| Literature DB >> 26457653 |
Jürgen Claesen1, Frederik Lermyte, Frank Sobott, Tomasz Burzykowski1, Dirk Valkenborg1,2.
Abstract
The elemental isotope definition used to calculate the theoretical masses and isotope distribution of (bio)molecules is considered to be a fixed, universal standard in mass-spectrometry-based proteomics. However, this is an incorrect assumption. In view of the ongoing advances in mass spectrometry technology, and in particular the ever-increasing mass precision, the elemental isotope definition and its variations should be taken into account. We illustrate the effect of the elemental isotope uncertainty on the theoretical and experimental masses with theoretical calculations and examples.Mesh:
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Year: 2015 PMID: 26457653 DOI: 10.1021/acs.analchem.5b01165
Source DB: PubMed Journal: Anal Chem ISSN: 0003-2700 Impact factor: 6.986