Lant Benjamin, Derry W Brent
Developmental and Stem Cell Biology Program, The Hospital for Sick Children, Toronto, Ontario M5G 1L7, Canada.
Cold Spring Harb Protoc. 2014 May 1;2014(5):pdb.prot080242. doi: 10.1101/pdb.prot080242.
The transparency of Caenorhabditis elegans makes it an ideal organism for visualizing proteins by immunofluorescence microscopy; however, the tough cuticle of worms and the egg shell surrounding embryos pose challenges in achieving effective fixation so that antibodies can diffuse into cells. In this protocol, we describe immunostaining of apoptosis-related proteins in the C. elegans adult germline using fluorescent reagents. Protein localization and abundance can be determined in various mutant backgrounds and under a variety of conditions, such as exposure to genotoxic stress. The number of antibodies specific to C. elegans proteins is quite limited compared with other organisms, but there is a growing list of immunological reagents directed against proteins in other organisms that cross-react with the homologous C. elegans proteins.
秀丽隐杆线虫的透明性使其成为通过免疫荧光显微镜观察蛋白质的理想生物体;然而,线虫坚硬的角质层和胚胎周围的卵壳对实现有效的固定提出了挑战,以便抗体能够扩散到细胞中。在本实验方案中,我们描述了使用荧光试剂对秀丽隐杆线虫成年生殖系中凋亡相关蛋白进行免疫染色的方法。可以在各种突变背景下以及在多种条件下,如暴露于基因毒性应激下,确定蛋白质的定位和丰度。与其他生物体相比,针对秀丽隐杆线虫蛋白质的特异性抗体数量相当有限,但针对其他生物体中与秀丽隐杆线虫同源蛋白质发生交叉反应的蛋白质的免疫试剂清单正在不断增加。