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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.

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Journal ArticleDOI

Liquid chromatography with tandem mass spectrometry-based proteomic discovery in aging and Alzheimer’s disease

TL;DR: The methods and examples of liquid chromatography—electrospray ionization—tandem mass spectrometry— based proteomics, with and without quantification using isotope-coded affinity tags, in the investigation of aging and Alzheimer’s disease are presented.
Journal ArticleDOI

IsoQuant: A software tool for stable isotope labeling by amino acids in cell culture-based mass spectrometry quantitation

TL;DR: A new SILAC-based proteomics quantitation software tool, named IsoQuant, is reported, which is used to process high mass accuracy mass spectrometry data and offers a convenient quantitation framework to calculate peptide/protein relative abundance ratios.
Journal ArticleDOI

Urinary protein profiling by liquid chromatography/tandem mass spectrometry: ADAM28 is overexpressed in bladder transitional cell carcinoma

TL;DR: Three proteins, SPINK5, ADAM28 and PTP1, were also confirmed by Western blotting and showed significant differential expression compared with the control group and may be used as a possible biomarker of bladder cancer.
Journal ArticleDOI

Peptide correlation: A means to identify high quality quantitative information in large‐scale proteomic studies

TL;DR: This study shows that peptides that accurately reflect relative protein abundances in large-scale sample sets can be selected based on the correlation to each other, and provides an intuitive and simple procedure to obtain a high quality quantitative information from proteomics data.
References
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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.
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