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Protein Posttranslational Signatures Identified in COVID-19 Patient Plasma.
Vedula, Pavan; Tang, Hsin-Yao; Speicher, David W; Kashina, Anna.
  • Vedula P; Department of Biomedical Sciences, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA, United States.
  • Tang HY; The Wistar Institute, Philadelphia, PA, United States.
  • Speicher DW; The Wistar Institute, Philadelphia, PA, United States.
  • Kashina A; Department of Biomedical Sciences, University of Pennsylvania School of Veterinary Medicine, Philadelphia, PA, United States.
Front Cell Dev Biol ; 10: 807149, 2022.
Article in English | MEDLINE | ID: covidwho-1714988
ABSTRACT
Severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) is a highly contagious virus of the coronavirus family that causes coronavirus disease-19 (COVID-19) in humans and a number of animal species. COVID-19 has rapidly propagated in the world in the past 2 years, causing a global pandemic. Here, we performed proteomic analysis of plasma samples from COVID-19 patients compared to healthy control donors in an exploratory study to gain insights into protein-level changes in the patients caused by SARS-CoV-2 infection and to identify potential proteomic and posttranslational signatures of this disease. Our results suggest a global change in protein processing and regulation that occurs in response to SARS-CoV-2, and the existence of a posttranslational COVID-19 signature that includes an elevation in threonine phosphorylation, a change in glycosylation, and a decrease in arginylation, an emerging posttranslational modification not previously implicated in infectious disease. This study provides a resource for COVID-19 researchers and, longer term, and will inform our understanding of this disease and its treatment.
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Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Front Cell Dev Biol Year: 2022 Document Type: Article Affiliation country: Fcell.2022.807149

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Full text: Available Collection: International databases Database: MEDLINE Language: English Journal: Front Cell Dev Biol Year: 2022 Document Type: Article Affiliation country: Fcell.2022.807149