Literature DB >> 28176526

MALDI versus ESI: The Impact of the Ion Source on Peptide Identification.

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


  13 in total

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Journal:  Mol Cell Proteomics       Date:  2020-08-12       Impact factor: 5.911

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Journal:  Methods Enzymol       Date:  2018-12-22       Impact factor: 1.600

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9.  MALDI-MS Analysis of Peptide Libraries Expands the Scope of Substrates for Farnesyltransferase.

Authors:  Garrett L Schey; Peter H Buttery; Emily R Hildebrandt; Sadie X Novak; Walter K Schmidt; James L Hougland; Mark D Distefano
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Review 10.  Modern Approaches in the Identification and Quantification of Immunogenic Peptides in Cereals by LC-MS/MS.

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