Article: Binding affinity between coronavirus spike protein and human ACE2 receptor.
Computational and structural biotechnology journal
2024 Volume 23, Page(s) 759–770
Abstract: Coronaviruses (CoVs) pose a major risk to global public health due to their ability to infect diverse animal species and potential for emergence in humans. The CoV spike protein mediates viral entry into the cell and plays a crucial role in determining ... ...
Abstract | Coronaviruses (CoVs) pose a major risk to global public health due to their ability to infect diverse animal species and potential for emergence in humans. The CoV spike protein mediates viral entry into the cell and plays a crucial role in determining the binding affinity to host cell receptors. With particular emphasis on α- and β-coronaviruses that infect humans and domestic animals, current research on CoV receptor use suggests that the exploitation of the angiotensin-converting enzyme 2 (ACE2) receptor poses a significant threat for viral emergence with pandemic potential. This review summarizes the approaches used to study binding interactions between CoV spike proteins and the human ACE2 (hACE2) receptor. Solid-phase enzyme immunoassays and cell binding assays allow qualitative assessment of binding but lack quantitative evaluation of affinity. Surface plasmon resonance, Bio-layer interferometry, and Microscale Thermophoresis on the other hand, provide accurate affinity measurement through equilibrium dissociation constants (K |
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Language | English |
Publishing date | 2024-01-17 |
Publishing country | Netherlands |
Document type | Journal Article ; Review |
ZDB-ID | 2694435-2 |
ISSN | 2001-0370 |
ISSN | 2001-0370 |
DOI | 10.1016/j.csbj.2024.01.009 |
Database | MEDical Literature Analysis and Retrieval System OnLINE |
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