Your browser doesn't support javascript.
loading
Putting Humpty Dumpty Back Together Again: What Does Protein Quantification Mean in Bottom-Up Proteomics?
Plubell, Deanna L; Käll, Lukas; Webb-Robertson, Bobbie-Jo; Bramer, Lisa M; Ives, Ashley; Kelleher, Neil L; Smith, Lloyd M; Montine, Thomas J; Wu, Christine C; MacCoss, Michael J.
Afiliación
  • Plubell DL; Department of Genome Sciences, University of Washington, Seattle, Washington 98195 United States.
  • Käll L; Science for Life Laboratory, KTH - Royal Institute of Technology, Box 1031, 17121 Solna, Sweden.
  • Webb-Robertson BJ; Pacific Northwest National Laboratory, Richland, Washington 99352, United States.
  • Bramer LM; Pacific Northwest National Laboratory, Richland, Washington 99352, United States.
  • Ives A; Proteomics Center of Excellence & Departments of Chemistry and Molecular Biosciences, Northwestern University, Evanston, Illinois 60208, United States.
  • Kelleher NL; Proteomics Center of Excellence & Departments of Chemistry and Molecular Biosciences, Northwestern University, Evanston, Illinois 60208, United States.
  • Smith LM; Department of Chemistry, University of Wisconsin-Madison, Madison, Wisconsin 53706, United States.
  • Montine TJ; Department of Pathology, Stanford University, Stanford, California 94305, United States.
  • Wu CC; Department of Genome Sciences, University of Washington, Seattle, Washington 98195 United States.
  • MacCoss MJ; Department of Genome Sciences, University of Washington, Seattle, Washington 98195 United States.
J Proteome Res ; 21(4): 891-898, 2022 04 01.
Article en En | MEDLINE | ID: mdl-35220718
Bottom-up proteomics provides peptide measurements and has been invaluable for moving proteomics into large-scale analyses. Commonly, a single quantitative value is reported for each protein-coding gene by aggregating peptide quantities into protein groups following protein inference or parsimony. However, given the complexity of both RNA splicing and post-translational protein modification, it is overly simplistic to assume that all peptides that map to a singular protein-coding gene will demonstrate the same quantitative response. By assuming that all peptides from a protein-coding sequence are representative of the same protein, we may miss the discovery of important biological differences. To capture the contributions of existing proteoforms, we need to reconsider the practice of aggregating protein values to a single quantity per protein-coding gene.
Asunto(s)
Palabras clave

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Proteómica Idioma: En Revista: J Proteome Res Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Proteínas / Proteómica Idioma: En Revista: J Proteome Res Asunto de la revista: BIOQUIMICA Año: 2022 Tipo del documento: Article