| Literature DB >> 28176526 |
Wiebke Maria Nadler1, Dietmar Waidelich2, Alexander Kerner1, Sabrina Hanke1, Regina Berg3, Andreas Trumpp1, Christoph Rösli1.
Abstract
For mass spectrometry-based proteomic analyses, electrospray ionization (ESI) and matrix-assisted laser desorption/ionization (MALDI) are the commonly used ionization techniques. To investigate the influence of the ion source on peptide detection in large-scale proteomics, an optimized GeLC/MS workflow was developed and applied either with ESI/MS or with MALDI/MS for the proteomic analysis of different human cell lines of pancreatic origin. Statistical analysis of the resulting data set with more than 72 000 peptides emphasized the complementary character of the two methods, as the percentage of peptides identified with both approaches was as low as 39%. Significant differences between the resulting peptide sets were observed with respect to amino acid composition, charge-related parameters, hydrophobicity, and modifications of the detected peptides and could be linked to factors governing the respective ion yields in ESI and MALDI.Entities:
Keywords: ESI; MALDI; ionization; peptide modification; proteomics
Mesh:
Substances:
Year: 2017 PMID: 28176526 DOI: 10.1021/acs.jproteome.6b00805
Source DB: PubMed Journal: J Proteome Res ISSN: 1535-3893 Impact factor: 4.466