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西亚试剂：Clathrate nanostructures for mass spectrometry

Clathrate nanostructures for mass spectrometry

Trent R. Northen1,2,6, Oscar Yanes1,2,6, Michael T. Northen4, Dena Marrinucci3, Winnie Uritboonthai1,2, Junefredo Apon1,2, Stephen L. Golledge5, Anders Nordström1,2 & Gary Siuzdak1,2,6

  1. Department of Molecular Biology,
  2. Scripps Center for Mass Spectrometry,
  3. Department of Cell Biology, The Scripps Research Institute, La Jolla, California 92037, USA
  4. Materials Department, University of California at Santa Barbara, Santa Barbara, California 93106, USA
  5. CAMCOR Surface Analysis Facility at the University of Oregon, Eugene, Oregon 97403, USA
  6. These authors contributed equally to this work.

Correspondence to: Gary Siuzdak1,2,6 Correspondence and requests for materials should be addressed to G.S. (Email: siuzdak@scripps.edu).

The ability of mass spectrometry to generate intact biomolecular ions efficiently in the gas phase has led to its widespread application in metabolomics1, proteomics2, biological imaging3, biomarker discovery4 and clinical assays (namely neonatal screens5). Matrix-assisted laser desorption/ionization6, 7 (MALDI) and electrospray ionization8 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 size9 (typically more than 10 mum), sensitivity and detection of small compounds (less than 500 Da). Secondary-ion mass spectrometry10 has extremely high lateral resolution (100 nm) and has found biological applications11, 12 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.