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利用串联质谱中固有的同位素信息改进肽测序。

Improved peptide sequencing using isotope information inherent in tandem mass spectra.

作者信息

Cannon William R, Jarman Kenneth D

机构信息

Computational Biosciences, Pacific Northwest National Laboratory, Richland, WA 99352, USA.

出版信息

Rapid Commun Mass Spectrom. 2003;17(15):1793-801. doi: 10.1002/rcm.1119.

Abstract

We demonstrate here the use of natural isotopic 'labels' in peptides to aid in the identification of peptides with a de novo algorithm. Using data from ion trap tandem mass spectrometric (MS/MS) analysis of 102 tryptic peptides, we have analyzed multiple series of peaks within LCQ MS/MS spectra that 'spell' peptide sequences. Isotopic peaks from naturally abundant isotopes are particularly prominent even after peak centroiding on y- and b-series ions and lead to increased confidence in the identification of the precursor peptides. Sequence analysis of the MS/MS data is accomplished by finding sequences and subsequences in a hierarchical manner within the spectra.

摘要

我们在此展示了在肽中使用天然同位素“标签”,以借助从头算法来鉴定肽。利用来自102个胰蛋白酶肽的离子阱串联质谱(MS/MS)分析的数据,我们分析了LCQ MS/MS谱内多个系列的峰,这些峰“拼出”了肽序列。即使在对y系列和b系列离子进行峰中心定位之后,来自天然丰度同位素的同位素峰仍然特别突出,并提高了对前体肽鉴定的可信度。MS/MS数据的序列分析是通过在谱内以分层方式找到序列和子序列来完成的。

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