Kurien Biji T, Scofield R Hal
Oklahoma Medical Research Foundation, 825 NE 13th Street, OKC, OK, 73104, USA.
Methods Mol Biol. 2009;536:181-90. doi: 10.1007/978-1-59745-542-8_20.
An ultrarapid method for the electrophoretic transfer of high and low molecular weight proteins to nitrocellulose membranes following sodium dodecyl sulfate (SDS) polyacrylamide gel is described here. The transfer was performed with heated (70-75 degrees C) normal transfer buffer from which methanol had been omitted. Complete transfer of high and low molecular weight antigens (molecular weight protein standards, a purified protein, and proteins from a human tissue extract) could be carried out in 10 min for a 7% (0.75 mm) SDS polyacrylamide gel. For 10 and 12.5% gels (0.75 mm) the corresponding time was 15 min. A complete transfer could be carried out in 20 min for 7, 10, and 12.5% gels (1.5 mm gels). The permeability of the gel is increased by heat, such that the proteins trapped in the polyacrylamide gel matrix can be easily transferred to the membrane. The heat mediated transfer method was compared with a conventional transfer protocol, under similar conditions. The conventional method transferred minimal low molecular weight proteins while retaining most of the high molecular weight proteins in the gel. In summary, this procedure is particularly useful for the transfer of high molecular weight proteins, very rapid, and avoids the use of methanol.
本文描述了一种超快速方法,用于在十二烷基硫酸钠(SDS)聚丙烯酰胺凝胶电泳后,将高分子量和低分子量蛋白质电泳转移至硝酸纤维素膜上。转移过程使用加热至70 - 75摄氏度的正常转移缓冲液,其中已省略甲醇。对于7%(0.75毫米)的SDS聚丙烯酰胺凝胶,高分子量和低分子量抗原(分子量蛋白质标准品、一种纯化蛋白质以及来自人体组织提取物的蛋白质)可在10分钟内完全转移。对于10%和12.5%的凝胶(0.75毫米),相应时间为15分钟。对于7%、10%和12.5%的凝胶(1.5毫米凝胶),20分钟内可完成完全转移。加热可增加凝胶的通透性,使得被困在聚丙烯酰胺凝胶基质中的蛋白质能够轻松转移至膜上。在相似条件下,将热介导转移方法与传统转移方案进行了比较。传统方法转移的低分子量蛋白质极少,同时大部分高分子量蛋白质保留在凝胶中。总之,该方法对于高分子量蛋白质的转移特别有用,速度非常快,并且避免了使用甲醇。