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利用肽段可检测性从鸟枪法蛋白质组学进行蛋白质推断的进展。

Advancement in protein inference from shotgun proteomics using peptide detectability.

作者信息

Alves Pedro, Arnold Randy J, Novotny Milos V, Radivojac Predrag, Reilly James P, Tang Haixu

机构信息

School of Informatics, Indiana University, Bloomington, USA.

出版信息

Pac Symp Biocomput. 2007:409-20.

Abstract

A major challenge in shotgun proteomics has been the assignment of identified peptides to the proteins from which they originate, referred to as the protein inference problem. Redundant and homologous protein sequences present a challenge in being correctly identified, as a set of peptides may in many cases represent multiple proteins. One simple solution to this problem is the assignment of the smallest number of proteins that explains the identified peptides. However, it is not certain that a natural system should be accurately represented using this minimalist approach. In this paper, we propose a reformulation of the protein inference problem by utilizing the recently introduced concept of peptide detectability. We also propose a heuristic algorithm to solve this problem and evaluate its performance on synthetic and real proteomics data. In comparison to a greedy implementation of the minimum protein set algorithm, our solution that incorporates peptide detectability performs favorably.

摘要

鸟枪法蛋白质组学中的一个主要挑战是将已鉴定的肽段与其来源的蛋白质进行匹配,这一问题被称为蛋白质推断问题。冗余和同源蛋白质序列在正确鉴定方面存在挑战,因为在许多情况下,一组肽段可能代表多种蛋白质。解决这个问题的一个简单方法是分配能够解释已鉴定肽段的最少蛋白质数量。然而,使用这种极简主义方法是否能准确代表自然系统尚不确定。在本文中,我们利用最近引入的肽段可检测性概念对蛋白质推断问题进行了重新表述。我们还提出了一种启发式算法来解决这个问题,并在合成和真实蛋白质组学数据上评估了其性能。与最小蛋白质集算法的贪心实现相比,我们纳入肽段可检测性的解决方案表现更优。

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