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Role of Electrostatic Hotspots in the Selectivity of Complement Control Proteins Toward Human and Bovine Complement
Yogesh B Narkhede1, Avneesh K Gautam2, Rohaine V Hsu1
1Department of Bioengineering, University of California, Riverside, CA.
Abstract:
Poxviruses are dangerous pathogens, which can cause fatal infection in unvaccinated individuals. The causative agent of smallpox in humans, variola virus, is closely related to the bovine vaccinia virus, yet the molecular basis of their selectivity is currently incompletely understood. Here, we examine the role of the electrostatics in the selectivity of the smallpox protein SPICE and vaccinia protein VCP toward the human and bovine complement protein C3b, a key component of the complement immune response. Electrostatic calculations, in-silico alanine-scan and electrostatic hotspot analysis, as introduced by Kieslich and Morikis (PLoS Comput. Biol. 2012), are used to assess the electrostatic complementarity and to identify sites resistant to local perturbation where the electrostatic potential is likely to be evolutionary conserved. The calculations suggest that the bovine C3b is electrostatically prone to selectively bind its VCP ligand. On the other hand, the human isoform of C3b exhibits a lower electrostatic complementarity toward its SPICE ligand. Yet, the human C3b displays a highly preserved electrostatic core, which suggests that this isoform could be less selective in binding different ligands like SPICE and the human Factor H. This is supported by experimental cofactor activity assays revealing that the human C3b is prone to bind both SPICE and Factor H, which exhibit diverse electrostatic properties. Additional investigations considering mutants of SPICE and VCP that revert their selectivity reveal an "electrostatic switch" into the central modules of the ligands, supporting the critical role of the electrostatics in the selectivity. Taken together, these evidences provide insights into the selectivity mechanism of the complement regulator proteins encoded by the variola and vaccinia viruses to circumvent the complement immunity and exert their pathogenic action. These fundamental aspects are valuable for the development of novel vaccines and therapeutic strategies.
Insights
Poxvirus proteins SPICE and VCP show selective binding to complement protein C3b. Electrostatic interactions explain how these viruses evade the immune system, aiding vaccine development.
Area of Science:
- Virology and Immunology
- Computational Biology
- Structural Biology
Background:
- Poxviruses, including variola virus (smallpox) and vaccinia virus, are significant pathogens.
- Understanding their molecular mechanisms for evading host immunity is crucial for developing countermeasures.
- The complement system, particularly complement protein C3b, is a key target for viral immune evasion.
Purpose of the Study:
- To investigate the role of electrostatics in the selective binding of viral proteins (SPICE, VCP) to human and bovine complement protein C3b.
- To identify conserved electrostatic features that may influence ligand selectivity and viral immune evasion strategies.
Main Methods:
- In-silico electrostatic calculations, including alanine-scan and electrostatic hotspot analysis.
- Computational assessment of electrostatic complementarity between viral proteins and C3b isoforms.
- Experimental cofactor activity assays to validate computational findings.
Main Results:
- Bovine C3b exhibits stronger electrostatic complementarity to VCP (vaccinia virus) than human C3b does to SPICE (variola virus).
- Human C3b shows less selective binding due to a conserved electrostatic core, interacting with both SPICE and Factor H.
- Mutational analysis revealed an "electrostatic switch" mechanism critical for ligand selectivity.
Conclusions:
- Electrostatic interactions are fundamental to the selective binding of poxviral complement regulators (SPICE, VCP) to C3b.
- These findings elucidate viral strategies for circumventing complement immunity.
- The insights gained are valuable for designing novel vaccines and therapeutics against poxviruses.
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