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      Proteomics-based Insights into the SARS-CoV-2 Mediated COVID-19 Pandemic: A Review of the First Year of Research

      review-article
      ,
      Molecular & Cellular Proteomics : MCP
      THE AUTHORS. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology.
      3CLpro, (3C-like protease), ACE2, (angiotensin-converting enzyme 2), ADP, (adenosine diphosphate), BioGRID, (Biological General Repository for Interaction Datasets), COVID-19, (Coronavirus Disease 2019), CP, (cytoplasm), CPTAC, (Clinical Proteomic Tumor Analysis Consortium), DDA, (data-dependent acquisition), deamid, (deamidation), DIA, (data-independent acquisition), E, (envelope protein), EMBL-EBI, (European Molecular Biology Laboratory, European Bioinformatics Institute), EN, (endosome), ER, (endoplasmic reticulum), ERGIC, (endoplasmic reticulum golgi intermediate compartment), ERM, (endoplasmic reticulum membrane), esp, (especially), Fe-NTA, (ferric nitrilotriacetate), FP, (fusion peptide), GISAID, (Global Initiative on Sharing Avian Influenza Data), gRNA, (genomic RNA), HCD, (higher-energy collisional dissociation), HR1, (heptad repeat 1), HR2, (heptad repeat 2), HS, (heparan sulfate), LC-MS, (liquid chromatography, mass spectrometry), LLOD, (lower limit of detection), LY, (lysosome), M, (membrane protein), MAVS, (mitochondrial antiviral signaling), mePROD, (multiplexed enhanced protein dynamics), MOI, (multiplicity of infection), Mpro, (main protease), MT, (mitochondria), N, (nucleocapsid protein), NCBI, (National Center for Biotechnology Information), NM, (nuclear membrane), NMD, (nonsense mediated decay), NO, (nucleolus), nsp, (nonstructural protein), NU, (nucleus), ORF, (open reading frame), oxid, (oxidation), PBMC, (peripheral blood mononuclear cell), PCR, (polymerase chain reaction), PLpro, (papain-like protease), PM, (plasma membrane), PN, (perinuclear), PPI, (protein-protein interaction), PRM, (parallel reaction monitoring), PTM, (post-translational modification), qPCR, (quantitative polymerase chain reaction), RBD, (receptor binding domain), RNP, (ribonucleoprotein), RPLC, (reversed phase liquid chromatography), S, (spike or surface glycoprotein), SARS, (Severe Acute Respiratory Syndrome), SARS-CoV-1, (Severe Acute Respiratory Syndrome Coronavirus 1), SARS-CoV-2, (Severe Acute Respiratory Syndrome Coronavirus 2), sgRNA, (subgenomic RNA), SILAC, (Stable Isotope Labeling by Amino acids in Cell culture), ss-RNA, (single-stranded RNA), TMT, (tandem mass tag)

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          Abstract

          In late 2019, a virus subsequently named Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) emerged in China and led to a worldwide pandemic of the disease termed Coronavirus Disease 2019 (COVID-19). The global health threat posed by this pandemic led to an extremely rapid and robust mobilization of the scientific and medical communities as evidenced by the publication of more than ten-thousand peer-reviewed articles and thousands of preprints in the first year of the pandemic alone. With the publication of the initial genome sequence of SARS-CoV-2, the proteomics community immediately joined this effort publishing, to date, more than 100 peer-reviewed proteomics studies and submitting many more preprints to preprint servers. In this review, we focus on peer-reviewed articles published on the proteome, glycoproteome, and glycome of SARS-CoV-2. At a basic level, proteomic studies provide valuable information on quantitative aspects of viral infection course; information on the identities, sites, and microheterogeneity of post-translational modifications; and, information on protein-protein interactions. At a biological systems level, these studies elucidate host cell and tissue responses, characterize antibodies and other immune system factors in infection, suggest biomarkers that may be useful for diagnosis and disease-course monitoring, and help in the development or repurposing of potential therapeutics. Here, we summarize results from selected early studies to provide a perspective on the current rapidly evolving literature.

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          Most cited references130

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          Clinical features of patients infected with 2019 novel coronavirus in Wuhan, China

          Summary Background A recent cluster of pneumonia cases in Wuhan, China, was caused by a novel betacoronavirus, the 2019 novel coronavirus (2019-nCoV). We report the epidemiological, clinical, laboratory, and radiological characteristics and treatment and clinical outcomes of these patients. Methods All patients with suspected 2019-nCoV were admitted to a designated hospital in Wuhan. We prospectively collected and analysed data on patients with laboratory-confirmed 2019-nCoV infection by real-time RT-PCR and next-generation sequencing. Data were obtained with standardised data collection forms shared by WHO and the International Severe Acute Respiratory and Emerging Infection Consortium from electronic medical records. Researchers also directly communicated with patients or their families to ascertain epidemiological and symptom data. Outcomes were also compared between patients who had been admitted to the intensive care unit (ICU) and those who had not. Findings By Jan 2, 2020, 41 admitted hospital patients had been identified as having laboratory-confirmed 2019-nCoV infection. Most of the infected patients were men (30 [73%] of 41); less than half had underlying diseases (13 [32%]), including diabetes (eight [20%]), hypertension (six [15%]), and cardiovascular disease (six [15%]). Median age was 49·0 years (IQR 41·0–58·0). 27 (66%) of 41 patients had been exposed to Huanan seafood market. One family cluster was found. Common symptoms at onset of illness were fever (40 [98%] of 41 patients), cough (31 [76%]), and myalgia or fatigue (18 [44%]); less common symptoms were sputum production (11 [28%] of 39), headache (three [8%] of 38), haemoptysis (two [5%] of 39), and diarrhoea (one [3%] of 38). Dyspnoea developed in 22 (55%) of 40 patients (median time from illness onset to dyspnoea 8·0 days [IQR 5·0–13·0]). 26 (63%) of 41 patients had lymphopenia. All 41 patients had pneumonia with abnormal findings on chest CT. Complications included acute respiratory distress syndrome (12 [29%]), RNAaemia (six [15%]), acute cardiac injury (five [12%]) and secondary infection (four [10%]). 13 (32%) patients were admitted to an ICU and six (15%) died. Compared with non-ICU patients, ICU patients had higher plasma levels of IL2, IL7, IL10, GSCF, IP10, MCP1, MIP1A, and TNFα. Interpretation The 2019-nCoV infection caused clusters of severe respiratory illness similar to severe acute respiratory syndrome coronavirus and was associated with ICU admission and high mortality. Major gaps in our knowledge of the origin, epidemiology, duration of human transmission, and clinical spectrum of disease need fulfilment by future studies. Funding Ministry of Science and Technology, Chinese Academy of Medical Sciences, National Natural Science Foundation of China, and Beijing Municipal Science and Technology Commission.
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            A Novel Coronavirus from Patients with Pneumonia in China, 2019

            Summary In December 2019, a cluster of patients with pneumonia of unknown cause was linked to a seafood wholesale market in Wuhan, China. A previously unknown betacoronavirus was discovered through the use of unbiased sequencing in samples from patients with pneumonia. Human airway epithelial cells were used to isolate a novel coronavirus, named 2019-nCoV, which formed a clade within the subgenus sarbecovirus, Orthocoronavirinae subfamily. Different from both MERS-CoV and SARS-CoV, 2019-nCoV is the seventh member of the family of coronaviruses that infect humans. Enhanced surveillance and further investigation are ongoing. (Funded by the National Key Research and Development Program of China and the National Major Project for Control and Prevention of Infectious Disease in China.)
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              Is Open Access

              A pneumonia outbreak associated with a new coronavirus of probable bat origin

              Since the outbreak of severe acute respiratory syndrome (SARS) 18 years ago, a large number of SARS-related coronaviruses (SARSr-CoVs) have been discovered in their natural reservoir host, bats 1–4 . Previous studies have shown that some bat SARSr-CoVs have the potential to infect humans 5–7 . Here we report the identification and characterization of a new coronavirus (2019-nCoV), which caused an epidemic of acute respiratory syndrome in humans in Wuhan, China. The epidemic, which started on 12 December 2019, had caused 2,794 laboratory-confirmed infections including 80 deaths by 26 January 2020. Full-length genome sequences were obtained from five patients at an early stage of the outbreak. The sequences are almost identical and share 79.6% sequence identity to SARS-CoV. Furthermore, we show that 2019-nCoV is 96% identical at the whole-genome level to a bat coronavirus. Pairwise protein sequence analysis of seven conserved non-structural proteins domains show that this virus belongs to the species of SARSr-CoV. In addition, 2019-nCoV virus isolated from the bronchoalveolar lavage fluid of a critically ill patient could be neutralized by sera from several patients. Notably, we confirmed that 2019-nCoV uses the same cell entry receptor—angiotensin converting enzyme II (ACE2)—as SARS-CoV.
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                Author and article information

                Journal
                Mol Cell Proteomics
                Mol Cell Proteomics
                Molecular & Cellular Proteomics : MCP
                THE AUTHORS. Published by Elsevier Inc on behalf of American Society for Biochemistry and Molecular Biology.
                1535-9476
                1535-9484
                4 June 2021
                4 June 2021
                : 100103
                Affiliations
                [1]Complex Carbohydrate Research Center, University of Georgia, Athens, GA, USA
                Author notes
                []Correspondence:
                Article
                S1535-9476(21)00076-1 100103
                10.1016/j.mcpro.2021.100103
                8176883
                34089862
                4630beb6-c8b3-42bc-9161-e04afd56ba9c
                © 2021 The Authors

                Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.

                History
                : 4 May 2021
                : 24 May 2021
                Categories
                Review

                Molecular biology
                3clpro, (3c-like protease),ace2, (angiotensin-converting enzyme 2),adp, (adenosine diphosphate),biogrid, (biological general repository for interaction datasets),covid-19, (coronavirus disease 2019),cp, (cytoplasm),cptac, (clinical proteomic tumor analysis consortium),dda, (data-dependent acquisition),deamid, (deamidation),dia, (data-independent acquisition),e, (envelope protein),embl-ebi, (european molecular biology laboratory,european bioinformatics institute), en,(endosome), er,(endoplasmic reticulum), ergic,(endoplasmic reticulum golgi intermediate compartment), erm,(endoplasmic reticulum membrane), esp,(especially), fe-nta,(ferric nitrilotriacetate), fp,(fusion peptide), gisaid,(global initiative on sharing avian influenza data), grna,(genomic rna), hcd,(higher-energy collisional dissociation), hr1,(heptad repeat 1), hr2,(heptad repeat 2), hs,(heparan sulfate), lc-ms,(liquid chromatography, mass spectrometry),llod, (lower limit of detection),ly, (lysosome),m, (membrane protein),mavs, (mitochondrial antiviral signaling),meprod, (multiplexed enhanced protein dynamics),moi, (multiplicity of infection),mpro, (main protease),mt, (mitochondria),n, (nucleocapsid protein),ncbi, (national center for biotechnology information),nm, (nuclear membrane),nmd, (nonsense mediated decay),no, (nucleolus),nsp, (nonstructural protein),nu, (nucleus),orf, (open reading frame),oxid, (oxidation),pbmc, (peripheral blood mononuclear cell),pcr, (polymerase chain reaction),plpro, (papain-like protease),pm, (plasma membrane),pn, (perinuclear),ppi, (protein-protein interaction),prm, (parallel reaction monitoring),ptm, (post-translational modification),qpcr, (quantitative polymerase chain reaction),rbd, (receptor binding domain),rnp, (ribonucleoprotein),rplc, (reversed phase liquid chromatography),s, (spike or surface glycoprotein),sars, (severe acute respiratory syndrome),sars-cov-1, (severe acute respiratory syndrome coronavirus 1),sars-cov-2, (severe acute respiratory syndrome coronavirus 2),sgrna, (subgenomic rna),silac, (stable isotope labeling by amino acids in cell culture),ss-rna, (single-stranded rna),tmt, (tandem mass tag)
                Molecular biology
                3clpro, (3c-like protease), ace2, (angiotensin-converting enzyme 2), adp, (adenosine diphosphate), biogrid, (biological general repository for interaction datasets), covid-19, (coronavirus disease 2019), cp, (cytoplasm), cptac, (clinical proteomic tumor analysis consortium), dda, (data-dependent acquisition), deamid, (deamidation), dia, (data-independent acquisition), e, (envelope protein), embl-ebi, (european molecular biology laboratory, european bioinformatics institute), en, (endosome), er, (endoplasmic reticulum), ergic, (endoplasmic reticulum golgi intermediate compartment), erm, (endoplasmic reticulum membrane), esp, (especially), fe-nta, (ferric nitrilotriacetate), fp, (fusion peptide), gisaid, (global initiative on sharing avian influenza data), grna, (genomic rna), hcd, (higher-energy collisional dissociation), hr1, (heptad repeat 1), hr2, (heptad repeat 2), hs, (heparan sulfate), lc-ms, (liquid chromatography, mass spectrometry), llod, (lower limit of detection), ly, (lysosome), m, (membrane protein), mavs, (mitochondrial antiviral signaling), meprod, (multiplexed enhanced protein dynamics), moi, (multiplicity of infection), mpro, (main protease), mt, (mitochondria), n, (nucleocapsid protein), ncbi, (national center for biotechnology information), nm, (nuclear membrane), nmd, (nonsense mediated decay), no, (nucleolus), nsp, (nonstructural protein), nu, (nucleus), orf, (open reading frame), oxid, (oxidation), pbmc, (peripheral blood mononuclear cell), pcr, (polymerase chain reaction), plpro, (papain-like protease), pm, (plasma membrane), pn, (perinuclear), ppi, (protein-protein interaction), prm, (parallel reaction monitoring), ptm, (post-translational modification), qpcr, (quantitative polymerase chain reaction), rbd, (receptor binding domain), rnp, (ribonucleoprotein), rplc, (reversed phase liquid chromatography), s, (spike or surface glycoprotein), sars, (severe acute respiratory syndrome), sars-cov-1, (severe acute respiratory syndrome coronavirus 1), sars-cov-2, (severe acute respiratory syndrome coronavirus 2), sgrna, (subgenomic rna), silac, (stable isotope labeling by amino acids in cell culture), ss-rna, (single-stranded rna), tmt, (tandem mass tag)

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