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Re-mining serum proteomics data reveals extensive post-translational modifications upon Zika and dengue infection

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MOLECULAR OMICS
卷 19, 期 4, 页码 308-320

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2mo00258b

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Due to the implications for pregnancy outcomes, understanding the molecular differences between Zika virus (ZIKV) and dengue virus (DENV) infections is of high interest. Through analyzing mass spectra, researchers identified 246 modified peptides with significantly differential abundance in ZIKV and DENV patients. Methionine-oxidized peptides from apolipoproteins and glycosylated peptides from immunoglobulin proteins were found to be more abundant in ZIKV patients, providing insights into the potential roles of these modifications in the infection.
Zika virus (ZIKV) and dengue virus (DENV) are two closely related flaviviruses with similar symptoms. However, due to the implications of ZIKV infections for pregnancy outcomes, understanding differences in their molecular impact on the host is of high interest. Viral infections change the host proteome, including post-translational modifications. As modifications are diverse and of low abundance, they typically require additional sample processing which is not feasible for large cohort studies. Therefore, we tested the potential of next-generation proteomics data in its ability to prioritize specific modifications for later analysis. We re-mined published mass spectra from 122 serum samples from ZIKV and DENV patients for the presence of phosphorylated, methylated, oxidized, glycosylated/glycated, sulfated, and carboxylated peptides. We identified 246 modified peptides with significantly differential abundance in ZIKV and DENV patients. Amongst these, methionine-oxidized peptides from apolipoproteins and glycosylated peptides from immunoglobulin proteins were more abundant in ZIKV patient serum and generate hypotheses on the potential roles of the modification in the infection. The results demonstrate how data-independent acquisition techniques can help prioritize future analyses of peptide modifications.

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