4.4 Article

Effect of urea surface modification and photocatalytic cleaning on surface-assisted laser desorption ionization mass spectrometry with amorphous TiO2 nanoparticles

Journal

JOURNAL OF MASS SPECTROMETRY
Volume 44, Issue 10, Pages 1443-1451

Publisher

WILEY
DOI: 10.1002/jms.1628

Keywords

SALDI-MS; TiO2 nanoparticles; urea-surface modification; photocatalytic cleaning; phosphopeptides; pyrene

Funding

  1. Japan Society for the Promotion of Science [20710091, 19350045]
  2. Ministry of Education, Culture, Sports, Science, and Technology-Japan (MEXT) [18004]
  3. Grants-in-Aid for Scientific Research [19350045, 20710091] Funding Source: KAKEN

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We have investigated the effect of urea surface modification and the photocatalytic cleaning on surface-assisted laser desorption ionization mass spectrometry (SALDI-MS) with amorphous TiO2 nanoparticles for the reduction of the background noise and the improvement of the sensitivity. In the use of nanoparticles of high surface area, chemical background signals arising from ambient environments and organic contaminants can frequently be serious problems below 500 Da, possibly reducing the advantages of the matrix-free approach. In this study, removal of contaminants and enhanced SALDI efficiency were easily achieved with UV irradiation via the photocatalyst effect of TiO2 before SALDI-MS measurements. The surface cleaning achieved by the UV photocatalytic procedure reduced the background noise and increased the peak intensities of peptides. in addition, we found that urea surface modification of TiO2 nanoparticles increased the performance of the TiO2-SALDI-MS. (1) The urea-surface modification of TiO2 made it possible to produce proton-adduct forms without citrate buffer, resulting in low background noises below 500 Da, in contrast to the essential use of a citrate buffer in the bare TiO2-SALDI-MS. (2) The detection sensitivity of angiotensin I increased to 0.3 fmol with the urea-surface modification, as compared to the use of bare TiO2 nanoparticles (6 fmol). The urea-TiO2 could ionize proteins of more than 20 000 Da such as trypsinogen (600 fmol). (3) The urea modification of TiO2 had the advantage of selective detection of phosphopeptides without sample clean up, or prefractionation in tryptic digest products of bovine hemoglobin. Copyright (C) 2009 John Wiley & Sons, Ltd.

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