Monitoring of Plant Protein Post-translational Modifications Using Targeted Proteomics

被引:35
作者
Arsova, Borjana [1 ]
Watt, Michelle [1 ]
Usadel, Bjoern [1 ,2 ]
机构
[1] Forschungszentrum Julich, Inst Bio & Geowissensch, IBG Plant Sci 2, Julich, Germany
[2] Rhein Westfal TH Aachen, IBMG Inst Biol 1, Aachen, Germany
来源
FRONTIERS IN PLANT SCIENCE | 2018年 / 9卷
关键词
targeted proteomics; plants; Arabidopsis; Berley; SRM/MRM; post translational modification; phosphorylation; ubiquitination; PHOSPHORYLATION SITE DATABASE; ORBITRAP MASS-SPECTROMETER; PLASMA-MEMBRANE PROTEINS; ARABIDOPSIS-THALIANA; PHOSPHOENOLPYRUVATE CARBOXYLASE; QUANTITATIVE PHOSPHOPROTEOMICS; ABSOLUTE QUANTITATION; KINASE; NITRATE; IDENTIFICATION;
D O I
10.3389/fpls.2018.01168
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Protein post-translational modifications (PTMs) are among the fastest and earliest of plant responses to changes in the environment, making the mechanisms and dynamics of PTMs an important area of plant science. One of the most studied PTMs is protein phosphorylation. This review summarizes the use of targeted proteomics for the elucidation of the biological functioning of plant PTMs, and focuses primarily on phosphorylation. Since phosphorylated peptides have a low abundance, usually complex enrichment protocols are required for their research. Initial identification is usually performed with discovery phosphoproteomics, using high sensitivity mass spectrometers, where as many phosphopeptides are measured as possible. Once a PTM site is identified, biological characterization can be addressed with targeted proteomics. In targeted proteomics, Selected/Multiple Reaction Monitoring (S/MRM) is traditionally coupled to simple, standard protein digestion protocols, often omitting the enrichment step, and relying on triple-quadruplemass spectrometer. The use of synthetic peptides as internal standards allows accurate identification, avoiding cross-reactivity typical for some antibody based approaches. Importantly, internal standards allow absolute peptide quantitation, reported down to 0.1 femtomoles, also useful for determination of phospho-site occupancy. S/MRM is advantageous in situations where monitoring and diagnostics of peptide PTM status is needed for many samples, as it has faster sample processing times, higher throughput than other approaches, and excellent quantitation and reproducibility. Furthermore, the number of publicly available data-bases with plant PTM discovery data is growing, facilitating selection of modified peptides and design of targeted proteomics workflows. Recent instrument developments result in faster scanning times, inclusion of ion-trap instruments leading to parallel reaction monitoring-which further facilitates S/MRM experimental design. Finally, recent combination of data independent and data dependent spectra acquisition means that in addition to anticipated targeted data, spectra can now be queried for unanticipated information. The potential for future applications in plant biology is outlined.
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页数:9
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