Luo Haitao, Rankin Gary O, Straley Shannon, Chen Yi Charlie
Natural Science Division, Alderson-Broaddus College, Philippi, WV 26416, USA.
J Pharmacol Toxicol Methods. 2011 Nov-Dec;64(3):233-7. doi: 10.1016/j.vascn.2011.06.001. Epub 2011 Jun 30.
Western blotting is a basic technique for protein detection. For proteins of less abundance or antibodies of poorer quality, an increased sensitivity is often desired. Although it is commonly known that higher concentrations of antibodies and prolonged film exposure times will help improve sensitivity in western blots, both measures come with their own risks, and it is often unclear to which extent these measures should be applied.
We conducted time-course studies to investigate protein-antibody interactions and primary antibody-secondary antibody interactions in western blotting. We also propose a protocol of stacked film exposure and have tested it in standard curves and cancer cell samples.
Our study found that protein-primary antibody interactions and primary antibody-secondary antibody interactions could take a longer time than commonly used "one hour" or "overnight", and in some cases longer than 48h, to reach its maximum binding. We also show that the modified protocol of stacked film exposure works well for both standard curves and biological samples, reaching a maximum sensitivity in western blots without blurring target signals or increasing backgrounds.
In addition to regular optimization of antibody concentrations and film exposure time, a prolonged incubation with antibodies and stacked film exposure will also help improve sensitivity and reduce background in western blotting.
蛋白质印迹法是蛋白质检测的一项基本技术。对于丰度较低的蛋白质或质量较差的抗体,通常需要提高检测灵敏度。虽然众所周知,在蛋白质印迹法中使用更高浓度的抗体和延长胶片曝光时间有助于提高灵敏度,但这两种方法都有各自的风险,而且通常不清楚这些方法应应用到何种程度。
我们进行了时间进程研究,以调查蛋白质印迹法中蛋白质与抗体的相互作用以及一抗与二抗的相互作用。我们还提出了一种叠加胶片曝光方案,并在标准曲线和癌细胞样本中进行了测试。
我们的研究发现,蛋白质与一抗的相互作用以及一抗与二抗的相互作用可能比常用的“一小时”或“过夜”时间更长,在某些情况下超过48小时才能达到最大结合。我们还表明,改进后的叠加胶片曝光方案在标准曲线和生物样本中均效果良好,在蛋白质印迹法中可达到最大灵敏度,而不会使目标信号模糊或增加背景。
除了常规优化抗体浓度和胶片曝光时间外,延长抗体孵育时间和叠加胶片曝光也有助于提高蛋白质印迹法的灵敏度并减少背景。