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盐掺杂与基质升华联用实现中性脂质的高空间分辨率 MALDI 成像质谱分析。

Combining Salt Doping and Matrix Sublimation for High Spatial Resolution MALDI Imaging Mass Spectrometry of Neutral Lipids.

机构信息

Mass Spectrometry Research Center , Vanderbilt University , 465 21st Ave S #9160 , Nashville , Tennessee 37235 , United States.

Department of Biochemistry , Vanderbilt University , 607 Light Hall , Nashville , Tennessee 37205 , United States.

出版信息

Anal Chem. 2019 Oct 15;91(20):12928-12934. doi: 10.1021/acs.analchem.9b02974. Epub 2019 Sep 23.

DOI:10.1021/acs.analchem.9b02974
PMID:31483620
Abstract

The combination of sodium salt doping of a tissue section along with the sublimation of the matrix 2,5-dihydrobenzoic acid (DHB) was found to be an effective coating for the simultaneous detection of neutral lipids and phospholipids using matrix-assisted laser desorption/ionization (MALDI) imaging mass spectrometry in positive ionization mode. Lithium, sodium, and potassium acetate were initially screened for their ability to cationize difficult to analyze neutral lipids such as cholesterol esters, cerebrosides, and triglycerides directly from a tissue section. The combination of sodium salt and DHB sublimation was found to be an effective cation/matrix combination for detection of neutral lipids. Further experimental optimizations revealed that sodium carbonate or sodium phosphate followed by DHB sublimation increases the signal intensity of the neutral lipids studied depending on the specific lipid family and tissue type by 10-fold to 140-fold compared with that of previously published methods. Application of sodium carbonate tissue doping and DHB sublimation resulted in crystal sizes ≤2 μm. We were thus able to image a mouse brain cerebellum at a high spatial resolution and detected 37 cerebrosides in a single run using a MALDI-TOF instrument. The combination of sodium doping and DHB sublimation offer a targeted and sensitive approach for the detection of neutral lipids that do not typically ionize well under normal MALDI conditions.

摘要

研究发现,对组织切片进行钠盐掺杂并升华基质 2,5-二羟基苯甲酸(DHB),是一种有效方法,可用于在正离子化模式下使用基质辅助激光解吸/电离(MALDI)成像质谱法同时检测中性脂质和磷脂。最初筛选了锂盐、钠盐和钾盐,以评估它们是否能直接从组织切片中阳离子化难以分析的中性脂质,如胆固醇酯、脑苷脂和甘油三酯。结果发现,钠盐和 DHB 升华的组合是一种有效的阳离子/基质组合,可用于检测中性脂质。进一步的实验优化表明,与先前发表的方法相比,碳酸钠或磷酸钠随后进行 DHB 升华,可根据特定脂质家族和组织类型,将研究的中性脂质的信号强度提高 10 到 140 倍。碳酸钠组织掺杂和 DHB 升华的应用导致晶体尺寸≤2μm。因此,我们能够在高空间分辨率下对小鼠大脑小脑进行成像,并使用 MALDI-TOF 仪器在单次运行中检测到 37 种脑苷脂。钠离子掺杂和 DHB 升华的组合为检测通常在常规 MALDI 条件下不易离子化的中性脂质提供了一种靶向且灵敏的方法。

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