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

被引:21
|
作者
Suntravat, Montamas [1 ]
Cromer, Walter E. [2 ]
Marquez, Jessenia [1 ]
Galan, Jacob A. [1 ]
Zawieja, David C. [2 ]
Davies, Peter [3 ]
Salazar, Emelyn [1 ]
Sanchez, Elda E. [1 ,4 ]
机构
[1] Texas A&M Univ, Natl Nat Toxins Res Ctr, 975 W Ave B, Kingsville, TX 78363 USA
[2] Texas A&M Hlth Sci Ctr, Dept Med Physiol, Temple, TX USA
[3] Texas A&M Univ, Inst Biosci & Technol, Houston, TX USA
[4] Texas A&M Univ, Dept Chem, Kingsville, TX USA
基金
美国国家卫生研究院;
关键词
Snake venom; Southern pacific rattlesnake; Snake venom cysteine-rich secretory protein (svCRiSP); Vascular permeability; Vasculature; Lymphatic cells; ANTI-ANGIOGENIC ACTIVITIES; CYTOSKELETON; NEUTROPHILS; HISTAMINE; TARGETS; CLONING; NATRIN; CANCER;
D O I
10.1016/j.toxicon.2019.04.006
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
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.
引用
收藏
页码:22 / 30
页数:9
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