Pandey S, Parnaik V K
Centre for Cellular and Molecular Biology, Hyderabad, India.
Biochem J. 1989 Aug 1;261(3):733-8. doi: 10.1042/bj2610733.
A sensitive technique is described for the rapid identification of nuclear-envelope proteins. Mouse liver nuclei (purified on sucrose gradients) were iodinated with Na125I by the immobilized water-insoluble reagent Iodogen. Iodinated nuclei were digested with RNAase A and DNAase I and then salt-extracted to obtain labelled nuclear envelopes. Nuclear envelopes were characterized by morphological and biochemical criteria and by SDS/polyacrylamide-gel electrophoresis. In all, 13 polypeptides of molecular masses 145, 115, 98, 85, 75, 70, 65, 54, 50, 45, 40, 38 and 36 kDa were identified in the labelled nuclear envelopes. The labelled polypeptides were localized to the nuclear envelope by extraction of the envelope with Triton X-100 and different concentrations of salt. Iodination of intact nuclei was shown to be specific for the nuclear envelope by the absence of labelling of histones and cytoplasmic contaminants.
本文描述了一种用于快速鉴定核膜蛋白的灵敏技术。通过固定化水不溶性试剂碘甘醚,用Na125I对经蔗糖梯度纯化的小鼠肝细胞核进行碘化。碘化的细胞核用核糖核酸酶A和脱氧核糖核酸酶I消化,然后用盐提取以获得标记的核膜。通过形态学、生化标准以及SDS/聚丙烯酰胺凝胶电泳对核膜进行表征。总共在标记的核膜中鉴定出13种分子量分别为145、115、98、85、75、70、65、54、50、45、40、38和36 kDa的多肽。通过用Triton X-100和不同浓度的盐提取核膜,将标记的多肽定位到核膜上。由于组蛋白和细胞质污染物未被标记,完整细胞核的碘化显示出对核膜具有特异性。