TY - JOUR
T1 - Enhancing the Throughput of FT Mass Spectrometry Imaging Using Joint Compressed Sensing and Subspace Modeling
AU - Xie, Yuxuan Richard
AU - Castro, Daniel C.
AU - Rubakhin, Stanislav S.
AU - Sweedler, Jonathan V.
AU - Lam, Fan
N1 - This project was supported by the National Institute on Drug Abuse under award No. P30DA018310, the National Human Genome Research Institute under award No. RM1HG010023 and National Institute of General Medical Sciences under award No. 1R35GM142969-01. Y.R.X acknowledges support from the Beckman Graduate Fellowship. The content is solely the responsibility of the authors and does not necessarily represent the official views of the awarding agencies.
PY - 2022/4/5
Y1 - 2022/4/5
N2 - Mass spectrometry imaging (MSI) allows for untargeted mapping of the chemical composition of tissues with attomole detection limits. MSI using Fourier transform (FT)-based mass spectrometers, such as FT-ion cyclotron resonance (FT-ICR), grants the ability to examine the chemical space with unmatched mass resolution and mass accuracy. However, direct imaging of large tissue samples using FT-ICR is slow. In this work, we present an approach that combines the subspace modeling of ICR temporal signals with compressed sensing to accelerate high-resolution FT-ICR MSI. A joint subspace and spatial sparsity constrained model computationally reconstructs high-resolution MSI data from the sparsely sampled transients with reduced duration, allowing a significant reduction in imaging time. Simulation studies and experimental implementation of the proposed method in investigation of brain tissues demonstrate a 10-fold enhancement in throughput of FT-ICR MSI, without the need for instrumental or hardware modifications.
AB - Mass spectrometry imaging (MSI) allows for untargeted mapping of the chemical composition of tissues with attomole detection limits. MSI using Fourier transform (FT)-based mass spectrometers, such as FT-ion cyclotron resonance (FT-ICR), grants the ability to examine the chemical space with unmatched mass resolution and mass accuracy. However, direct imaging of large tissue samples using FT-ICR is slow. In this work, we present an approach that combines the subspace modeling of ICR temporal signals with compressed sensing to accelerate high-resolution FT-ICR MSI. A joint subspace and spatial sparsity constrained model computationally reconstructs high-resolution MSI data from the sparsely sampled transients with reduced duration, allowing a significant reduction in imaging time. Simulation studies and experimental implementation of the proposed method in investigation of brain tissues demonstrate a 10-fold enhancement in throughput of FT-ICR MSI, without the need for instrumental or hardware modifications.
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U2 - 10.1021/acs.analchem.1c05279
DO - 10.1021/acs.analchem.1c05279
M3 - Article
C2 - 35324161
AN - SCOPUS:85127549511
SN - 0003-2700
VL - 94
SP - 5335
EP - 5343
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 13
ER -