Abstract

Emiliania huxleyi is a cosmopolitan coccolithophore that plays an essential role in global carbon and sulfur cycling, and contributes to marine cloud formation and climate regulation. Previously, the proteomic profile of Emiliania huxleyi was investigated using a three-dimensional separation strategy combined with liquid chromatography-tandem mass spectrometry (LC-MS/MS). The current study reuses the MS/MS spectra obtained, for the global discovery of post-translational modifications (PTMs) in this species without specific enrichment methods. Twenty-five different PTM types were examined using Trans-Proteomic Pipeline (Comet and PeptideProphet). Overall, 13,483 PTMs were identified in 7421 proteins. Methylation was the most frequent PTM with more than 2800 modified sites, and lysine was the most frequently modified amino acid with more than 4000 PTMs. The number of proteins identified increased by 22.5% to 18,780 after performing the PTM search. Compared to intact peptides, the intensities of some modified peptides were superior or equivalent. The intensities of some proteins increased dramatically after the PTM search. Gene ontology analysis revealed that protein persulfidation was related to photosynthesis in Emiliania huxleyi. Additionally, various membrane proteins were found to be phosphorylated. Thus, our global PTM discovery platform provides an overview of PTMs in the species and prompts further studies to uncover their biological functions. The combination of a three-dimensional separation method with global PTM search is a promising approach for the identification and discovery of PTMs in other species.

Highlights

  • Post-translational modifications (PTMs) of proteins are proteolytic cleavages or covalent addition of modifying groups to amino acids after protein biosynthesis

  • Bottom-up proteomics approaches have been used for PTM discovery using liquid chromatography-tandem mass spectrometry (LC-MS/MS) [3]

  • Identification of PTMs in this study was based on a bottom-up proteomic approach, which included protein extraction, enzymatic digestion, fractionation, and LC-MS/MS analysis

Read more

Summary

Introduction

Post-translational modifications (PTMs) of proteins are proteolytic cleavages or covalent addition of modifying groups to amino acids after protein biosynthesis. They play essential roles in regulating protein function, stability, complex formation, localization, and protein-protein interactions [1,2]. Different PTMs can be identified in the TPP by altering the search parameters (variable modifications) [9]. Sample fractionation can be carried out to reduce the sample complexity and increase the number of peptides and PTMs identified [16]. Sample fractionation for global PTM identification in Synechococcus was previously reported using two-dimensional LC, which revealed nearly 12,000 sites of 23 different PTMs in 6704 unique peptides and 2230 proteins [6]

Methods
Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call