Tonella L, Walsh B J, Sanchez J C, Ou K, Wilkins M R, Tyler M, Frutiger S, Gooley A A, Pescaru I, Appel R D, Yan J X, Bairoch A, Hoogland C, Morch F S, Hughes G J, Williams K L, Hochstrasser D F
Clinical Chemistry Laboratory, Geneva University Hospital, Switzerland.
Electrophoresis. 1998 Aug;19(11):1960-71. doi: 10.1002/elps.1150191114.
The combination of two-dimensional polyacrylamide gel electrophoresis (2-D PAGE), computer image analysis and several protein identification techniques allowed the Escherichia coli SWISS-2DPAGE database to be established. This is part of the ExPASy molecular biology server accessible through the WWW at the URL address http://www.expasy.ch/ch2d/ch2d-top.html . Here we report recent progress in the development of the E. coli SWISS-2DPAGE database. Proteins were separated with immobilized pH gradients in the first dimension and sodium dodecyl sulfate-polyacrylamide gel electrophoresis in the second dimension. To increase the resolution of the separation and thus the number of identified proteins, a variety of wide and narrow range immobilized pH gradients were used in the first dimension. Micropreparative gels were electroblotted onto polyvinylidene difluoride membranes and spots were visualized by amido black staining. Protein identification techniques such as amino acid composition analysis, gel comparison and microsequencing were used, as well as a recently described Edman "sequence tag" approach. Some of the above identification techniques were coupled with database searching tools. Currently 231 polypeptides are identified on the E. coli SWISS-2DPAGE map: 64 have been identified by N-terminal microsequencing, 39 by amino acid composition, and 82 by sequence tag. Of 153 proteins putatively identified by gel comparison, 65 have been confirmed. Many proteins have been identified using more than one technique. Faster progress in the E. coli proteome project will now be possible with advances in biochemical methodology and with the completion of the entire E. coli genome.
二维聚丙烯酰胺凝胶电泳(2-D PAGE)、计算机图像分析和多种蛋白质鉴定技术相结合,使得大肠杆菌SWISS-2DPAGE数据库得以建立。这是ExPASy分子生物学服务器的一部分,可通过网址http://www.expasy.ch/ch2d/ch2d-top.html在万维网上访问。在此我们报告大肠杆菌SWISS-2DPAGE数据库开发的最新进展。蛋白质在第一维通过固定化pH梯度进行分离,在第二维通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳进行分离。为了提高分离分辨率从而增加已鉴定蛋白质的数量,在第一维使用了各种宽范围和窄范围的固定化pH梯度。微量制备凝胶被电转移到聚偏二氟乙烯膜上,斑点通过酰胺黑染色进行可视化。使用了诸如氨基酸组成分析、凝胶比较和微量测序等蛋白质鉴定技术,以及最近描述的埃德曼“序列标签”方法。上述一些鉴定技术与数据库搜索工具相结合。目前在大肠杆菌SWISS-2DPAGE图谱上已鉴定出231种多肽:64种通过N端微量测序鉴定,39种通过氨基酸组成鉴定,82种通过序列标签鉴定。在通过凝胶比较推测鉴定出的153种蛋白质中,65种已得到确认。许多蛋白质使用了不止一种技术进行鉴定。随着生化方法的进步以及整个大肠杆菌基因组测序的完成,大肠杆菌蛋白质组计划现在将有可能取得更快的进展。