出 处:《World Journal of Gastroenterology》2011年第5期618-624,共7页世界胃肠病学杂志(英文版)
基 金:Supported by The National Science and Technology Pillar Program of the Ministry of Science and Technology of the People’s Republic of China during the Eleventh Five-Year plan period,No. 2007BAID4B02
摘 要:AIM: To investigate the relationship between urinary peptide changes and Helicobacter pylori (H. pylorl) infection using urinary peptidome profiling. METHODS: The study was performed in volunteers (n = 137) who gave informed consent. Urinary peptides were enriched by magnetic beads based weak cation exchange chromatography'and spectrums acquired by matrix-assisted laser desorption/ionization time-of-flight (MALDI-TOF) mass spectrometry (MS). ClinProTools bioinformatics software was used for statistical analysis and the recognition of peptide patterns. The marker peptides were identified by LTQ Obitrap XL tandem MS. RESULTS: Approximately 50 proteins or peptides which loaded onto the magnetic beads were detected by MAL-DI-TOF MS. By optimizing the parameters of the model, the Genetic Algorithm model had good recognition capability (97%) and positive predictive value (94%). Based on the model, 2 markers with molecular masses of 6788 and 1912 Da were found that differentiated between H. pylori positive and negative volunteers. The m/z 1912 sequence was parsed as SKQFTSSTSYN- RGDSTF. The peptide was identified as isoform 1 of the fibrinogen a chain precursor, whose concentration in urine was markedly higher in H. pylori infected volunteers than in H. pylori non-infected ones. CONCLUSION: The appearance of urinary fibrinogen degradation products is caused by an active H. pyloriinduced process.AIM:To investigate the relationship between urinary peptide changes and Helicobacter pylori(H.pylori) infection using urinary peptidome profiling.METHODS:The study was performed in volunteers(n = 137) who gave informed consent.Urinary peptides were enriched by magnetic beads based weak cation exchange chromatography and spectrums acquired by matrix-assisted laser desorption/ionization time-of-flight(MALDI-TOF) mass spectrometry(MS).ClinProTools bioinformatics software was used for statistical analysis and the recognition of peptide patterns.The marker peptides were identified by LTQ Obitrap XL tandem MS.RESULTS:Approximately 50 proteins or peptides which loaded onto the magnetic beads were detected by MALDI-TOF MS.By optimizing the parameters of the model,the Genetic Algorithm model had good recognition capability(97%) and positive predictive value(94%).Based on the model,2 markers with molecular masses of 6788 and 1912 Da were found that differentiated between H.pylori positive and negative volunteers.The m/z 1912 sequence was parsed as SKQFTSSTSYNRGDSTF.The peptide was identified as isoform 1 of the fibrinogen α chain precursor,whose concentration in urine was markedly higher in H.pylori infected volunteers than in H.pylori non-infected ones.CONCLUSION:The appearance of urinary fibrinogen degradation products is caused by an active H.pyloriinduced process.
关 键 词:Urinary peptidome profiling MB-matrix-assisted laser desorption/ionization time-of-flight massspectrometry Helicobacter pylori Fibrinogen degrada-tion products
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