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Sulfated Glycans Inhibit the Interaction of MERS-CoV Receptor Binding Domain with Heparin
Jiyuan Yang1,2, Yuefan Song2, Weihua Jin3
1The Key Laboratory of Molecular Microbiology and Technology, Ministry of Education, College of Life Sciences, Nankai University, Tianjin 300071, China.
Abstract:
Middle East respiratory syndrome coronavirus (MERS-CoV) is a zoonotic virus with high contagion and mortality rates. Heparan sulfate proteoglycans (HSPGs) are ubiquitously expressed on the surface of mammalian cells. Owing to its high negatively charged property, heparan sulfate (HS) on the surface of host cells is used by many viruses as cofactor to facilitate viral attachment and initiate cellular entry. Therefore, inhibition of the interaction between viruses and HS could be a promising target to inhibit viral infection. In the current study, the interaction between the receptor-binding domain (RBD) of MERS-CoV and heparin was exploited to assess the inhibitory activity of various sulfated glycans such as glycosaminoglycans, marine-sourced glycans (sulfated fucans, fucosylated chondroitin sulfates, fucoidans, and rhamnan sulfate), pentosan polysulfate, and mucopolysaccharide using Surface Plasmon Resonance. We believe this study provides valuable insights for the development of sulfated glycan-based inhibitors as potential antiviral agents.
Insights
Researchers explored how sulfated glycans can inhibit Middle East respiratory syndrome coronavirus (MERS-CoV) by blocking its attachment to host cells. This study offers insights into developing new antiviral agents targeting MERS-CoV infection.
Area of Science:
- Virology
- Glycobiology
- Biochemistry
Background:
- Middle East respiratory syndrome coronavirus (MERS-CoV) is a highly contagious and lethal zoonotic virus.
- Heparan sulfate proteoglycans (HSPGs) on mammalian cell surfaces are crucial for viral entry.
- Inhibiting virus-HSPG interactions presents a potential antiviral strategy.
Purpose of the Study:
- To investigate the inhibitory potential of various sulfated glycans against MERS-CoV.
- To assess the interaction between the MERS-CoV receptor-binding domain (RBD) and heparin.
- To explore sulfated glycans as potential antiviral agents.
Main Methods:
- Surface Plasmon Resonance (SPR) was used to analyze interactions.
- The binding of MERS-CoV RBD to heparin was studied.
- The inhibitory effects of diverse sulfated glycans were evaluated.
Main Results:
- The study successfully exploited the MERS-CoV RBD-heparin interaction.
- Various sulfated glycans demonstrated inhibitory activity.
- Insights into the mechanism of MERS-CoV attachment were gained.
Conclusions:
- Sulfated glycans show promise as inhibitors of MERS-CoV infection.
- Targeting the virus-HS interaction is a viable antiviral approach.
- This research supports the development of novel sulfated glycan-based MERS-CoV inhibitors.
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