化学
质谱成像
反褶积
质谱法
电喷雾电离
定量分析(化学)
规范化(社会学)
样品制备
色谱法
马尔迪成像
定量蛋白质组学
蛋白质组学
信号(编程语言)
内生
基质辅助激光解吸/电离
解吸电喷雾电离
肽图谱
生物材料
生物组织
分析化学(期刊)
计算生物学
生物标本
分辨率(逻辑)
作者
Mushfeqa Iqfath,Andrew K. Swansiger,Manxi Yang,Lily Miller,Alyssa M. Moore,Emerson Hernly,Yunpeng Bai,Zhong-Yin Zhang,James S. Prell,Julia Laskin
标识
DOI:10.1021/acs.analchem.5c05187
摘要
Quantitative imaging of endogenous proteins in biological tissues is essential for understanding their roles in cellular signaling and metabolism. Mass spectrometry imaging (MSI) using nanospray desorption electrospray ionization (nano-DESI) is a label-free approach for mapping intact proteins in biological tissues with minimal sample preparation. However, signal suppression during ionization presents a challenge for quantification. In this study, we introduce a quantitative nano-DESI MSI approach by incorporating protein internal standards (IS) into the extraction solvent. Ion images were generated using iFAMS deconvolution software, which efficiently isolates protein-specific signals from a complex background. A systematic evaluation of normalization strategies indicates that accurate quantification in each pixel is achieved using charge-weighted signal normalization to the IS signal. We demonstrate quantitative imaging of endogenous proteins using only one IS and validate the approach using immunofluorescence imaging and bulk analysis. This robust approach enables accurate protein mapping and quantification in MSI experiments, providing deeper insights into protein function in complex biological systems.
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