| Literature DB >> 29812944 |
Lazaro Hiram Betancourt1, Aniel Sanchez1, Indira Pla1, Magdalena Kuras1, Qimin Zhou2, Roland Andersson2, Gyorgy Marko-Varga1,3.
Abstract
Urea-containing buffer solutions are generally used in proteomic studies to aid protein denaturation and solubilization during cell and tissue lysis. It is well-known, however, that urea can lead to carbamylation of peptides and proteins and, subsequently, incomplete digestion of proteins. By the use of cells and tissues that had been lysed with urea, different solution digestion strategies were quantitatively assessed. In comparison with traditional proteolysis at 37 °C, urea in-solution digestion performed at room temperature improved peptide and protein identification and quantitation and had a minimum impact on miscleavage rates. Furthermore, the signal intensities and the number of carbamylated and pyroglutamic acid-modified peptides decreased. Overall, this led to a reduction in the negative effects often observed for such modifications. Data are available via ProteomeXchange with identifier PXD009426.Entities:
Keywords: carbamylation; in-solution digestion; label-free quantification; mass spectrometry; proteomics; temperature; urea
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Year: 2018 PMID: 29812944 DOI: 10.1021/acs.jproteome.8b00228
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466