Jahnen W, Ward L D, Reid G E, Moritz R L, Simpson R J
Joint Protein Structure Laboratory, Ludwig Institute for Cancer Research, (Melbourne Branch), Parkville, Victoria, Australia.
Biochem Biophys Res Commun. 1990 Jan 15;166(1):139-45. doi: 10.1016/0006-291x(90)91922-f.
A new method was developed for generating peptide fragments for amino acid sequence analysis from polyacrylamide-gel separated proteins. This method involves in situ CNBr treatment of proteins in the polyacrylamide gel after their separation by electrophoresis. Pure CNBr peptides were recovered either by solvent extraction followed by microbore column reversed-phase HPLC or, alternatively, by a second electrophoretic separation step (SDS-PAGE) followed by electrotransfer of the peptides onto polyvinylidene difluoride (PVDF) membranes. These approaches yielded sequence data at subnanomole levels for a wide range of CNBr fragments recovered from gel-separated proteins.
开发了一种新方法,用于从聚丙烯酰胺凝胶分离的蛋白质中生成用于氨基酸序列分析的肽片段。该方法包括在通过电泳分离聚丙烯酰胺凝胶中的蛋白质后,对其进行原位溴化氰(CNBr)处理。通过溶剂萃取后进行微径柱反相高效液相色谱法(HPLC),或者通过第二步电泳分离步骤(SDS-PAGE),然后将肽电转移到聚偏二氟乙烯(PVDF)膜上,来回收纯的CNBr肽。这些方法为从凝胶分离的蛋白质中回收的各种CNBr片段提供了亚纳摩尔水平的序列数据。