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Protein Posttranslational Signatures Identified in COVID-19 Patient Plasma

  • The UPenn COVID Processing Unit

Research output: Contribution to journalArticlepeer-review

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.

Original languageEnglish (US)
Article number807149
JournalFrontiers in Cell and Developmental Biology
Volume10
DOIs
StatePublished - Feb 11 2022
Externally publishedYes

Keywords

  • COVID-19
  • arginylation
  • peptidomics
  • posttranslational modifications
  • proteomics

ASJC Scopus subject areas

  • Developmental Biology
  • Cell Biology

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