Intrinsic factors behind long COVID: IV. Hypothetical roles of the SARS-CoV-2 nucleocapsid protein and its liquid-liquid phase separation.
Ahmed EltayebFaisal Al-SarrajMona AlharbiRaed S AlbiheyriEhab H MattarIsam M Abu ZeidThamer A BoubackAtif BamagoosVladimir N UverskyAlberto Rubio-CasillasElrashdy Mustafa RedwanPublished in: Journal of cellular biochemistry (2024)
When the SARS-CoV-2 virus infects humans, it leads to a condition called COVID-19 that has a wide spectrum of clinical manifestations, from no symptoms to acute respiratory distress syndrome. The virus initiates damage by attaching to the ACE-2 protein on the surface of endothelial cells that line the blood vessels and using these cells as hosts for replication. Reactive oxygen species levels are increased during viral replication, which leads to oxidative stress. About three-fifths (~60%) of the people who get infected with the virus eradicate it from their body after 28 days and recover their normal activity. However, a large fraction (~40%) of the people who are infected with the virus suffer from various symptoms (anosmia and/or ageusia, fatigue, cough, myalgia, cognitive impairment, insomnia, dyspnea, and tachycardia) beyond 12 weeks and are diagnosed with a syndrome called long COVID. Long-term clinical studies in a group of people who contracted SARS-CoV-2 have been contrasted with a noninfected matched group of people. A subset of infected people can be distinguished by a set of cytokine markers to have persistent, low-grade inflammation and often self-report two or more bothersome symptoms. No medication can alleviate their symptoms efficiently. Coronavirus nucleocapsid proteins have been investigated extensively as potential drug targets due to their key roles in virus replication, among which is their ability to bind their respective genomic RNAs for incorporation into emerging virions. This review highlights basic studies of the nucleocapsid protein and its ability to undergo liquid-liquid phase separation. We hypothesize that this ability of the nucleocapsid protein for phase separation may contribute to long COVID. This hypothesis unlocks new investigation angles and could potentially open novel avenues for a better understanding of long COVID and treating this condition.
Keyphrases
- sars cov
- respiratory syndrome coronavirus
- oxidative stress
- coronavirus disease
- acute respiratory distress syndrome
- low grade
- sleep quality
- endothelial cells
- protein protein
- cognitive impairment
- induced apoptosis
- binding protein
- amino acid
- reactive oxygen species
- extracorporeal membrane oxygenation
- cell proliferation
- intensive care unit
- mechanical ventilation
- multidrug resistant
- dna methylation
- minimally invasive
- signaling pathway
- cell death
- mass spectrometry
- cell cycle arrest
- single molecule
- small molecule
- atrial fibrillation
- angiotensin ii
- climate change
- depressive symptoms
- atomic force microscopy
- gestational age