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IsoBayes: a Bayesian approach for single-isoform proteomics inference.
Bollon, Jordy; Shortreed, Michael R; Jordan, Ben T; Miller, Rachel; Jeffery, Erin; Cavalli, Andrea; Smith, Lloyd M; Dewey, Colin; Sheynkman, Gloria M; Tiberi, Simone.
Afiliación
  • Bollon J; Computational and Chemical Biology, Italian Institute of Technology, CMPVdA, Aosta, Italy.
  • Shortreed MR; Astronomical Observatory of the Autonomous Region of the Aosta Valley (OAVdA), Nus, Italy.
  • Jordan BT; Department of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
  • Miller R; Frederick National Laboratory for Cancer Research, Frederick, MD, USA.
  • Jeffery E; Department of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
  • Cavalli A; Department of Molecular Physiology and Biological Physics, University of Virginia, Charlottesville, VA, USA.
  • Smith LM; Computational and Chemical Biology, Italian Institute of Technology, CMPVdA, Aosta, Italy.
  • Dewey C; Centre Européen de Calcul Atomique et Moléculaire, École Polytechnique Fédérale de Lausanne, Lausanne, Switzerland.
  • Sheynkman GM; Department of Chemistry, University of Wisconsin-Madison, Madison, WI, USA.
  • Tiberi S; Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, WI, USA.
bioRxiv ; 2024 Jun 11.
Article en En | MEDLINE | ID: mdl-38915658
ABSTRACT
Studying protein isoforms is an essential step in biomedical research; at present, the main approach for analyzing proteins is via bottom-up mass spectrometry proteomics, which return peptide identifications, that are indirectly used to infer the presence of protein isoforms. However, the detection and quantification processes are noisy; in particular, peptides may be erroneously detected, and most peptides, known as shared peptides, are associated to multiple protein isoforms. As a consequence, studying individual protein isoforms is challenging, and inferred protein results are often abstracted to the gene-level or to groups of protein isoforms. Here, we introduce IsoBayes, a novel statistical method to perform inference at the isoform level. Our method enhances the information available, by integrating mass spectrometry proteomics and transcriptomics data in a Bayesian probabilistic framework. To account for the uncertainty in the measurement process, we propose a two-layer latent variable

approach:

first, we sample if a peptide has been correctly detected (or, alternatively filter peptides); second, we allocate the abundance of such selected peptides across the protein(s) they are compatible with. This enables us, starting from peptide-level data, to recover protein-level data; in particular, we i) infer the presence/absence of each protein isoform (via a posterior probability), ii) estimate its abundance (and credible interval), and iii) target isoforms where transcript and protein relative abundances significantly differ. We benchmarked our approach in simulations, and in two multi-protease real datasets our method displays good sensitivity and specificity when detecting protein isoforms, its estimated abundances highly correlate with the ground truth, and can detect changes between protein and transcript relative abundances. IsoBayes is freely distributed as a Bioconductor R package, and is accompanied by an example usage vignette.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Italia

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: BioRxiv Año: 2024 Tipo del documento: Article País de afiliación: Italia