4.5 Article

Venom Gland Mass Spectrometry Imaging of Saw-Scaled Viper, Echis carinatus sochureki, at High Lateral Resolution

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AMER CHEMICAL SOC
DOI: 10.1021/jasms.1c00042

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资金

  1. Deutsche Forschungsgemeinschaft (DFG) [INST 162/500-1 FUGG]
  2. State of Hesse through LOEWE Center DRUID (Novel Drug Targets against Poverty-Related and Neglected Tropical Infectious Diseases)
  3. National Institute for Medical Research Development (NIMAD) of Iran [942485]
  4. Promotionskolleg Bioressourcen and Biotechnologie of the Technische Hochschule Mittelhessen
  5. Justus Liebig University Giessen

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The snake venom gland is the site for synthesis, storage, and secretion of venom. While its morphology has been studied, the cellular secretory and functional processes are still not fully understood. Using advanced mass spectrometry imaging techniques, lipids and peptides were identified in the venom gland, providing insights into its composition and potential functions.
The snake venom gland is the place for the synthesis, storage, and secretion of a complex mixture of proteins and peptides, i.e., the venom. The morphology of the gland has been revealed by classical histology and microscopic studies. However, knowledge about the gland's cellular secretory and functional processes is still incomplete and has so far been neglected by the omics disciplines. We used autofocusing atmospheric-pressure matrix-assisted laser desorption/ionization (AP-SMALDI) mass spectrometry imaging (MSI) to investigate endogenous biomolecular distributions in the venom glands of the saw-scaled viper, Echis carinatus sochureki, employing different sample preparation methods. Fresh-freezing and formalin-fixation were tested for the gland to obtain intact tissue sections. Subsequently, MSI was conducted with 12 mu m pixel resolution for both types of preparations, and the lateral distributions of the metabolites were identified. Experiments revealed that lipids belonging to the classes of PC, SM, PE, PS, PA, and TG are present in the venom gland. PC (32:0) and SM (36:1) were found to be specifically located in the areas where cells are present. The snake venom metalloprotease inhibitor pEKW (m/z 444.2233) was identified in the venom by top-down LC-MS/MS and localized by MALDI-MSI in the gland across secretory epithelial cells. The peptide can inhibit the venom's enzymatic activity during long-term storage within the venom gland. With a high degree of spectral similarities, we concluded that formalin-fixed tissue, in addition to its high ability to preserve tissue morphology, can be considered as an alternative method to fresh-frozen tissue in the case of lipid and peptide MS imaging in venom gland tissues.

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