Laboratory of Biochemistry and Biophysics, Instituto Butantan, São Paulo SP 05503-900, Brazil.
Laboratory of Applied Toxinology, CeTICS, Instituto Butantan, São Paulo SP 05503-900, Brazil.
Toxins (Basel). 2019 Jul 29;11(8):448. doi: 10.3390/toxins11080448.
Ant species have specialized venom systems developed to sting and inoculate a biological cocktail of organic compounds, including peptide and polypeptide toxins, for the purpose of predation and defense. The genus comprises predatory giant ants that inoculate venom capable of causing long-lasting local pain, involuntary shaking, lymphadenopathy, and cardiac arrhythmias, among other symptoms. To deepen our knowledge about venom composition with regard to protein toxins and their roles in the chemical-ecological relationship and human health, we performed a bottom-up proteomics analysis of the crude venom of the giant ant , popularly known as the "false" tocandiras. For this purpose, we used two different analytical approaches: (i) gel-based proteomics approach, wherein the crude venom was resolved by denaturing sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) and all protein bands were excised for analysis; (ii) solution-based proteomics approach, wherein the crude venom protein components were directly fragmented into tryptic peptides in solution for analysis. The proteomic data that resulted from these two methodologies were compared against a previously annotated transcriptomic database of , and subsequently, a homology search was performed for all identified transcript products. The gel-based proteomics approach unequivocally identified nine toxins of high molecular mass in the venom, as for example, enzymes [hyaluronidase, phospholipase A1, dipeptidyl peptidase and glucose dehydrogenase/flavin adenine dinucleotide (FAD) quinone] and diverse venom allergens (homologous of the red fire ant ) and venom-related proteins (major royal jelly-like). Moreover, the solution-based proteomics revealed and confirmed the presence of several hydrolases, oxidoreductases, proteases, Kunitz-like polypeptides, and the less abundant inhibitor cysteine knot (ICK)-like (knottin) neurotoxins and insect defensin. Our results showed that the major components of the venom are toxins that are highly likely to damage cell membranes and tissue, to cause neurotoxicity, and to induce allergic reactions, thus, expanding the knowledge about venom composition and its potential biological effects on prey and victims.
蚂蚁物种具有专门的毒液系统,用于蜇刺和接种生物混合物,包括肽和多肽毒素,以进行捕食和防御。该属包括捕食性巨蚁,它们接种的毒液能够引起持久的局部疼痛、不由自主的颤抖、淋巴结病和心律失常等症状。为了更深入地了解毒液成分中的蛋白质毒素及其在化学-生态关系和人类健康中的作用,我们对俗称“假”tocandiras 的巨蚁的粗毒液进行了自下而上的蛋白质组学分析。为此,我们使用了两种不同的分析方法:(i)基于凝胶的蛋白质组学方法,其中粗毒液通过变性十二烷基硫酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)进行分离,并对所有蛋白条带进行切割分析;(ii)基于溶液的蛋白质组学方法,其中粗毒液中的蛋白质成分直接在溶液中被碎裂成胰蛋白酶肽进行分析。这两种方法得到的蛋白质组学数据与之前注释的转录组数据库进行了比较,随后对所有鉴定的转录产物进行了同源性搜索。基于凝胶的蛋白质组学方法明确鉴定出毒液中 9 种高分子质量毒素,例如酶[透明质酸酶、磷脂酶 A1、二肽基肽酶和葡萄糖脱氢酶/黄素腺嘌呤二核苷酸(FAD)醌]和多种毒液过敏原(红火蚁同源物)和毒液相关蛋白(蜂王浆样主要)。此外,基于溶液的蛋白质组学还揭示并证实了几种水解酶、氧化还原酶、蛋白酶、Kunitz 样多肽以及较少丰度的抑制剂半胱氨酸结(ICK)样(knottin)神经毒素和昆虫防御素的存在。我们的结果表明,毒液的主要成分是毒素,这些毒素很可能破坏细胞膜和组织,引起神经毒性,并引发过敏反应,从而扩大了关于毒液成分及其对猎物和受害者潜在生物学影响的知识。