A multifaceted analysis of viperid snake venoms by two-dimensional gel electrophoresis: An approach to understanding venom proteomics

• Published in: Proteomics (Weinheim) 2005-02, Vol.5 (2), p.501-510
• Main Authors: Serrano, Solange M. T., Shannon, John D., Wang, Deyu, Camargo, Antonio C. M., Fox, Jay W.
• Format: Article
• Language: English
• Subjects: Analytical, structural and metabolic biochemistry; Animals; Biological and medical sciences; Blotting, Western; Bothrops; Bothrops - genetics; Bothrops jararaca; Chromatography, Liquid; Crotalid Venoms - analysis; Crotalid Venoms - enzymology; Crotalid Venoms - genetics; Crotalus atrox; Electrophoresis, Gel, Two-Dimensional; Electrophoresis, Polyacrylamide Gel; Fundamental and applied biological sciences. Psychology; Genetic Variation; Image Processing, Computer-Assisted; Mass Spectrometry; Metalloendopeptidases - analysis; Metalloendopeptidases - genetics; Metalloendopeptidases - metabolism; Miscellaneous; Phospholipases A - analysis; Phospholipases A - genetics; Phospholipases A - metabolism; Proteins; Proteome - analysis; Proteome - genetics; Proteomics; Serine Endopeptidases - analysis; Serine Endopeptidases - genetics; Serine Endopeptidases - metabolism; Snake venom; Trypsin - metabolism; Two-dimensional gel electrophoresis; Western blot; Zymography
• ISSN: 1615-9853; 1615-9861
• DOI: 10.1002/pmic.200400931

The complexity of Viperid venoms has long been appreciated by investigators in the fields of toxinology and medicine. However, it is only recently that the depth of that complexity has become somewhat quantitatively and qualitatively appreciated. With the resurgence of two‐dimensional gel electrophoresis (2‐DE) and the advances in mass spectrometry virtually all venom components can be visualized and identified given sufficient effort and resources. Here we present the use of 2‐DE for examining venom complexity as well as demonstrating interesting approaches to selectively delineate subpopulations of venom proteins based on particular characteristics of the proteins such as antibody cross‐reactivity or enzymatic activities. 2‐DE comparisons between venoms from different species of the same genus (Bothrops) of snake clearly demonstrated both the similarity as well as the apparent diversity among these venoms. Using liquid chromatography/tandem mass spectrometry we were able to identify regions of the two‐dimensional gels from each venom in which certain classes of proteins were found. 2‐DE was also used to compare venoms from Crotalus atrox and Bothrops jararaca. For these venoms a variety of staining/detection protocols was utilized to compare and contrast the venoms. Specifically, we used various stains to visualize subpopulations of the venom proteomes of these snakes, including Coomassie, Silver, Sypro Ruby and Pro‐Q‐Emerald. Using specific antibodies in Western blot analyses of 2‐DE of the venoms we have examined subpopulations of proteins in these venoms including the serine proteinase proteome, the metalloproteinase proteome, and the phospholipases A2 proteome. A functional assessment of the gelatinolytic activity of these venoms was also performed by zymography. These approaches have given rise to a more thorough understanding of venom complexity and the toxins comprising these venoms and provide insights to investigators who wish to focus on these venom subpopulations of proteins in future studies.