Department of Chemistry, University of Michigan, Ann Arbor, Michigan 48109, USA.
Anal Chem. 2011 Feb 15;83(4):1350-5. doi: 10.1021/ac102671n. Epub 2011 Jan 25.
A microscale Western blotting system based on separating sodium-dodecyl sulfate protein complexes by capillary gel electrophoresis followed by deposition onto a blotting membrane for immunoassay is described. In the system, the separation capillary is grounded through a sheath capillary to a mobile X-Y translation stage which moves a blotting membrane past the capillary outlet for protein deposition. The blotting membrane is moistened with a methanol and buffer mixture to facilitate protein adsorption. Although discrete protein zones could be detected, bands were broadened by ∼1.7-fold by transfer to membrane. A complete Western blot for lysozyme was completed in about one hour with 50 pg mass detection limit from low microgram per milliliter samples. These results demonstrate substantial reduction in time requirements and improvement in mass sensitivity compared to conventional Western blots. Western blotting using capillary electrophoresis shows promise to analyze low volume samples with reduced reagents and time, while retaining the information content of a typical Western blot.
一种基于毛细管凝胶电泳分离十二烷基硫酸钠蛋白复合物,然后将其沉积到印迹膜上进行免疫检测的微尺度 Western 印迹系统。在该系统中,分离毛细管通过鞘毛细管接地到一个可移动的 X-Y 平移台上,该平移台将印迹膜移动到毛细管出口以进行蛋白质沉积。印迹膜用甲醇和缓冲液混合物润湿,以促进蛋白质吸附。尽管可以检测到离散的蛋白质区带,但通过转移到膜上,条带的宽度扩大了约 1.7 倍。从低微克/毫升的样品中,用 50pg 质量检测下限,约一小时内完成了溶菌酶的完整 Western 印迹。与传统的 Western 印迹相比,这些结果表明时间要求大大减少,质量灵敏度提高。毛细管电泳的 Western 印迹有望分析低体积样品,减少试剂和时间,同时保留典型 Western 印迹的信息含量。