ZrO₂ Nanofiber as a Versatile Tool for Protein Analysis

Abstract

Phosphorylation is one of the most important post-translational modifications in proteins. Their essential roles in the regulation of cellular processes and alteration of protein-protein interaction networks have been actively studied. However, phosphorylated proteins are present at low abundance in cells, and ionization of the modified peptides is often suppressed by the more abundant species in mass spectrometry. Effective enrichment techniques are needed to remove the unmodified peptides and concentrate the phosphorylated ones before their identification and quantification. Herein, we prepared ZrO2 nanofibers by electrospinning, a straightforward and easy fabrication technique, and applied them to enrich phosphorylated peptides and proteins. The fibers showed good size homogeneity and porosity and could specifically bind to the phosphorylated peptides and proteins, allowing their separation from the unmodified analogues when present in either simple protein digests or highly complex cell lysates. The enrichment performance was superior to that of the commercially available nanoparticles. Moreover, modifying the solution pH could lead to selective adsorption of proteins with different pI values, suggesting the fibers' potential applicability in charge-based protein fractionation. Our results support that the electrospun ZrO2 nanofibers can serve as a versatile tool for protein analysis with great ease in preparation and handling.

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“…[43][44][45] Correspondingly, the specic surface area of FZR, 72 m 2 g À1 , is in the higher end of literature values (5.9-106.3 m 2 g À1 ) for pure and doped zirconium oxide nanobers. 14,41,[46][47][48] Titration. Potentiometric titration was conducted to determine acidic nature of the zirconium oxide materials, Fig.…”

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Nanomaterials in Proteomics

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