The isolation and characterization of a new snake venom cysteine-rich secretory protein (svCRiSP) from the venom of the Southern Pacific rattlesnake and its effect on vascular permeability

Toxicon. 2019 Jul:165:22-30. doi: 10.1016/j.toxicon.2019.04.006. Epub 2019 Apr 20.

Abstract

A novel snake venom cysteine-rich secretory protein (svCRiSP), Hellerin, was purified from C. o. helleri venom using sequential reverse phase and cation-exchange chromatography. Gel electrophoresis, N-terminal sequencing, and LC-MS/MS sequencing identified a single protein with a molecular mass of approximately 24.8 kDa and confirmed its identity as a svCRiSP. Hellerin had cytotoxic effects on human umbilical vein endothelial cells (HUVECs) in a dose-dependent manner but not in human dermal lymphatic endothelial cells (HDLECs) and human dermal blood endothelial cells (HDBECs). Hellerin produced a dramatic increase in both blood vascular permeability in vivo, and in the trans-epithelial permeability of cultured HDLEC and HDBEC cells. This is the first study that describes the effect of a svCRiSP on vascular, blood and lymphatic permeability.

Keywords: Lymphatic cells; Snake venom; Snake venom cysteine-rich secretory protein (svCRiSP); Southern pacific rattlesnake; Vascular permeability; Vasculature.

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Capillary Permeability / drug effects*
  • Cell Line
  • Chromatography, Liquid
  • Crotalid Venoms / chemistry*
  • Crotalid Venoms / isolation & purification
  • Crotalus
  • Cysteine
  • Human Umbilical Vein Endothelial Cells
  • Humans
  • Reptilian Proteins / chemistry
  • Reptilian Proteins / isolation & purification
  • Reptilian Proteins / pharmacology*
  • Sequence Alignment
  • Tandem Mass Spectrometry

Substances

  • Crotalid Venoms
  • Reptilian Proteins
  • Cysteine