Proteomic Approaches to Study SARS-CoV-2 Biology and COVID-19 Pathology.
Paige HaasMonita MuralidharanNevan J KroganRobyn M KaakeRuth HüttenhainPublished in: Journal of proteome research (2021)
The novel severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), the causative agent of coronavirus disease 2019 (COVID-19), was declared a pandemic infection in March 2020. As of December 2020, two COVID-19 vaccines have been authorized for emergency use by the U.S. Food and Drug Administration, but there are no effective drugs to treat COVID-19, and pandemic mitigation efforts like physical distancing have had acute social and economic consequences. In this perspective, we discuss how the proteomic research community can leverage technologies and expertise to address the pandemic by investigating four key areas of study in SARS-CoV-2 biology. Specifically, we discuss how (1) mass spectrometry-based structural techniques can overcome limitations and complement traditional structural approaches to inform the dynamic structure of SARS-CoV-2 proteins, complexes, and virions; (2) virus-host protein-protein interaction mapping can identify the cellular machinery required for SARS-CoV-2 replication; (3) global protein abundance and post-translational modification profiling can characterize signaling pathways that are rewired during infection; and (4) proteomic technologies can aid in biomarker identification, diagnostics, and drug development in order to monitor COVID-19 pathology and investigate treatment strategies. Systems-level high-throughput capabilities of proteomic technologies can yield important insights into SARS-CoV-2 biology that are urgently needed during the pandemic, and more broadly, can inform coronavirus virology and host biology.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- coronavirus disease
- protein protein
- mass spectrometry
- healthcare
- high throughput
- mental health
- signaling pathway
- small molecule
- emergency department
- high resolution
- label free
- physical activity
- intensive care unit
- epithelial mesenchymal transition
- cell proliferation
- climate change
- drug administration
- liver failure
- respiratory failure
- high performance liquid chromatography
- single cell
- induced apoptosis
- hepatitis b virus
- amino acid
- acute respiratory distress syndrome