TY - JOUR
T1 - MALDI-MS imaging of features smaller than the size of the laser beam
AU - Jurchen, John C.
AU - Rubakhin, Stanislav S.
AU - Sweedler, Jonathan V.
N1 - Funding Information:
The authors thank Mr. Cory Scanlan for initial assistance in EM disk preparation, and Mr. Eric B. Monroe for assistance in figure preparation. JJ gratefully acknowledges support through an NRSA traineeship sponsored by the NIAAA 1F32 AA014459. This work was supported by NIH through DA14879 and the UIUC Neuroproteomics Center on Cell-Cell Signaling through grant P30 DA018310.
PY - 2005/10
Y1 - 2005/10
N2 - The feasibility of matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) imaging of features smaller than the laser beam size has been demonstrated. The method involves the complete ablation of the MALDI matrix coating the sample at each sample position and moving the sample target a distance less than the diameter of the laser beam before repeating the process. In the limit of complete sample ablation, acquiring signal from adjacent positions spaced by distances smaller than the sample probe enhances image resolution as the measured analyte signal only arises from the overlap of the laser beam size and the non-ablated sample surface. Image acquisition of features smaller than the laser beam size has been demonstrated with peptide standards deposited on electron microscopy calibration grids and with neuropeptides originating from single cells. The presented MS imaging technique enables ∼25 μm imaging spatial resolution using commercial MALDI mass spectrometers having irregular laser beam sizes of several hundred micron diameters. With appropriate sampling, the size of the laser beam is not a strict barrier to the attainable MALDI-MS imaging resolution.
AB - The feasibility of matrix-assisted laser desorption/ionization mass spectrometry (MALDI-MS) imaging of features smaller than the laser beam size has been demonstrated. The method involves the complete ablation of the MALDI matrix coating the sample at each sample position and moving the sample target a distance less than the diameter of the laser beam before repeating the process. In the limit of complete sample ablation, acquiring signal from adjacent positions spaced by distances smaller than the sample probe enhances image resolution as the measured analyte signal only arises from the overlap of the laser beam size and the non-ablated sample surface. Image acquisition of features smaller than the laser beam size has been demonstrated with peptide standards deposited on electron microscopy calibration grids and with neuropeptides originating from single cells. The presented MS imaging technique enables ∼25 μm imaging spatial resolution using commercial MALDI mass spectrometers having irregular laser beam sizes of several hundred micron diameters. With appropriate sampling, the size of the laser beam is not a strict barrier to the attainable MALDI-MS imaging resolution.
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U2 - 10.1016/j.jasms.2005.06.006
DO - 10.1016/j.jasms.2005.06.006
M3 - Article
C2 - 16095912
AN - SCOPUS:25144493577
SN - 1044-0305
VL - 16
SP - 1654
EP - 1659
JO - Journal of the American Society for Mass Spectrometry
JF - Journal of the American Society for Mass Spectrometry
IS - 10
ER -