Biological and molecular docking studies on coagulin-H: Human IL-2 novel natural inhibitor

Mol Immunol. 2006 Apr;43(11):1855-63. doi: 10.1016/j.molimm.2005.10.020. Epub 2006 Jan 10.

Abstract

Withanolide, coagulin-H (1), was evaluated for its effect on various cellular functions related to immune response including lymphocyte proliferation, and expression of interleukin-2 (IL-2) cytokine, and results were compared with prednisolone (2), a commonly used immune modulating drug. Coagulin-H (1) was found to have a powerful inhibitory effect on lymphocyte proliferation and Th-1 cytokine production. Inhibition of the phytohaemagglutinin (PHA)-activated T-cell proliferation by coagulin-H (1) was observed in a concentration dependent manner. A complete suppression of PHA-activated T-cell was observed at > or =2.5 microg/mL concentrations of compound (1) and this suppression activity was similar to that of prednisolone (2). Coagulin-H (1) also significantly inhibited IL-2 production by 80%. The interactions of coagulin-H (1) (a natural inhibitor) and prednisolone (2) (a drug) to IL-2 were also investigated in order to understand the differences in their effects on T-cell responses. This paper also describes the results of molecular docking study on IL-2 inhibition. Docking studies predicted that coagulin-H (1) binds to receptor binding site of IL-2 more effectively than prednisolone (2). Based on the computational and the experimental results, coagulin-H (1) was identified as a potential immunosuppressive candidate.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Binding Sites
  • Cattle
  • Cell Proliferation / drug effects
  • Cytotoxicity, Immunologic
  • DNA / biosynthesis
  • Humans
  • Interleukin-2 / antagonists & inhibitors
  • Interleukin-2 / chemistry*
  • Interleukin-2 / metabolism*
  • Lymphokines / chemistry
  • Lymphokines / metabolism*
  • Lymphokines / pharmacology*
  • Models, Molecular
  • Monocytes / drug effects
  • Monocytes / metabolism
  • Phytohemagglutinins / immunology
  • Prednisolone / chemistry
  • Prednisolone / pharmacology
  • Protein Binding
  • Protein Conformation
  • T-Lymphocytes / cytology
  • T-Lymphocytes / drug effects*
  • T-Lymphocytes / immunology
  • Thromboplastin / chemistry*
  • Thromboplastin / metabolism
  • Thromboplastin / pharmacology*

Substances

  • Interleukin-2
  • Lymphokines
  • Phytohemagglutinins
  • interleukin 2 inhibitor
  • DNA
  • Thromboplastin
  • Prednisolone