Leffers H, Dejgaard K, Honoré B, Madsen P, Nielsen M S, Celis J E
Institute of Medical Biochemistry, Aarhus University, Denmark.
Electrophoresis. 1996 Nov;17(11):1713-9. doi: 10.1002/elps.1150171108.
The rapid progress in characterizing genes and mRNAs (expressed sequence tags, ESTs) as a result of the Human Genome Project makes it imperative to develop strategies to interface DNA mapping and sequencing data with protein information, as the latter orchestrate most cellular functions. Presently, the only technique able to resolve and record the thousands of proteins present in cells and tissues is two-dimensional (2-D) gel electrophoresis in combination with computer-aided technology to scan the gels, make synthetic images, assign numbers to individual spots as well as to enter qualitative and quantitative information. To date, comprehensive 2-D gel databases containing information about various properties of proteins (cellular localization, identification, regulatory properties, partial amino acid sequences, etc.) have been established (available on the internet: http:@biobase.dk/cgi-bin/celis). What remains is to provide a link between these data and the forthcoming information from the Human Genome Project. We are pursuing two approaches to achieve this goal: (i) microsequencing and mass spectrometry analysis of proteins resolved from 2-D gels and (ii) expression of cDNAs in the vaccinia virus expression system. Using the latter approach we have expressed about 60 cDNAs in human cells under conditions that faithfully reproduce post-translational trimmings and modifications of the proteins. The method, in combination with 2-D gel electrophoresis, allows precise matching of almost any cDNA to its protein product, irrespective of the protein abundance.
人类基因组计划使得在基因和mRNA(表达序列标签,ESTs)特性描述方面取得了快速进展,这就迫切需要开发一些策略,将DNA图谱和测序数据与蛋白质信息联系起来,因为蛋白质调控着大多数细胞功能。目前,唯一能够分辨并记录细胞和组织中数千种蛋白质的技术是二维(2-D)凝胶电泳,它与计算机辅助技术相结合,用于扫描凝胶、制作合成图像、为各个斑点编号以及输入定性和定量信息。到目前为止,已经建立了包含蛋白质各种特性(细胞定位、鉴定、调控特性、部分氨基酸序列等)信息的全面的二维凝胶数据库(可在互联网上获取:http:@biobase.dk/cgi-bin/celis)。剩下的就是要在这些数据与人类基因组计划即将产生的信息之间建立联系。我们正在通过两种方法来实现这一目标:(i)对二维凝胶上分离出的蛋白质进行微量测序和质谱分析,以及(ii)在痘苗病毒表达系统中表达cDNA。使用后一种方法,我们已经在人类细胞中表达了约60种cDNA,这些条件能够忠实地重现蛋白质的翻译后修饰和加工。该方法与二维凝胶电泳相结合,几乎可以将任何cDNA与其蛋白质产物精确匹配,而不考虑蛋白质的丰度。