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

被引:30
作者
Hasan, Nazim [1 ]
Wu, Hui-Fen [1 ,2 ,3 ]
Li, Yi-Hsien [1 ]
Nawaz, Mohd [1 ]
机构
[1] Natl Sun Yat Sen Univ, Dept Chem, Kaohsiung 80424, Taiwan
[2] Natl Sun Yat Sen Univ, Ctr Nanosci & Nanotechnol, Kaohsiung 80424, Taiwan
[3] Natl Sun Yat Sen Univ, Doctoral Degree Program Marine Biotechnol, Kaohsiung 80424, Taiwan
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; TIME-OF-FLIGHT; DESORPTION/IONIZATION ION-TRAP; MASS-SPECTROMETRY; PROTEIN DIGESTION; PHOSPHOPEPTIDE ENRICHMENT; PHOSPHORYLATED PEPTIDES; ENZYMATIC DIGESTION; TITANIUM-DIOXIDE; RAPID ANALYSIS; EFFICIENT PROTEOLYSIS;
D O I
10.1007/s00216-010-3573-3
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:2909 / 2919
页数:11
相关论文
共 55 条
[1]   Mass spectrometry in proteomics [J].
Aebersold, R ;
Goodlett, DR .
CHEMICAL REVIEWS, 2001, 101 (02) :269-295
[2]   Bare silica nanoparticles as concentrating and affinity probes for rapid analysis of aminothiols, lysozyme and peptide mixtures using atmospheric-pressure matrix-assisted laser desorption/ionization ion trap and matrix-assisted laser desorption/ionization time-of-flight mass spectrometry [J].
Agrawal, Kavita ;
Wu, Hui-Fen .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2008, 22 (03) :283-290
[3]   Efficient protein digestion with peptide separation in a micro-device interfaced to electrospray mass spectrometry [J].
Al-Lawati, H ;
Watts, P ;
Welham, KJ .
ANALYST, 2006, 131 (05) :656-663
[4]   In situ enrichment of phosphopeptides on MALDI plates functionalized by reactive landing of zirconium(IV)-n-propoxide ions [J].
Blacken, Grady R. ;
Volny, Michael ;
Vaisar, Tomas ;
Sadilek, Martin ;
Turecek, Frantisek .
ANALYTICAL CHEMISTRY, 2007, 79 (14) :5449-5456
[5]   Optimizing TiO2-based phosphopeptide enrichment for automated multidimensional liquid chromatography coupled to tandem mass spectrometry [J].
Cantin, Greg T. ;
Shock, Teresa R. ;
Park, Sung Kyu ;
Madhani, Hiten D. ;
Yates, John R., III .
ANALYTICAL CHEMISTRY, 2007, 79 (12) :4666-4673
[6]   Selective extraction and enrichment of multiphosphorylated peptides using polyarginine-coated diamond nanoparticles [J].
Chang, Chia-Kai ;
Wu, Chih-Che ;
Wang, Yi-Sheng ;
Chang, Huan-Cheng .
ANALYTICAL CHEMISTRY, 2008, 80 (10) :3791-3797
[7]   Rapid enrichment of phosphopeptides and phosphoproteins from complex samples using magnetic particles coated with alumina as the concentrating probes for MALDI MS analysis [J].
Chen, Cheng-Tai ;
Chen, Wei-Yu ;
Tsai, Pei-Jane ;
Chien, Kun-Yi ;
Yu, Jau-Song ;
Chen, Yu-Chie .
JOURNAL OF PROTEOME RESEARCH, 2007, 6 (01) :316-325
[8]   Fe3O4/TiO2 core/shell nanoparticles as affinity probes for the analysis of phosphopeptides using TiO2 surface-assisted laser desorption/ionization mass spectrometry [J].
Chen, CT ;
Chen, YC .
ANALYTICAL CHEMISTRY, 2005, 77 (18) :5912-5919
[9]   Acceleration of microwave-assisted enzymatic digestion reactions by magnetite beads [J].
Chen, Wei-Yu ;
Chen, Yu-Chie .
ANALYTICAL CHEMISTRY, 2007, 79 (06) :2394-2401
[10]   Protein concentration and enzyme digestion on microbeads for MALDI-TOF peptide mass mapping of proteins from dilute solutions [J].
Doucette, A ;
Craft, D ;
Li, L .
ANALYTICAL CHEMISTRY, 2000, 72 (14) :3355-3362