Pallen Catherine, Friry-Santini Claire, Herouet-Guicheney Corinne, Capt Annabelle
Bayer SAS, Bayer CropScience, Research Toxicology, Sophia Antipolis, France.
Toxicol Rep. 2014 Sep 16;1:734-742. doi: 10.1016/j.toxrep.2014.09.002. eCollection 2014.
Two-dimensional gel electrophoresis (2-DE) technique is used as a performing technique to assess the variability of protein expression in crops, and especially soybean endogenous food allergens, which are a subset of proteins of interest for assessing whether genetically modified (GM) soybean has a different allergenic profile compared to its non-GM counterpart. On top of the biological variability of the 2-DE, which has already been studied by several laboratories, technical variability has to be evaluated. In this study, several sources of variability (number of gel replicates, protein extracts, study timings and operators) were assessed qualitatively and quantitatively on all detectable polypeptide spots as well as on food allergen spots. Results showed that the major source of variability was the number of gel replicates. Other sources were minor. This has a direct practical impact on the laboratory work as this supports the utilization of three or four gel replicates to get robust results. Furthermore, this implies that the study can be run over several days, and be performed by several trained operators, without impacting its reproducibility. Furthermore, 2-DE could detect a 2-fold change between two samples with an acceptable rate of false positives (below 7%). This level of sensitivity is acceptable in the context of safety assessment of GM soybean as the biological variability of proteins in soybean is higher than the technical variability shown in this study. Overall, the 2-DE technique is suitable for investigating endogenous food allergen variability between several soybean seeds, including GM and non-GM counterpart.
二维凝胶电泳(2-DE)技术被用作一种分析技术,以评估作物中蛋白质表达的变异性,特别是大豆内源性食物过敏原,这些过敏原是蛋白质的一个子集,用于评估转基因(GM)大豆与其非转基因对应物相比是否具有不同的过敏特性。除了几个实验室已经研究过的2-DE的生物学变异性之外,还必须评估技术变异性。在本研究中,对所有可检测的多肽斑点以及食物过敏原斑点,定性和定量地评估了几个变异性来源(凝胶重复次数、蛋白质提取物、研究时间和操作人员)。结果表明,变异性的主要来源是凝胶重复次数。其他来源的影响较小。这对实验室工作有直接的实际影响,因为这支持使用三到四次凝胶重复来获得可靠的结果。此外,这意味着该研究可以在几天内进行,并且由几位经过培训的操作人员完成,而不会影响其可重复性。此外,2-DE能够在假阳性率可接受(低于7%)的情况下检测到两个样品之间2倍的变化。在转基因大豆安全性评估的背景下,这种灵敏度水平是可以接受的,因为大豆中蛋白质的生物学变异性高于本研究中显示的技术变异性。总体而言,2-DE技术适用于研究几种大豆种子(包括转基因和非转基因对应物)之间的内源性食物过敏原变异性。