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Comparison of higher energy collisional dissociation and collision‐induced dissociation MS/MS sequencing methods for identification of naturally occurring peptides in human urine
Author(s) -
Pejchinovski Martin,
Klein Julie,
RamírezTorres Adela,
Bitsika Vasiliki,
Mermelekas George,
Vlahou Antonia,
Mullen William,
Mischak Harald,
Jankowski Vera
Publication year - 2015
Publication title -
proteomics – clinical applications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.948
H-Index - 54
eISSN - 1862-8354
pISSN - 1862-8346
DOI - 10.1002/prca.201400163
Subject(s) - chemistry , peptide , reproducibility , chromatography , dissociation (chemistry) , fragmentation (computing) , urine , analytical chemistry (journal) , biochemistry , biology , organic chemistry , ecology
Purpose The aim of this study is to determine the best fragmentation method for sequence identification of naturally occurring urinary peptides in the field of clinical proteomics. Experimental design We used LC‐MS/MS analysis of urine samples to determine the analytical performance of higher energy collisional dissociation (HCD), CID with high and low resolution MS/MS for the identification of naturally occurring peptides in the low molecular weight urinary proteome. Results HCD and CID high‐resolution generated a 22% error rate in peptide sequence identifications. CID low‐resolution showed significantly higher error rates (37%). Excluding the error rate (i.e rejection of cysteine‐containing peptides), we observed a higher degree of overlap between HCD and CID high resolution for identification of peptide sequences of rank 1 and cross‐correlation ≥ 1.9 (262 peptide sequences) compared to CID low (208 peptide sequences with HCD and 192 peptide sequences with CID high). Reproducibility of detected peptides in three out of the five replicates was also higher in HCD and CID high in relation to CID low resolution. Conclusion and clinical relevance Our data demonstrated that HCD and CID high‐resolution performed with better accuracy and reproducibility than CID low resolution in respect to the identification of naturally occurring urinary peptide sequences.