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Identification of the Components of Simple Protein Mixtures by High-Accuracy Peptide Mass Mapping and Database Searching

机译:高精度肽质谱图和数据库搜索鉴定简单蛋白质混合物的成分

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摘要

Peptide mass mapping by matrix-assisted laser desorption/ionization (MALD1) 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.
机译:现在,通过基质辅助激光解吸/电离(MALD1)进行肽质量映射,然后使用一组测得的肽质量进行数据库搜索,是鉴定纯蛋白质的有效方法。迄今为止,蛋白质混合物(例如由于聚丙烯酰胺凝胶带迁移而经常发生)迄今仍需要进行蛋白质测序。在这里,我们证明了这种蛋白质条带也可以通过单独的肽质量图分析。通过延迟萃取MALDI质谱法测定的肽质量完整列表的数据库搜索,质量误差小于30 ppm,可检索混合物中最突出的蛋白质。在第二步中,通过使尽可能多的测得的肽质量与检索到的氨基酸序列相匹配,进一步确定蛋白质同一性。再次搜索“第二遍搜索”后剩余的肽质量,以鉴定蛋白质混合物中的下一个成分。重复此迭代过程,直到考虑到所有主要离子信号为止。可以分析由单个凝胶带中的两个或多个单独成分组成的蛋白质混合物,从而进一步提高了MALDI肽图谱用于蛋白质鉴定的一般适用性。

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