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Localization of SARS-CoV-2 Capping Enzymes Revealed by an Antibody against the nsp10 Subunit
V. Horova, B. Landova, J. Hodek, K. Chalupsky, P. Krafcikova, D. Chalupska, V. Duchoslav, J. Weber, E. Boura, M. Klima
Language English Country Switzerland
Document type Journal Article, Research Support, Non-U.S. Gov't
Grant support
21-25280S
Grantová Agentura České Republiky
NLK
Directory of Open Access Journals
from 2009
Free Medical Journals
from 2009
PubMed Central
from 2009
Europe PubMed Central
from 2009
ProQuest Central
from 2009-01-01
Open Access Digital Library
from 2009-01-01
Open Access Digital Library
from 2009-01-01
Health & Medicine (ProQuest)
from 2009-01-01
ROAD: Directory of Open Access Scholarly Resources
from 2009
PubMed
34452352
DOI
10.3390/v13081487
Knihovny.cz E-resources
- MeSH
- COVID-19 virology MeSH
- Humans MeSH
- Methyltransferases analysis genetics metabolism MeSH
- Antibodies, Monoclonal analysis MeSH
- RNA Caps genetics metabolism MeSH
- RNA, Viral genetics metabolism MeSH
- SARS-CoV-2 chemistry enzymology genetics MeSH
- Protein Transport MeSH
- Viral Nonstructural Proteins analysis genetics metabolism MeSH
- Viral Regulatory and Accessory Proteins analysis genetics metabolism MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causative agent of the coronavirus disease-19 pandemic. One of the key components of the coronavirus replication complex are the RNA methyltransferases (MTases), RNA-modifying enzymes crucial for RNA cap formation. Recently, the structure of the 2'-O MTase has become available; however, its biological characterization within the infected cells remains largely elusive. Here, we report a novel monoclonal antibody directed against the SARS-CoV-2 non-structural protein nsp10, a subunit of both the 2'-O RNA and N7 MTase protein complexes. Using this antibody, we investigated the subcellular localization of the SARS-CoV-2 MTases in cells infected with the SARS-CoV-2.
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