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1.
Nature ; 449(7165): 1033-6, 2007 Oct 25.
Article in English | MEDLINE | ID: mdl-17960240

ABSTRACT

The ability of mass spectrometry to generate intact biomolecular ions efficiently in the gas phase has led to its widespread application in metabolomics, proteomics, biological imaging, biomarker discovery and clinical assays (namely neonatal screens). Matrix-assisted laser desorption/ionization (MALDI) and electrospray ionization have been at the forefront of these developments. However, matrix application complicates the use of MALDI for cellular, tissue, biofluid and microarray analysis and can limit the spatial resolution because of the matrix crystal size (typically more than 10 mum), sensitivity and detection of small compounds (less than 500 Da). Secondary-ion mass spectrometry has extremely high lateral resolution (100 nm) and has found biological applications although the energetic desorption/ionization is a limitation owing to molecular fragmentation. Here we introduce nanostructure-initiator mass spectrometry (NIMS), a tool for spatially defined mass analysis. NIMS uses 'initiator' molecules trapped in nanostructured surfaces or 'clathrates' to release and ionize intact molecules adsorbed on the surface. This surface responds to both ion and laser irradiation. The lateral resolution (ion-NIMS about 150 nm), sensitivity, matrix-free and reduced fragmentation of NIMS allows direct characterization of peptide microarrays, direct mass analysis of single cells, tissue imaging, and direct characterization of blood and urine.


Subject(s)
Mass Spectrometry/instrumentation , Mass Spectrometry/methods , Nanostructures , Adsorption , Animals , Blood Chemical Analysis , Breast Neoplasms/chemistry , Breast Neoplasms/pathology , Cell Line, Tumor , Embryo, Mammalian/chemistry , Ions/chemistry , Lasers , Mice , Microscopy, Electron, Scanning , Nanostructures/chemistry , Protein Array Analysis , Sensitivity and Specificity , Urine/chemistry
2.
J Am Soc Mass Spectrom ; 18(11): 1945-9, 2007 Nov.
Article in English | MEDLINE | ID: mdl-17881245

ABSTRACT

The surface structure of porous silicon used in desorption/ionization on porous silicon (DIOS) mass analysis is known to play a primary role in the desorption/ionization (D/I) process. In this study, mass spectrometry and scanning electron microscopy (SEM) are used to examine the correlation between intact ion generation with surface ablation and surface morphology. The DIOS process is found to be highly laser energy dependent and correlates directly with the appearance of surface ions (Si(n)(+) and OSiH(+)). A threshold laser energy for DIOS is observed (10 mJ/cm(2)), which supports that DIOS is driven by surface restructuring and is not a strictly thermal process. In addition, three DIOS regimes are observed that correspond to surface restructuring and melting. These results suggest that higher surface area silicon substrates may enhance DIOS performance. A recent example that fits into this mechanism is the surface of silicon nanowires, which has a high surface energy and concomitantly requires lower laser energy for analyte desorption.


Subject(s)
Microscopy, Electron, Scanning , Silicon/chemistry , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization , Ions , Lasers , Nanotechnology , Porosity , Surface Properties
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