Escoubas Pierre, Corzo Gerardo, Whiteley Brian J, Célérier Marie-Louise, Nakajima Terumi
Suntory Institute for Bioorganic Research, Mishima-Gun, Shimamoto-Cho, Wakayamadai 1-1-1, Osaka 618-8503, Japan.
Rapid Commun Mass Spectrom. 2002;16(5):403-13. doi: 10.1002/rcm.595.
Animal venoms are important sources of novel pharmacological tools, useful in biochemical characterization of their receptors. Venom quality control, batch-to-batch homogeneity and high reproducibility of venom fractionation and toxin purification are crucial issues for biochemical and pharmacological studies. To address these issues, a study of the variability of tarantula spider venom samples was undertaken. Venom profiles of samples collected from individuals of different age and sex, and from sibling spiders of the same species, were generated by high-performance liquid chromatography (HPLC) and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOFMS) and analyzed to assess venom variability and method accuracy. Sex-linked venom variation was studied on eight species. Clear qualitative differences were observed for six out of eight species, as well as quantitative differences. Age-related variation studied in Poecilotheria rufilata showed essentially age-related quantitative differences between adults of both sexes and immature juveniles. The venoms of nine siblings and three wild-collected Pterinochilus murinus were studied for individual variation, showing only very minor quantitative differences. On the same samples, the quality of MALDI-TOFMS venom fingerprinting was demonstrated to be highly reproducible. Our results show that tarantula venom peptide fingerprinting is a highly reliable identification method, that pooled batches of venom from several animals can be used for venom purification, that venom composition does not appear to be qualitatively related to ontogenesis in the spiders studied, and that qualitative sex-linked variation occurs across most species and may be important in activity studies.
动物毒液是新型药理学工具的重要来源,有助于对其受体进行生化特性分析。毒液的质量控制、批次间的均一性以及毒液分级分离和毒素纯化的高重现性是生化和药理学研究的关键问题。为解决这些问题,我们对狼蛛毒液样本的变异性进行了研究。通过高效液相色谱法(HPLC)和基质辅助激光解吸/电离飞行时间质谱法(MALDI-TOFMS)生成了从不同年龄和性别的个体以及同一物种的同胞蜘蛛采集的样本的毒液图谱,并进行分析以评估毒液变异性和方法准确性。对八个物种研究了与性别相关的毒液变异。在八个物种中的六个物种中观察到了明显的定性差异以及定量差异。对红斑寇蛛进行的与年龄相关的变异研究表明,成年雌雄个体和未成熟幼体之间基本上存在与年龄相关的定量差异。对九只同胞蜘蛛和三只野生采集的穆氏啸蛛的毒液进行了个体变异研究,结果仅显示出非常微小的定量差异。对于相同的样本,MALDI-TOFMS毒液指纹图谱的质量被证明具有高度重现性。我们的结果表明,狼蛛毒液肽指纹图谱是一种高度可靠的鉴定方法,可以使用从几只动物收集的混合毒液批次进行毒液纯化,在所研究的蜘蛛中,毒液成分在定性上似乎与个体发育无关,并且定性的与性别相关的变异在大多数物种中都存在,并且可能在活性研究中很重要。