Hird H, Pumphrey R, Wilson P, Sunderland J, Reece P
Central Science Laboratory, Sand Hutton, York, UK.
Electrophoresis. 2000 Jul;21(13):2678-83. doi: 10.1002/1522-2683(20000701)21:13<2678::AID-ELPS2678>3.0.CO;2-V.
A procedure for the native two-dimensional electrophoresis of peanut and hazelnut proteins is described. Proteins were solubilised after acetone treatment using a combination of 3-[(3-cholamidopropyl)dimethylammonio]-1-propanesulfonate (CHAPS) and tetramethylene sulphone. These extracts were analysed by a combination of isoelectric focusing in the presence of lactose in immobilized pH gradients followed by charge shift electrophoresis. Immunoblot analysis, using sera from nut allergic patients, allowed the identification of a peanut and hazelnut allergen with identical isoelectric point and apparent molecular mass. These proteins were recovered from duplicate gels using a mixture of formic acid, acetonitrile (ACN) and isopropanol. The molecular masses for both proteins, determined by matrix assisted laser desorption/ionisation-mass spectrometry (MALDI-MS), were 4826 Da.
本文描述了一种用于花生和榛子蛋白的天然二维电泳方法。使用3-[(3-胆酰胺丙基)二甲基铵]-1-丙烷磺酸盐(CHAPS)和四亚甲基砜的组合在丙酮处理后溶解蛋白质。这些提取物通过在固定pH梯度中存在乳糖的等电聚焦,然后进行电荷转移电泳进行分析。使用坚果过敏患者的血清进行免疫印迹分析,鉴定出具有相同等电点和表观分子量的花生和榛子过敏原。使用甲酸、乙腈(ACN)和异丙醇的混合物从重复的凝胶中回收这些蛋白质。通过基质辅助激光解吸/电离质谱(MALDI-MS)测定的两种蛋白质的分子量均为4826 Da。