Bayesian Confidence Intervals for Multiplexed Proteomics Integrate Ion-statistics with Peptide Quantification Concordance.

TitleBayesian Confidence Intervals for Multiplexed Proteomics Integrate Ion-statistics with Peptide Quantification Concordance.
Publication TypeJournal Article
Year of Publication2019
AuthorsPeshkin, L, Gupta, M, Ryazanova, L, Wühr, M
JournalMol Cell Proteomics
Volume18
Issue10
Pagination2108-2120
Date Published2019 10
ISSN1535-9484
KeywordsBayes Theorem, HeLa Cells, Humans, Peptides, Proteomics, Tandem Mass Spectrometry
Abstract

<p>Multiplexed proteomics has emerged as a powerful tool to measure relative protein expression levels across multiple conditions. The relative protein abundances are inferred by comparing the signals generated by isobaric tags, which encode the samples' origins. Intuitively, the trust associated with a protein measurement depends on the similarity of ratios from the protein's peptides and the signal-strength of these measurements. However, typically the average peptide ratio is reported as the estimate of relative protein abundance, which is only the most likely ratio with a very naive model. Moreover, there is no sense on the confidence in these measurements. Here, we present a mathematically rigorous approach that integrates peptide signal strengths and peptide-measurement agreement into an estimation of the true protein ratio and the associated confidence (BACIQ). The main advantages of BACIQ are: (1) It removes the need to threshold reported peptide signal based on an arbitrary cut-off, thereby reporting more measurements from a given experiment; (2) Confidence can be assigned without replicates; (3) For repeated experiments BACIQ provides confidence intervals for the union, not the intersection, of quantified proteins; (4) For repeated experiments, BACIQ confidence intervals are more predictive than confidence intervals based on protein measurement agreement. To demonstrate the power of BACIQ we reanalyzed previously published data on subcellular protein movement on treatment with an Exportin-1 inhibiting drug. We detect ∼2× more highly significant movers, down to subcellular localization changes of ∼1%. Thus, our method drastically increases the value obtainable from quantitative proteomics experiments, helping researchers to interpret their data and prioritize resources. To make our approach easily accessible we distribute it via a Python/Stan package.</p>

DOI10.1074/mcp.TIR119.001317
Alternate JournalMol. Cell Proteomics
PubMed ID31311848
PubMed Central IDPMC6773559
Grant ListR01 HD073104 / HD / NICHD NIH HHS / United States
R01 HD091846 / HD / NICHD NIH HHS / United States
R35 GM128813 / GM / NIGMS NIH HHS / United States