4.7 Article

Two-step on-particle ionization/enrichment via a washing- and separation-free approach: multifunctional TiO2 nanoparticles as desalting, accelerating, and affinity probes for microwave-assisted tryptic digestion of phosphoproteins in ESI-MS and MALDI-MS: comparison with microscale TiO2

期刊

ANALYTICAL AND BIOANALYTICAL CHEMISTRY
卷 396, 期 8, 页码 2909-2919

出版社

SPRINGER HEIDELBERG
DOI: 10.1007/s00216-010-3573-3

关键词

Microwave-assisted tryptic digestion; TiO2 nanoparticles; Protein; Phosphopeptide enrichment; Electrospray ionization mass spectrometry; Matrix-assisted laser desorption ionization time of flight mass spectrometry

资金

  1. National Science Council of Taiwan

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We introduce a simplified sample preparation method using bare TiO2 nanoparticles (NPs) to serve as multifunctional nanoprobes (desalting, accelerating, and affinity probes) for effective enrichment of phosphopeptides from microwave-assisted tryptic digestion of phosphoproteins (alpha-casein, beta-casein and milk) in Electrospray Ionization Mass Spectrometry (ESI-MS) and Matrix Assisted Laser Desorption Ionization Mass Spectrometry (MALDI-MS). The results demonstrate that TiO2 NPs can effectively enrich and accelerate the digestion reactions of phosphoproteins in aqueous solutions and also from complex real samples. After the microwave experiments, we directly injected the resulting solutions into the ESI-MS and MALDI-MS systems for analysis, and excellent sensitivity was achieved without the need for any washing procedure or separation process. The reasons are attributed to the high binding affinity and selectivity of TiO2 NPs toward phosphopeptides. Thus, phosphopeptides can be adsorbed onto the TiO2 NP surface. The digested or partially digested phosphoproteins can be concentrated onto the TiO2 NP surface. This results in the effective or complete digestion of phosphoproteins in a short period of time (45 s). In addition, high sensitivity and sequence coverage of phosphopeptide can be obtained using TiO2 NPs as microwave absorbers and affinity probes in MALDI-MS and ESI-MS. This is due to the photocatalytic nature of the TiO2 NPs because the absorption of microwave radiation that can accelerate the activation of trypsin for efficient digestion of phosphoproteins and enhances the ionization of phosphopeptides. The lowest concentrations detected for ESI-MS and MALDI-MS were 0.1 mu M and 10 fmol, respectively, for alpha-casein. Comparing the two-step approach of TiO2 NPs with microscale TiO2 particles, the microscale TiO2 particles shows no effect on the microwave-assisted tryptic digestion of phosphoproteins. The current approach offers multiple advantages, such as great simplicity, high sensitivity and selectivity, straightforward and separation/washing-free technique for phosphorpeptide enrichment analysis.

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