4.7 Article

Efficient Marginalization to Compute Protein Posterior Probabilities from Shotgun Mass Spectrometry Data

Journal

JOURNAL OF PROTEOME RESEARCH
Volume 9, Issue 10, Pages 5346-5357

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/pr100594k

Keywords

protein identification; tandem mass spectrometry; Bayesian methods; degenerate peptides

Funding

  1. NIH [R01 EB007057, P41 RR0011823]

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The problem of identifying proteins from a shotgun proteomics experiment has not been definitively solved. Identifying the proteins in a sample requires ranking them, ideally with interpretable scores. In particular, degenerate peptides, which map to multiple proteins, have made such a ranking difficult to compute. The problem of computing posterior probabilities for the proteins, which can be interpreted as confidence in a protein's presence, has been especially daunting. Previous approaches have either ignored the peptide degeneracy problem completely, addressed it by computing a heuristic set of proteins or heuristic posterior probabilities, or estimated the posterior probabilities with sampling methods. We present a probabilistic model for protein identification in tandem mass spectrometry that recognizes peptide degeneracy. We then introduce graph-transforming algorithms that facilitate efficient computation of protein probabilities, even for large data sets. We evaluate our identification procedure on five different well-characterized data sets and demonstrate our ability to efficiently compute high-quality protein posteriors.

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