobel,et al. Translocation of proteins across the endoplasmic reticulum. I. Signal recognition protein (SRP) binds to in-vitro-assembled polysomes synthesizing secretory protein , 1981, The Journal of cell biology.
[108] A. Allison,et al. Dengue viruses and mononuclear phagocytes. II. Identity of blood and tissue leukocytes supporting in vitro infection , 1977, The Journal of experimental medicine.
[109] SB Halstead,et al. Dengue viruses and mononuclear phagocytes. I. Infection enhancement by non-neutralizing antibody , 1977, The Journal of experimental medicine.
[110] B. Dobberstein,et al. Transfer of proteins across membranes. I. Presence of proteolytically processed and unprocessed nascent immunoglobulin light chains on membrane-bound ribosomes of murine myeloma , 1975, The Journal of cell biology.
[111] C. E.. WHO Coronavirus Disease (COVID-19) Dashboard , 2020 .
[112] J. Luban. SARS-CoV-2 , 2020 .
[113] T. Hohdatsu,et al. A study on the mechanism of antibody-dependent enhancement of feline infectious peritonitis virus infection in feline macrophages by monoclonal antibodies , 2005, Archives of Virology.