Hailat N Q, Hanash S M
Molecular Pathology Laboratory, Jordan University of Science & Technology, Irbid.
Indian J Biochem Biophys. 1995 Oct;32(5):240-4.
A major effort of our work has been devoted to the identification, using two-dimensional polyacrylamide gel electrophoresis (2-D PAGE), of lymphoid polypeptides that are involved in lymphoid proliferation or differentiation. We have encountered problems during this effort pertaining to the exact localization of a polypeptide(s) in the silver stained gels that is recognized by western immunoblotting or proteins detected by autoradiography. In this paper, we present a method, using India ink stained/immuno-staining replica of 2-D gel nitrocellulose membrane (NCM) or India ink stained coupled with autoradiography in the case of phosphoproteins, which allows us to exactly localize the polypeptide spots detected by these methods in the silver stained 2-D PAGE. This method is expected to popularize and widen the use of 2-D PAGE technology in the investigation of cellular polypeptides.
我们工作的一项主要努力致力于通过二维聚丙烯酰胺凝胶电泳(2-D PAGE)鉴定参与淋巴细胞增殖或分化的淋巴样多肽。在这项工作中,我们遇到了一些问题,涉及通过蛋白质免疫印迹法识别的多肽在银染凝胶中的准确定位,或通过放射自显影检测的蛋白质的定位。在本文中,我们提出了一种方法,对于磷酸化蛋白,使用二维凝胶硝酸纤维素膜(NCM)的印度墨水染色/免疫染色复制品,或印度墨水染色结合放射自显影,这使我们能够在银染的二维PAGE中准确定位通过这些方法检测到的多肽斑点。预计该方法将推广并扩大二维PAGE技术在细胞多肽研究中的应用。