Panchout François, Letendre Julie, Bultelle Florence, Denier Xavier, Rocher Béatrice, Chan Philippe, Vaudry David, Durand Fabrice
Laboratory of Ecotoxicology-Aquatic Environments, LEMA, EA 3222, and.
J Biomol Tech. 2013 Dec;24(4):218-23. doi: 10.7171/jbt.13-2404-002.
As it is well-established that protein extraction constitutes a crucial step for two-dimensional electrophoresis (2DE), this work was done as a prerequisite to further the study of alterations in the proteome in gills of the shore crab Carcinus maenas under contrasted environmental conditions. Because of the presence of a chitin layer, shore crab gills have an unusual structure. Consequently, they are considered as a hard tissue and represent a challenge for optimal protein extraction. In this study, we compared three published extraction procedures for subsequent applications to 2DE: the first one uses homogenization process, the second one included an additional TCA-acetone precipitation step, and finally, the third one associated grinding in liquid nitrogen (N2) and TCA-acetone precipitation. Extracted proteins were then resolved using 1DE and 2DE. Although interesting patterns were obtained using 1DE with the three methods, only the one involving grinding in liquid N2 and TCA-acetone precipitation led to proper resolution after 2DE, showing a good level of reproducibility at technical (85%) and biological (84%) levels. This last method is therefore proposed for analysis of gill proteomes in the shore crab.
由于蛋白质提取是二维电泳(2DE)的关键步骤,这项工作是进一步研究在不同环境条件下岸蟹(Carcinus maenas)鳃蛋白质组变化的前提。由于存在几丁质层,岸蟹的鳃具有特殊结构。因此,它们被视为硬组织,对最佳蛋白质提取构成挑战。在本研究中,我们比较了三种已发表的用于后续2DE应用的提取方法:第一种使用匀浆过程,第二种包括额外的三氯乙酸-丙酮沉淀步骤,最后,第三种结合液氮(N2)研磨和三氯乙酸-丙酮沉淀。然后使用一维电泳(1DE)和二维电泳(2DE)分离提取的蛋白质。尽管使用这三种方法通过1DE获得了有趣的图谱,但只有涉及液氮研磨和三氯乙酸-丙酮沉淀的方法在2DE后能得到适当的分辨率,在技术(85%)和生物学(84%)水平上显示出良好的重现性。因此,建议使用最后这种方法对岸蟹鳃蛋白质组进行分析。