Skip to content
Research Article Open access CC BY 4.0

Analyses of the Spike Proteins of Severe Acute Respiratory Syndrome-Related Coronaviruses

Peramachi Palanivelu

Microbiology Research Journal International · pp. 32–50 · Published 24 Sep 2020

10.9734/mrji/2020/v30i830249

Abstract

Aim: To analyze spike proteins of Severe Acute Respiratory Syndrome (SARS)-related coronaviruses (CoVs) for their conserved motifs, Receptor-Binding  Domain (RBD), Receptor Binding Motif (RBM) of SARS-CoV (CoV-1), SARS-CoV-2, Middle East Respiratory Syndrome (MERS)-CoV and their relationship to the bat, pangolin and palm civet-CoVs as possible intermediate hosts. Study Design: Multiple sequence analysis (MSA) of spike proteins of different SARS-CoVs were studied using Clustal Omega and ExPASy tools. Methodology: Bioinformatics, SDM and X-ray crystallographic data of the spike proteins from different CoVs including the current epidemic causing SARS-CoV-2 were analyzed. The advanced version of Clustal Omega was used for protein sequence analysis of different spike proteins from various CoVs and ExPASy tool was used for pI analysis. Results: Spike proteins in coronaviruses play important roles in mediating receptor binding, membrane fusion, and viral entry into human cells. Furthermore, nowadays all the vaccine development programmes are mainly focused on the SARS-CoV-2 spike protein only, as it plays the crucial, first step in the infection process. Therefore, the spike proteins of the SARS-related coronaviruses, the main determinant of coronavirus host specificity, are analyzed for their conserved motifs, RBD, RBM, etc. The recent epidemic causing strain, SARS-CoV-2, showed 2 dipeptide deletions and 4 peptide insertions ranging from tetra- to hepta-peptides in its spike protein as compared to its predecessor CoV-1. Most of the insertions are also found in the bat and pangolin CoVs except one unique tetrapeptide. The RBM region shows that the bats, pangolins and CoV-2 exhibit very similar to identical sequences. The overall analyses show that the latest SARS-CoV-2 is related to bats and more to pangolin-CoVs suggesting that the pangolins could be possibly the intermediate host. On the other hand, it is found that palm civet RBM sequences are highly related to CoV-1 and not CoV-2. Possibly the novel CoV-2 would have taken three insertions from bats and/or pangolins and the fourth insertion –PRRA- which is unique to SARS-CoV-2 is critically placed just in the S1/S2 cleavage region. The recently discovered G614 mutation (D614→G) in CoV-2, the most prevalent form in the global pandemic now, is found near the RBD towards the C-terminal. Placement of the unique tetrapeptide in the S1/S2 loop region and replacement with more positive charges on the spike protein which resulted in marked increase in the basicity of the SARS-CoV-2 spike protein may, possibly result in significant effects on the structure and function of the protein, possibly leading to rapid transmission. Conclusions: RBD and RBM regions of the spike proteins of SARS-CoV-1 and palm civet show very close identity to each other whereas the SARS-CoV-2, pangolin- and bat-CoVs exhibit very close identities in their RBD and RBM regions. The two crucial modifications in the spike protein of SARS-CoV-2, viz. a marked increase in the basicity of the protein and the insertion of a dibasic tetrapeptide (–PRRA-) at the critical S1/S2 cleavage point possibly make it to bind to the ACE2 receptor with higher affinity and get it cleaved by the host proteases more efficiently with subsequent effective internalization of the viral genome.

Coronaviruses Severe Acute Respiratory Syndrome SARS-CoV-1 MERS-CoV SARS-CoV-2 Bat-CoV Pangolin-CoVs Palm civet-CoVs.

References (24)

  1. 1 A new coronavirus associated with human respiratory disease in China [DOI]
  2. 2 Structure of the SARS-CoV-2 spike receptor-binding domain bound to the ACE2 receptor [DOI]
  3. 3 Angiotensin-converting enzyme 2 is a functional receptor for the SARS coronavirus [DOI]
  4. 4 Clinical and immunological features of severe and moderate coronavirus disease 2019 [DOI]
  5. 5 Coronaviruses: An Overview of Their Replication and Pathogenesis [DOI]
  6. 6 Dipeptidyl peptidase 4 is a functional receptor for the emerging human coronavirus-EMC [DOI]
  7. 7 Identifying SARS-CoV-2-related coronaviruses in Malayan pangolins [DOI]
  8. 8 A Multibasic Cleavage Site in the Spike Protein of SARS-CoV-2 Is Essential for Infection of Human Lung Cells [DOI]
  9. 9 Site-specific glycan analysis of the SARS-CoV-2 spike [DOI]
  10. 10 Hydrolysis of Biological Peptides by Human Angiotensin-converting Enzyme-related Carboxypeptidase [DOI]
  11. 11 Human aminopeptidase N is a receptor for human coronavirus 229E [DOI]
  12. 12 Human coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry [DOI]
  13. 13 TMPRSS2 and furin are both essential for proteolytic activation of SARS-CoV-2 in human airway cells [DOI]
  14. 14 Influenza virus hemagglutinin with multibasic cleavage site is activated by furin, a subtilisin‐like endoprotease. [DOI]
  15. 15 History and Recent Advances in Coronavirus Discovery [DOI]
  16. 16 Are pangolins the intermediate host of the 2019 novel coronavirus (SARS-CoV-2)? [DOI]
  17. 17 Gene Flow of a Forest-Dependent Bird across a Fragmented Landscape [DOI]
  18. 18 Sars‐CoV‐2 Envelope and Membrane Proteins: Structural Differences Linked to Virus Characteristics? [DOI]
  19. 19 Coronaviruses, a New Group of Animal RNA Viruses [DOI]
  20. 20 Receptor-binding domain as a target for developing SARS vaccines. [DOI]
  21. 21 RNA Recombination of Coronavirus [DOI]
  22. 22 RNA recombination in a coronavirus: recombination between viral genomic RNA and transfected RNA fragments [DOI]
  23. 23 History and Recent Advances in Coronavirus Discovery [DOI]
  24. 24 Analyses of Homing Endonucleases and Mechanism of Action of CRISPR-Cas9 HNH Endonucleases [DOI]

Cited by 6

An Overview of the Proofreading Functions in Bacteria and in Severe Acute Respiratory Syndrome-Coronaviruses

Peramachi Palanivelu · International Journal of Biochemistry Research & Review · 2021

Showing 4 of 6 known citations — external sources report more than can currently be individually listed.

Article metrics

Real usage data collected on this platform.

48

Page views

0

PDF downloads

5

Outbound clicks

6

Citations

Views over time

Views by country

Approximate, from request IP at view time — not citizenship or institution. Countries with fewer than 5 views are grouped as "Other".

Traffic sources

Referring site, by host.

Views and downloads exclude known bots/crawlers. Citations combines this platform's own DOI-resolved index with each external source's own reported total — see Cited by above for individually listed citing works. Last refreshed 0 seconds ago.