Jensen O N, Podtelejnikov A V, Mann M
Protein & Peptide Group, European Molecular Biology Laboratory (EMBL), Heidelberg, Germany.
Anal Chem. 1997 Dec 1;69(23):4741-50. doi: 10.1021/ac970896z.
Peptide mass mapping by matrix-assisted laser desorption/ionization (MALDI) followed by database searching with the set of measured peptide masses is now a powerful method for the identification of pure proteins. Protein mixtures--such as frequently occur due to comigration in polyacrylamide gel bands--have hitherto required protein sequencing. Here we demonstrate that such protein bands can also be analyzed by peptide mass mapping alone. Database searching with the complete list of peptide masses determined by delayed-extraction MALDI mass spectrometry with a mass error of less than 30 ppm retrieves the most prominent protein in a mixture. In a second step, the protein identity is further confirmed by matching as many of the measured peptide masses as possible to the retrieved amino acid sequence. Peptide masses remaining after this "second pass search" are searched again to identify the next component in the protein mixture. This iterative process is repeated until all major ion signals are accounted for. Protein mixtures consisting of two or more individual components in a single gel band can be analyzed, further increasing the general applicability of MALDI peptide mapping for protein identification.
通过基质辅助激光解吸/电离(MALDI)进行肽质量图谱分析,然后用测得的肽质量集进行数据库搜索,现在是鉴定纯蛋白质的一种强大方法。蛋白质混合物——例如由于在聚丙烯酰胺凝胶条带中共迁移而经常出现的混合物——迄今为止需要进行蛋白质测序。在这里,我们证明此类蛋白质条带也可以仅通过肽质量图谱分析来进行分析。使用延迟提取MALDI质谱法测定的肽质量完整列表进行数据库搜索,质量误差小于30 ppm,可检索混合物中最主要的蛋白质。第二步,通过将尽可能多的测得肽质量与检索到的氨基酸序列进行匹配,进一步确认蛋白质的身份。在这次“二次搜索”后剩余的肽质量再次进行搜索,以鉴定蛋白质混合物中的下一个成分。重复这个迭代过程,直到所有主要离子信号都得到解释。可以分析在单个凝胶条带中由两个或更多个单独成分组成的蛋白质混合物,进一步提高了MALDI肽图谱用于蛋白质鉴定的普遍适用性。