scispace - formally typeset
Journal ArticleDOI

Automated statistical analysis of protein abundance ratios from data generated by stable-isotope dilution and tandem mass spectrometry.

TLDR
The utility of the ASAPRatio program was clearly demonstrated by its speed and the accuracy of the generated protein abundance ratios and by its capability to identify specific core components of the RNA polymerase II transcription complex within a high background of copurifying proteins.
Abstract
We describe an algorithm for the automated statistical analysis of protein abundance ratios (ASAPRatio) of proteins contained in two samples. Proteins are labeled with distinct stable-isotope tags and fragmented, and the tagged peptide fragments are separated by liquid chromatography (LC) and analyzed by electrospray ionization (ESI) tandem mass spectrometry (MS/MS). The algorithm utilizes the signals recorded for the different isotopic forms of peptides of identical sequence and numerical and statistical methods, such as Savitzky-Golay smoothing filters, statistics for weighted samples, and Dixon's test for outliers, to evaluate protein abundance ratios and their associated errors. The algorithm also provides a statistical assessment to distinguish proteins of significant abundance changes from a population of proteins of unchanged abundance. To evaluate its performance, two sets of LC-ESI-MS/MS data were analyzed by the ASAPRatio algorithm without human intervention, and the data were related to the expected and manually validated values. The utility of the ASAPRatio program was clearly demonstrated by its speed and the accuracy of the generated protein abundance ratios and by its capability to identify specific core components of the RNA polymerase II transcription complex within a high background of copurifying proteins.

read more

Content maybe subject to copyright    Report

Citations
More filters
Book ChapterDOI

Software Development for Quantitative Proteomics Using Stable Isotope Labeling

TL;DR: This chapter presents a quantification program, termed UNiquant, for analyzing quantitative proteomic data using SIL, and evaluated the pros and cons of the quantification results from two different MS acquisition modes, data-dependent acquisition and data-independent acquisition.
Journal ArticleDOI

Differential Human Plasma Proteomics Based on AniBal Quantification and Peptide-level Off-Gel Isoelectric Focussing:

TL;DR: The combined methods consisting of MARS, AniBAL, Off-Gel and nano-LC-MS/MS on a Bruker HCT ion trap represent a new and efficient platform to quantify human plasma proteome differences between conditions.
Journal ArticleDOI

Annotator: Postprocessing Software for Generating Function-based Signatures from Quantitative Mass Spectrometry

TL;DR: Annotator is an application that filters validated mass spectrometry data and applies a battery of standardized heuristic and statistical tests to determine significance, providing a consistent and quantitative method for formulating conclusions about cellular behavior, independent of network models or standard enrichment analyses.
Journal ArticleDOI

MetaMSD: meta analysis for mass spectrometry data.

TL;DR: This article introduces a meta-analysis software, MetaMSD (Meta Analysis for Mass Spectrometry Data), that is specifically designed for mass spectrometry data and will help proteomics researchers fully utilize the benefit of multiple studies (or datasets), thus optimizing biomarker discovery.
References
More filters
Journal ArticleDOI

Probability-based protein identification by searching sequence databases using mass spectrometry data.

TL;DR: A new computer program, Mascot, is presented, which integrates all three types of search for protein identification by searching a sequence database using mass spectrometry data, and the scoring algorithm is probability based.
Journal ArticleDOI

A statistical model for identifying proteins by tandem mass spectrometry.

TL;DR: A statistical model is presented for computing probabilities that proteins are present in a sample on the basis of peptides assigned to tandem mass (MS/MS) spectra acquired from a proteolytic digest of the sample, and it is shown to produce probabilities that are accurate and have high power to discriminate correct from incorrect protein identifications.
Journal ArticleDOI

Integrated genomic and proteomic analyses of a systematically perturbed metabolic network.

TL;DR: An integrated approach to build, test, and refine a model of a cellular pathway, in which perturbations to critical pathway components are analyzed using DNA microarrays, quantitative proteomics, and databases of known physical interactions, suggests hypotheses about the regulation of galactose utilization and physical interactions between this and a variety of other metabolic pathways.
Journal ArticleDOI

Linking genome and proteome by mass spectrometry: Large-scale identification of yeast proteins from two dimensional gels

TL;DR: This study establishes that mass spectrometry provides the required throughput, the certainty of identification, and the general applicability to serve as the method of choice to connect genome and proteome.
Journal ArticleDOI

A proteomics strategy to elucidate functional protein-protein interactions applied to EGF signaling

TL;DR: Stable isotopic amino acids in cell culture is employed to differentially label proteins in EGF-stimulated versus unstimulated cells and SILAC combined with modification-based affinity purification is a useful approach to detect specific and functional protein-protein interactions.
Related Papers (5)