Cranfield Health, Cranfield Bioinformatics Group, Cranfield University Bedfordshire, UK.
Front Plant Sci. 2012 Jul 20;3:164. doi: 10.3389/fpls.2012.00164. eCollection 2012.
Selected reaction monitoring (SRM), sometimes called multiple reaction monitoring (MRM), is becoming the tool of choice for targeted quantitative proteomics in the plant science community. Key to a successful SRM experiment is prior identification of the distinct peptides for the proteins of interest and the determination of the so-called transitions that can be programmed into an LC-MS/MS to monitor those peptides. The transition for a given peptide comprises the intact peptide m/z and a high intensity product ion that can be monitored at a characteristic retention time (RT). To aid the design of SRM experiments, several online tools and databases have been produced to help researchers select transitions for their proteins of interest, but many of these tools are limited to the most popular model organisms such as human, yeast, and mouse or require the experimental acquisition of local spectral libraries. In this paper we present MRMaid, a web-based SRM assay design tool whose transitions are generated by mining the millions of identified peptide spectra held in the EBI's PRIDE database. By using data from this large public repository, MRMaid is able to cover a wide range of species that can increase as the coverage of PRIDE grows. In this paper MRMaid transitions for 25 Arabidopsis thaliana proteins are evaluated experimentally, and found capable of quantifying 23 of these proteins. This performance was found to be comparable with the more time consuming approach of designing transitions using locally acquired orbitrap data, indicating that MRMaid is a valuable tool for targeted Arabidopsis proteomics.
选择反应监测(SRM),有时也称为多重反应监测(MRM),在植物科学领域已成为靶向定量蛋白质组学的首选工具。成功进行 SRM 实验的关键是事先确定感兴趣蛋白质的独特肽,并确定可以编程到 LC-MS/MS 中以监测这些肽的所谓转换。给定肽的转换包括完整肽 m/z 和可以在特征保留时间(RT)监测到的高强度产物离子。为了帮助设计 SRM 实验,已经开发了几种在线工具和数据库来帮助研究人员为他们感兴趣的蛋白质选择转换,但其中许多工具仅限于最受欢迎的模式生物,如人类、酵母和小鼠,或者需要实验获取本地光谱库。在本文中,我们介绍了 MRMaid,这是一种基于网络的 SRM 检测设计工具,其转换是通过挖掘 EBI 的 PRIDE 数据库中存储的数百万个已识别肽谱来生成的。通过使用来自这个大型公共存储库的数据,MRMaid 能够涵盖广泛的物种,随着 PRIDE 覆盖范围的扩大,物种数量还会增加。在本文中,我们实验评估了 25 种拟南芥蛋白质的 MRMaid 转换,发现能够定量 23 种蛋白质。与使用本地获取的轨道阱数据设计转换的更耗时方法相比,这种性能相当,表明 MRMaid 是靶向拟南芥蛋白质组学的有价值的工具。