Ducancel Frédéric, Durban Jordi, Verdenaud Marion
Department of ImmunoVirology, iMETI/DSV/CEA, Bt 02, 18 rue du Panorama, BP 6, 92265, Fontenay-aux-Roses, France.
Future Med Chem. 2014 Oct;6(15):1629-43. doi: 10.4155/fmc.14.95.
Over the last three decades, transcriptomic studies of venom gland cells have continuously evolved, opening up new possibilities for exploring the molecular diversity of animal venoms, a prerequisite for the discovery of new drug candidates and molecular phylogenetics. The molecular complexity of animal venoms is much greater than initially thought. In this review, we describe the different technologies available for transcriptomic studies of venom, from the original individual cloning approaches to the more recent global Next Generation Sequencing strategies. Our understanding of animal venoms is evolving, with the discovery of complex and diverse bio-optimized cocktails of compounds, including mostly peptides and proteins, which are now beginning to be studied by academic and industrial researchers.
在过去三十年中,毒腺细胞的转录组学研究不断发展,为探索动物毒液的分子多样性开辟了新的可能性,这是发现新候选药物和进行分子系统发育研究的先决条件。动物毒液的分子复杂性比最初想象的要大得多。在这篇综述中,我们描述了可用于毒液转录组学研究的不同技术,从最初的个体克隆方法到最近的全局下一代测序策略。随着复杂多样的生物优化化合物混合物(主要包括肽和蛋白质)的发现,我们对动物毒液的理解正在不断演变,目前学术和工业研究人员已开始对其进行研究。