4.5 Article

A Priori Intrinsic PTM Size Parameters for Predicting the Ion Mobilities of Modified Peptides

期刊

出版社

SPRINGER
DOI: 10.1007/s13361-016-1553-3

关键词

Ion mobility spectrometry; Peptides; Proteomics; Post-translational modifications

资金

  1. NIH K-INBRE [P20 GM103418]
  2. NSF First [EPS-0903806]
  3. NSF CAREER [CHE-1552640]
  4. Division Of Chemistry
  5. Direct For Mathematical & Physical Scien [1552640] Funding Source: National Science Foundation
  6. Office Of The Director
  7. Office of Integrative Activities [0903806] Funding Source: National Science Foundation

向作者/读者索取更多资源

The rising profile of ion mobility spectrometry (IMS) in proteomics has driven the efforts to predict peptide cross-sections. In the simplest approach, these are derived by adding the contributions of all amino acid residues and post-translational modifications (PTMs) defined by their intrinsic size parameters (ISPs). We show that the ISPs for PTMs can be calculated from properties of constituent atoms, and introduce the impact scores that govern the shift of cross-sections from the central mass-dependent trend for unmodified peptides. The ISPs and scores tabulated for 100 more common PTMs enable predicting the domains for modified peptides in the IMS/MS space that would guide subproteome investigations.

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