Kenyani Jenna, Medina-Aunon J Alberto, Martinez-Bartolomé Salvador, Albar Juan-Pablo, Wastling Jonathan M, Jones Andrew R
Institute of Integrative Biology, University of Liverpool, Biosciences Building, Crown Street, Liverpool, UK.
BMC Res Notes. 2011 Mar 28;4:86. doi: 10.1186/1756-0500-4-86.
Proteomic techniques allow researchers to perform detailed analyses of cellular states and many studies are published each year, which highlight large numbers of proteins quantified in different samples. However, currently few data sets make it into public databases with sufficient metadata to allow other groups to verify findings, perform data mining or integrate different data sets. The Proteomics Standards Initiative has released a series of "Minimum Information About a Proteomics Experiment" guideline documents (MIAPE modules) and accompanying data exchange formats. This article focuses on proteomic studies based on gel electrophoresis and demonstrates how the corresponding MIAPE modules can be fulfilled and data deposited in public databases, using a new experimental data set as an example.
We have performed a study of the effects of an anabolic agent (salbutamol) at two different time points on the protein complement of rat skeletal muscle cells, quantified by difference gel electrophoresis. In the DIGE study, a total of 31 non-redundant proteins were identified as being potentially modulated at 24 h post treatment and 110 non redundant proteins at 96 h post-treatment. Several categories of function have been highlighted as strongly enriched, providing candidate proteins for further study. We also use the study as an example of best practice for data deposition.
We have deposited all data sets from this study in public databases for further analysis by the community. We also describe more generally how gel-based protein identification data sets can now be deposited in the PRoteomics IDEntifications database (PRIDE), using a new software tool, the PRIDESpotMapper, which we developed to work in conjunction with the PRIDE Converter application. We also demonstrate how the ProteoRed MIAPE generator tool can be used to create and share a complete and compliant set of MIAPE reports for this experiment and others.
蛋白质组学技术使研究人员能够对细胞状态进行详细分析,每年都有许多相关研究发表,这些研究突出了在不同样本中定量的大量蛋白质。然而,目前很少有数据集能够以足够的元数据进入公共数据库,以使其他研究团队能够验证研究结果、进行数据挖掘或整合不同的数据集。蛋白质组学标准倡议组织已经发布了一系列“蛋白质组学实验最小信息”指南文件(MIAPE模块)及相应的数据交换格式。本文重点关注基于凝胶电泳的蛋白质组学研究,并以一个新的实验数据集为例,展示如何完成相应的MIAPE模块并将数据存入公共数据库。
我们进行了一项研究,考察了一种合成代谢剂(沙丁胺醇)在两个不同时间点对大鼠骨骼肌细胞蛋白质组的影响,采用差异凝胶电泳进行定量分析。在该差异凝胶电泳研究中,共鉴定出31种非冗余蛋白在处理后24小时可能受到调控,110种非冗余蛋白在处理后96小时受到调控。已突出显示了几类功能显著富集,为进一步研究提供了候选蛋白。我们还将该研究作为数据存档最佳实践的示例。
我们已将本研究的所有数据集存入公共数据库,以供同行进一步分析。我们还更全面地描述了如何使用我们开发的与PRIDE Converter应用程序协同工作的新软件工具PRIDESpotMapper,将基于凝胶的蛋白质鉴定数据集存入蛋白质组学鉴定数据库(PRIDE)。我们还展示了如何使用ProteoRed MIAPE生成工具为该实验及其他实验创建并共享一套完整且合规的MIAPE报告。