Ferullo J M, Nespoulous L
Département de Physiologie Végétale et Ecosystèmes, Centre d'Etudes Nucléaires de Cadarache, St. Paul-lez-Durance, France.
Anal Biochem. 1991 Oct;198(1):131-3. doi: 10.1016/0003-2697(91)90516-v.
We have adapted a two-dimensional electrophoretic technique described by P. Z. O'Farrell et al. (Cell 12, 1133-1142, 1977) to Phastsystem, resolving both acidic and basic proteins by using nonequilibrium pH gradient electrophoresis in the first dimension and sodium dodecyl sulfate polyacrylamide gel electrophoresis in the second dimension. Protein separation was optimized for the analysis of plant proteins. The use of the Phastsystem apparatus reduced times of preparation and separation, allowing the rapid screening of plant proteins on a large scale of isoelectric points. This technique was used for the immunodetection and characterization of two stress-induced proteins in irradiated tomato leaves.
我们采用了P.Z.奥法雷尔等人(《细胞》12卷,1133 - 1142页,1977年)描述的二维电泳技术,将其应用于Phastsystem系统,通过在第一维使用非平衡pH梯度电泳以及在第二维使用十二烷基硫酸钠聚丙烯酰胺凝胶电泳来分离酸性和碱性蛋白质。针对植物蛋白质分析对蛋白质分离进行了优化。Phastsystem仪器的使用减少了制备和分离时间,能够对植物蛋白质的等电点进行大规模快速筛选。该技术用于对辐照番茄叶片中两种胁迫诱导蛋白进行免疫检测和特性鉴定。