Virtual Probing on the Influence of Ca 2+ and Zn 2+ Bound S100A8 and S100A9 Proteins Towards their Interaction Against Pattern Recognition Receptors Aggravating Rheumatoid Arthritis.

Autor: Paramasivam S; Department of Pharmaceutical Technology, University College of Engineering, Bharathidasan Institute of Technology campus, Anna University, Tiruchirappalli, 620 024, Tamil Nadu, India., Murugesan J; Medical Genomics lab, Department of Bioinformatics, Bharathiar University, Coimbatore, 641 046, India., Vedagiri H; Medical Genomics lab, Department of Bioinformatics, Bharathiar University, Coimbatore, 641 046, India., Perumal SS; Department of Pharmaceutical Technology, University College of Engineering, Bharathidasan Institute of Technology campus, Anna University, Tiruchirappalli, 620 024, Tamil Nadu, India., Ekambaram SP; Department of Pharmaceutical Technology, University College of Engineering, Bharathidasan Institute of Technology campus, Anna University, Tiruchirappalli, 620 024, Tamil Nadu, India. sanmugapriya77@aubit.edu.in.
Jazyk: angličtina
Zdroj: Cell biochemistry and biophysics [Cell Biochem Biophys] 2024 Nov 22. Date of Electronic Publication: 2024 Nov 22.
DOI: 10.1007/s12013-024-01600-6
Abstrakt: Danger-associated molecular patterns (DAMPs) are released on the onset of tissue injury or death, which tend to trigger innate immunity and regulate various immune pathways. Among the various DAMP molecules, S100A8 and S100A9 belonging to Ca 2+ binding proteins with EF-hands and Zn 2+ ion binding sites have been implicated in aggravating the pathogenesis of rheumatoid arthritis (RA), upon interaction with pattern recognition receptors (PRR) such as TLR4, RAGE and CD36 receptors. Thus, the present study aims to assess the effect of Ca 2+ or Zn 2+ ions on the interaction of S100A8 and S100A9 proteins towards the PRRs. Protein-protein interaction analysis showed that the TLR4-S100A8Ca 2+ Zn 2+ , TLR4-S100A8 Zn 2+ , RAGE-S100A8/A8Zn 2+ , RAGE-S100A8/A8Ca 2+ , CD36-S100A8Ca 2+ , and CD36-S100A9/A9Ca 2+ showed higher affinity against each other. The 100 ns molecular dynamics simulation showed that the TLR4-S100A8Ca 2+ , RAGE-S100A8/A8Ca 2+ and CD36-S100A8Ca 2+ complexes showed minimal fluctuations in their trajectory indicating that Ca 2+ bound complexes were more stable than the other complexes. Furthermore, SPR analysis showed that S100A9 exhibited higher binding affinity towards PRRs in the presence of Ca 2+ and Zn 2+ ions. Considering the fact that physiological levels of both Ca 2+ and Zn 2+ ions play a critical role in the binding of S100A8 and S100A9 proteins against the PRRs, it can be emphasized that the S100A9 and RAGE receptors could be the critical players in the RA pathogenesis due to its impeccable binding towards the PRRs in the presence of both Ca 2+ and Zn 2+ ions. Nonetheless, further in vivo, and in vitro studies are imperative to validate these findings and identify potential targets for RA treatment.
Competing Interests: Compliance with ethical standards. Conflict of interest: The authors declare no competing interests.
(© 2024. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.)
Databáze: MEDLINE
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