Adjustable fragmentation in laser desorption/ionization from laser-induced silicon microcolumn arrays

被引:80
作者
Chen, Yong [1 ]
Vertes, Akos [1 ]
机构
[1] George Washington Univ, Dept Chem, Inst Prote Technol & Applicat, Washington, DC 20052 USA
关键词
D O I
10.1021/ac060405n
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Laser-induced silicon microcolumn arrays (LISMA) were developed as matrix-free substrates for soft laser desorption/ionization mass spectrometry (SLDI-MS). When low-resistivity silicon wafers were irradiated in air, sulfur hexafluoride, or water environment with multiple pulses from a 3 x omega mode-locked Nd:YAG laser, columnar structures were formed on the surface. The radii of curvature of the column tips varied with the processing environment, ranging from similar to 120 nm in water, to <1 mu m in SF6, and to similar to 2 mu m in air. In turn, these microcolumn arrays were used as matrix-free soft laser desorption substrates. In SLDI-MS experiments with a nitrogen laser, the microcolumn arrays obtained in water environment readily produced molecular ions for peptides and synthetic polymers at low laser fluence. These surfaces demonstrated the best ion yield among the three arrays. The threshold laser fluence and ion yield were comparable to those observed in matrix-assisted laser desorption/ionization. Low-femtomole sensitivity and similar to 6000 Da mass range were achieved. At elevated laser fluence, efficient in-source decay was observed and extensive peptide sequence information was extracted from the resulting mass spectra. The versatility of LISMA was attributed to confinement effects due to the submicrometer morphology and to the surface, thermal, and optical properties of processed silicon.
引用
收藏
页码:5835 / 5844
页数:10
相关论文
共 64 条
[1]   Proton nature of radiation-induced positive charge in SiO2 layers on Si [J].
Afanas'ev, VV ;
Stesmans, A .
EUROPHYSICS LETTERS, 2001, 53 (02) :233-239
[2]   On the mechanism of laser-induced desorption-ionization of organic compounds from etched silicon and carbon surfaces [J].
Alimpiev, S ;
Nikiforov, S ;
Karavanskii, V ;
Minton, T ;
Sunner, J .
JOURNAL OF CHEMICAL PHYSICS, 2001, 115 (04) :1891-1901
[3]   Integrated microfluidic system enabling (bio)chemical reactions with on-line MALDI-TOF mass spectrometry [J].
Brivio, M ;
Fokkens, RH ;
Verboom, W ;
Reinhoudt, DN ;
Tas, NR ;
Goedbloed, M ;
van den Berg, A .
ANALYTICAL CHEMISTRY, 2002, 74 (16) :3972-3976
[4]   Desorption/ionization mass spectrometry on nanocrystalline titania sol-gel-deposited films [J].
Chen, CT ;
Chen, YC .
RAPID COMMUNICATIONS IN MASS SPECTROMETRY, 2004, 18 (17) :1956-1964
[5]   Carbon nanotubes as affinity probes for peptides and proteins in MALDI MS analysis [J].
Chen, WY ;
Wang, LS ;
Chiu, HT ;
Chen, YC ;
Lee, CY .
JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 2004, 15 (11) :1629-1635
[6]   Pumping rate and surface morphology dependence of ionization processes in matrix-assisted laser desorption ionization [J].
Chen, Y ;
Vertes, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 2003, 107 (46) :9754-9761
[7]   Comparison of structure and properties of femtosecond and nanosecond laser-structured silicon [J].
Crouch, CH ;
Carey, JE ;
Warrender, JM ;
Aziz, MJ ;
Mazur, E ;
Génin, FY .
APPLIED PHYSICS LETTERS, 2004, 84 (11) :1850-1852
[8]   Desorption-ionization mass spectrometry using deposited nanostructured silicon films [J].
Cuiffi, JD ;
Hayes, DJ ;
Fonash, SJ ;
Brown, KN ;
Jones, AD .
ANALYTICAL CHEMISTRY, 2001, 73 (06) :1292-1295
[9]   Graphite/liquid mixed matrices for laser desorption/ionization mass spectrometry [J].
Dale, MJ ;
Knochenmuss, R ;
Zenobi, R .
ANALYTICAL CHEMISTRY, 1996, 68 (19) :3321-3329
[10]   Integrated microanalytical technology enabling rapid and automated protein identification [J].
Ekström, S ;
Önnerfjord, P ;
Nilsson, J ;
Bengtsson, M ;
Laurell, T ;
Marko-Varga, G .
ANALYTICAL CHEMISTRY, 2000, 72 (02) :286-293