4.8 Article

Cotton Ti-IMAC: Developing Phosphorylated Cotton as a Novel Platform for Phosphopeptide Enrichment

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 15, Issue 41, Pages 47893-47901

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.3c08697

Keywords

Phosphoproteomics; Enrichment; Immobilizedmetal affinity chromatography; Cotton fiber; LC-MS/MS; Protein PTM analysis

Ask authors/readers for more resources

Protein phosphorylation is an important PTM involved in many cellular functions. This study developed a novel platform for phosphopeptide enrichment using a phosphorylated cotton-fiber-based Ti(IV)-IMAC material. The material showed high efficiency and selectivity in enriching phosphopeptides and demonstrated excellent sensitivity and specificity in complex biological samples.
Protein phosphorylation is an important post-translational modification (PTM), which is involved in many important cellular functions. Understanding protein phosphorylation at the molecular level is critical to deciphering its relevant biological processes and signaling networks. Mass spectrometry (MS) has become a powerful tool for the comprehensive profiling of protein phosphorylation. Yet the low ionization efficiency and low abundance of phosphopeptides among complex biological samples make its MS analysis challenging; an enrichment strategy with high efficiency and selectivity is always necessary prior to MS analysis. In this study, we developed a phosphorylated cotton-fiber-based Ti(IV)-IMAC material (termed as Cotton Ti-IMAC) that can serve as a novel platform for phosphopeptide enrichment. The cotton fiber can be effectively grafted with phosphate groups covalently in a single step, where the titanium ions can then be immobilized to enable capturing phosphopeptides. The material can be prepared using cost-effective reagents within only 4 h. Benefiting from the flexibility and filterability of cotton fibers, the material can be easily packed as a spin-tip and make the enrichment process convenient. Cotton Ti-IMAC successfully enriched phosphopeptides from protein standard digests and exhibited a high selectivity (BSA/beta-casein = 1000:1) and excellent sensitivity (0.1 fmol/mu L). Moreover, 2354 phosphopeptides were profiled in one LC-MS/MS injection after enriching from only 100 mu g of HeLa cell digests with an enrichment specificity of up to 97.51%. Taken together, we believe that Cotton Ti-IMAC can serve as a widely applicable and robust platform for achieving large-scale phosphopeptide enrichment and expanding our knowledge of phosphoproteomics in complex biological systems.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available