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- W2190137329 abstract "SRM (selected reaction monitoring), a tandem mass spectrometry-based method characterized by high repeatability and accuracy, is an effective tool for the quantification of predetermined proteins. In this study, we built a time-scheduled dimethyl-SRM method that can provide the precise relative quantification of 92 proteins in one run. By applying this method to the Salmonella PhoP/PhoQ two-component system, we found that the expression of selected PhoP/PhoQ-activated proteins in response to Mg(2+) concentrations could be divided into two distinct patterns. For the time-course SRM experiment, we found that the dynamics of the selected PhoP/PhoQ-activated proteins could be divided into three distinct patterns, providing a new clue regarding PhoP/PhoQ activation and regulation. Moreover, the results for iron homeostasis proteins in response to Mg(2+) concentrations revealed that the PhoP/PhoQ two-component system may serve as a repressor for iron uptake proteins. And ribosomal protein levels clearly showed a response to different Mg(2+) concentrations and to time." @default.
- W2190137329 created "2016-06-24" @default.
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- W2190137329 date "2016-01-01" @default.
- W2190137329 modified "2023-09-27" @default.
- W2190137329 title "Analysis of Salmonella PhoP/PhoQ regulation by dimethyl-SRM-based quantitative proteomics" @default.
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- W2190137329 doi "https://doi.org/10.1016/j.bbapap.2015.10.003" @default.
- W2190137329 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26472331" @default.
- W2190137329 hasPublicationYear "2016" @default.
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