We present a computational pipeline for the quantification of peptides and proteins in label-free LC-MS/MS data sets. The pipeline is composed of tools from the OpenMS software framework and is applicable to the processing of large experiments (50+ samples). We describe several enhancements that we have introduced to OpenMS to realize the implementation of this pipeline. They include new algorithms for centroiding of raw data, for feature detection, for the alignment of multiple related measurements, and a new tool for the calculation of peptide and protein abundances. Where possible, we compare the performance of the new algorithms to that of their established counterparts in OpenMS. We validate the pipeline on the basis of two small data sets that provide ground truths for the quantification. There, we also compare our results to those of MaxQuant and Progenesis LC-MS, two popular alternatives for the analysis of label-free data. We then show how our software can be applied to a large heterogeneous data set of 58 LC-MS/MS runs.

BackgroundModern data generation techniques used in distributed systems biology research projects often create datasets of enormous size and diversity. We argue that in order to overcome the challenge of managing those large quantitative datasets and maximise the biological information extracted from them, a sound information system is required. Ease of integration with data analysis pipelines and other computational tools is a key requirement for it.ResultsWe have developed openBIS, an open source software framework for constructing user-friendly, scalable and powerful information systems for data and metadata acquired in biological experiments. openBIS enables users to collect, integrate, share, publish data and to connect to data processing pipelines. This framework can be extended and has been customized for different data types acquired by a range of technologies.ConclusionsopenBIS is currently being used by several SystemsX.ch and EU projects applying mass spectrometric measurements of metabolites and proteins, High Content Screening, or Next Generation Sequencing technologies. The attributes that make it interesting to a large research community involved in systems biology projects include versatility, simplicity in deployment, scalability to very large data, flexibility to handle any biological data type and extensibility to the needs of any research domain.

Summary Development of workflow and data management systems are challenging because of the need to provide a service for users with varying degrees of expertise from novices to experts with more knowledge than the developers. We have received feedback from users and developers on the functionality and usability of the Swiss Grid Proteomics Portal, now called iPortal, during its first year of operation. Monitoring and interaction with the production system under heavy use have provided further information on how to improve efficiency and stability. In a second, highly upgraded version of iPortal, we have introduced several new concepts based on this feedback. In this paper, we detail the requirements and the improvements we have made, and also give an outlook on future directions. Copyright © 2014 John Wiley & Sons, Ltd.

Background:The human pathogen Streptococcus pyogenes adapts to vascular leakage at the site of infection. Results: S. pyogenes modifies the production of 213 in plasma determined using quantitative proteomics. Conclusion:The results clarify the function of HSA-binding proteins in S. pyogenes. Significance: Our data demonstrates the power of the quantitative mass spectrometry strategy to investigate bacterial adaptation to a given environment.