傅里叶变换离子回旋共振
化学
质谱法
质谱成像
子空间拓扑
吞吐量
接头(建筑物)
分辨率(逻辑)
时间分辨率
生物系统
图像分辨率
化学成像
傅里叶变换
分析化学(期刊)
算法
人工智能
计算机科学
光学
色谱法
高光谱成像
物理
工程类
建筑工程
生物
电信
量子力学
无线
作者
Yuxuan Richard Xie,Daniel C. Castro,Stanislav S. Rubakhin,Jonathan V. Sweedler,Fan Lam
标识
DOI:10.1021/acs.analchem.1c05279
摘要
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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