Wilkins M R, Ou K, Appel R D, Sanchez J C, Yan J X, Golaz O, Farnsworth V, Cartier P, Hochstrasser D F, Williams K L, Gooley A A
Macquarie University Centre for Analytical Biotechnology, Sydney, New South Wales, Australia.
Biochem Biophys Res Commun. 1996 Apr 25;221(3):609-13. doi: 10.1006/bbrc.1996.0643.
Proteins can be identified by amino acid analysis and database matching, but it is often desirable to increase the confidence in identity through the use of other techniques. Here we describe a rapid protein identification method that uses Edman degradation to create a 3 or 4 amino acid N-terminal "sequence tag," following which proteins are subjected to amino acid analysis protein identification procedures. Edman degradation methods have been modified to take only 23 min per cycle, and rapid amino acid analysis techniques are used. The Edman degradation and amino acid analysis is done on a single PVDF membrane-bound protein sample. A computer database matching program is also presented which uses both amino acid composition and "sequence tag" data for protein identification. This method represents the most inexpensive, accurate, and rapid means of protein identification, which is ideal for the screening of proteomes separated by 2-D gel electrophoresis. The creation of N-terminal Edman degradation "sequence-tags" prior to peptide mass fingerprinting of samples should also be useful.
蛋白质可通过氨基酸分析和数据库匹配来鉴定,但通常希望通过使用其他技术来提高鉴定的可信度。在此,我们描述一种快速蛋白质鉴定方法,该方法利用埃德曼降解法生成一个3或4个氨基酸的N端“序列标签”,之后对蛋白质进行氨基酸分析蛋白质鉴定程序。埃德曼降解方法已被改进,每个循环仅需23分钟,并采用了快速氨基酸分析技术。埃德曼降解和氨基酸分析在单个与聚偏二氟乙烯(PVDF)膜结合的蛋白质样品上进行。还介绍了一种计算机数据库匹配程序,该程序使用氨基酸组成和“序列标签”数据进行蛋白质鉴定。此方法是最廉价、准确且快速的蛋白质鉴定手段,非常适合用于筛选通过二维凝胶电泳分离的蛋白质组。在对样品进行肽质量指纹图谱分析之前创建N端埃德曼降解“序列标签”也应会很有用。