Results 31 to 40 of about 90,748 (118)

Prion-like Domains in Spike Protein of SARS-CoV-2 Differ across Its Variants and Enable Changes in Affinity to ACE2

open access: yesMicroorganisms, 2022
Currently, the world is struggling with the coronavirus disease 2019 (COVID-19) pandemic, caused by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2).
George Tetz, Victor Tetz
doaj   +1 more source

SARS-CoV-2 spike protein displays sequence similarities with paramyxovirus surface proteins; a bioinformatics study.

open access: yesPLoS ONE, 2021
Recent emergence of SARS-CoV-2 and associated COVID-19 pandemic have posed a great challenge for the scientific community. In this study, we performed bioinformatic analyses on SARS-CoV-2 protein sequences, trying to unravel potential molecular ...
Ehsan Ahmadi   +4 more
doaj   +1 more source

FASN inhibitor TVB-3166 prevents S-acylation of the spike protein of human coronaviruses

open access: yesJournal of Lipid Research, 2022
The spike protein of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) and other coronaviruses mediates host cell entry and is S-acylated on multiple phylogenetically conserved cysteine residues.
Katrina Mekhail   +13 more
doaj   +1 more source

Emergence of SARS‐CoV‐2 spike protein at the vaccination site

open access: yesImmunity, Inflammation and Disease, 2023
Background The anti‐coronavirus disease 2019 (COVID‐19) vaccines are of paramount importance in the fight against the COVID‐19 pandemic. Both viral vector‐ and nucleic acid‐based vaccines are known to effectively induce protection against the severe ...
Annika Beck   +4 more
doaj   +1 more source

SARS‐CoV‐2 spike protein harnesses SNX27‐mediated endocytic recycling pathway

open access: yesMedComm, 2021
SARS‐CoV‐2 is an enveloped positive‐sense RNA virus that depends on host factors for all stages of its life. Membrane receptor ACE2 is a well‐established factor for SARS‐CoV‐2 docking.
Lin Zhao   +5 more
doaj   +1 more source

Site Density Functional Theory and Structural Bioinformatics Analysis of the SARS-CoV Spike Protein and hACE2 Complex

open access: yesMolecules, 2022
The entry of the SARS-CoV-2, a causative agent of COVID-19, into human host cells is mediated by the SARS-CoV-2 spike (S) glycoprotein, which critically depends on the formation of complexes involving the spike protein receptor-binding domain (RBD) and ...
Nitesh Kumawat   +9 more
doaj   +1 more source

Design, Construction and Expression of Spike Highly Conserved Region (HCR) SARS-CoV-2 and Cholera Toxin Subunit B Fusion Protein in Lactococcus lactis NZ3900

open access: yesJournal of Tropical Life Science
Prevention of SARS-CoV-2 transmission has primarily been achieved through vaccination, which is generally administered via injection and may cause discomfort.
Suryanata Kesuma   +4 more
doaj   +1 more source

SARS-CoV-2 spike fusion peptide trans interaction with phosphatidylserine lipid triggers membrane fusion for viral entry

open access: yesmBio
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) spike is the fusion machine for host cell entry. Still, the mechanism by which spike protein interacts with the target lipid membrane to facilitate membrane fusion during entry is not fully ...
Puspangana Singh   +6 more
doaj   +1 more source

A new DNA aptamer which binds to SARS-CoV-2 spike protein and reduces pro-inflammatory response

open access: yesScientific Reports
COVID-19 caused by SARS-CoV-2 spread rapidly around the world, endangering the health of people globally. The SARS-CoV-2 spike protein initiates entry into target cells by binding to human angiotensin-converting enzyme 2 (ACE2).
Woong Kim   +5 more
doaj   +1 more source

Determinants of susceptibility to SARS-CoV-2 infection in murine ACE2

open access: yesJournal of Virology
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) utilizes angiotensin-converting enzyme 2 (ACE2) as a receptor to enter host cells, and primary receptor recognition of the spike protein is a major determinant of the host range of SARS-CoV-2 ...
Takashi Kondo   +10 more
doaj   +1 more source

Home - About - Disclaimer - Privacy