Kaur R, Dikshit K L, Raje M
Institute of Microbial Technology, Sector 39A, Chandigarh 160036, India.
J Microsc. 2002 Nov;208(Pt 2):100-7. doi: 10.1046/j.1365-2818.2002.01072.x.
Rapid and sensitive pre-screening for the presence of antigens in cell samples and confirmation of reactivity of antibodies, before proceeding with electron microscopy, is highly desirable. Most of the methods developed for this purpose are generally not very efficient and suitable for dealing with very small volumes of sample and reagents. In this work we present a simple, sensitive and rapid solid phase transmission electron microscope (TEM) based method for the detection of picogram (pg) levels of soluble antigens using as little as 10 micro L of reagents. Protein was adsorbed onto grids coated with polystyrene films to form the solid phase. The presence of antigen was detected using immunogold labelling. Gold particles adhering to the film were visualized and counted in a TEM providing a digital signal. This method was 100-fold more sensitive than dot blot in detection of rabbit IgG. We have demonstrated the utility of this technique by screening for Vitreoscilla haemoglobin (VHb) antigen in cell lysates and confirming the results directly with immunogold labelling transmission electron microscopy of cell sections.
在进行电子显微镜检查之前,对细胞样本中的抗原进行快速灵敏的预筛选以及确认抗体的反应性是非常必要的。为此目的开发的大多数方法通常效率不高,且适合处理极少量的样本和试剂。在这项工作中,我们提出了一种基于简单、灵敏且快速的固相透射电子显微镜(TEM)的方法,用于检测皮克(pg)水平的可溶性抗原,试剂用量低至10微升。将蛋白质吸附到涂有聚苯乙烯薄膜的网格上以形成固相。使用免疫金标记检测抗原的存在。附着在薄膜上的金颗粒在透射电子显微镜下可视化并计数,从而提供数字信号。在检测兔IgG方面,该方法比斑点印迹法灵敏100倍。我们通过筛选细胞裂解物中的透明颤菌血红蛋白(VHb)抗原,并直接用细胞切片的免疫金标记透射电子显微镜确认结果,证明了该技术的实用性。