TY - JOUR
T1 - High mass accuracy and high mass resolving power FT-ICR secondary ion mass spectrometry for biological tissue imaging
AU - Smith, D.F.
AU - Kiss, A.
AU - Leach, F.E.
AU - Robinson, E.W.
AU - Paša-Tolić, L.
AU - Heeren, R.M.A.
PY - 2013
Y1 - 2013
N2 - Biological tissue imaging by secondary ion mass
spectrometry has seen rapid development with the commercial
availability of polyatomic primary ion sources. Endogenous
lipids and other small bio-molecules can now be
routinely mapped on the sub-micrometer scale. Such experiments
are typically performed on time-of-flight mass spectrometers
for high sensitivity and high repetition rate
imaging. However, such mass analyzers lack the mass resolving
power to ensure separation of isobaric ions and the
mass accuracy for elemental formula assignment based on
exact mass measurement. We have recently reported a secondary
ion mass spectrometer with the combination of a C60
primary ion gun with a Fourier transform ion cyclotron
resonance mass spectrometer (FT-ICR MS) for high mass
resolving power, high mass measurement accuracy, and
tandem mass spectrometry capabilities. In this work, high
specificity and high sensitivity secondary ion FT-ICR MS
was applied to chemical imaging of biological tissue. An
entire rat brain tissue was measured with 150 μm spatial
resolution (75 μm primary ion spot size) with mass resolving
power (m/Δm50%) of 67,500 (at m/z 750) and rootmean-
square measurement accuracy less than two partsper-
million for intact phospholipids, small molecules and
fragments. For the first time, ultra-high mass resolving
power SIMS has been demonstrated, with m/Δm50%>
3,000,000. Higher spatial resolution capabilities of the platform
were tested at a spatial resolution of 20 μm. The results
represent order of magnitude improvements in mass resolving
power and mass measurement accuracy for SIMS imaging
and the promise of the platform for ultra-high mass
resolving power and high spatial resolution imaging.
AB - Biological tissue imaging by secondary ion mass
spectrometry has seen rapid development with the commercial
availability of polyatomic primary ion sources. Endogenous
lipids and other small bio-molecules can now be
routinely mapped on the sub-micrometer scale. Such experiments
are typically performed on time-of-flight mass spectrometers
for high sensitivity and high repetition rate
imaging. However, such mass analyzers lack the mass resolving
power to ensure separation of isobaric ions and the
mass accuracy for elemental formula assignment based on
exact mass measurement. We have recently reported a secondary
ion mass spectrometer with the combination of a C60
primary ion gun with a Fourier transform ion cyclotron
resonance mass spectrometer (FT-ICR MS) for high mass
resolving power, high mass measurement accuracy, and
tandem mass spectrometry capabilities. In this work, high
specificity and high sensitivity secondary ion FT-ICR MS
was applied to chemical imaging of biological tissue. An
entire rat brain tissue was measured with 150 μm spatial
resolution (75 μm primary ion spot size) with mass resolving
power (m/Δm50%) of 67,500 (at m/z 750) and rootmean-
square measurement accuracy less than two partsper-
million for intact phospholipids, small molecules and
fragments. For the first time, ultra-high mass resolving
power SIMS has been demonstrated, with m/Δm50%>
3,000,000. Higher spatial resolution capabilities of the platform
were tested at a spatial resolution of 20 μm. The results
represent order of magnitude improvements in mass resolving
power and mass measurement accuracy for SIMS imaging
and the promise of the platform for ultra-high mass
resolving power and high spatial resolution imaging.
U2 - 10.1007/s00216-013-7048-1
DO - 10.1007/s00216-013-7048-1
M3 - Article
SN - 1618-2642
VL - 405
SP - 6069
EP - 6076
JO - Analytical and Bioanalytical Chemistry
JF - Analytical and Bioanalytical Chemistry
ER -