Department of Chemistry, ‡Department of Biochemistry, and §Department of Anatomy and Cell Biology, The University of Western Ontario , London, Ontario, Canada.
Anal Chem. 2017 Dec 5;89(23):12828-12836. doi: 10.1021/acs.analchem.7b03284. Epub 2017 Nov 15.
1,6-Diphenyl-1,3,5-hexatriene (DPH) is a commonly used fluorescence probe for studying cell membrane-lipids due to its affinity toward the acyl chains in the phospholipid bilayers. In this work, we investigated its use in matrix-assisted laser desorption/ionization (MALDI) as a new matrix for mass spectrometry imaging (MSI) of mouse and rat brain tissue. DPH exhibits very minimal matrix-induced background signals for the analysis of small molecules (below m/z of 1000). In the negative ion mode, DPH permits the highly sensitive detection of small fatty acids (m/z 200-350) as well as a variety of large lipids up to m/z of 1000, including lyso-phospholipid, phosphatidic acid (PA), phosphoethanolamine (PE), phosphatidylserine (PS), phosphatidylglycerol (PG), phosphatidylinositol (PI), and sulfatides (ST). The analytes were mostly detected as the deprotonated ion [M - H]. Our results also demonstrate that sublimated DPH is stable for at least 24 h under the vacuum of our MALDI mass spectrometer. The ability to apply DPH via sublimation coupled with its low volatility allows us to perform tissue imaging of the above analytes at high spatial resolution. The degree of lipid fragmentation was determined experimentally at varying laser intensities. The results illustrated that the use of relatively low laser energy is important to minimize the artificially generated fatty acid signals. On the other hand, the lipid fragmentation obtained at higher laser energies provided tandem MS information useful for lipid structure elucidation.
1,6-二苯基-1,3,5-己三烯(DPH)是一种常用于研究细胞膜脂质的荧光探针,因为它对磷脂双分子层中的酰基链具有亲和力。在这项工作中,我们研究了它在基质辅助激光解吸/电离(MALDI)中的用途,作为用于小鼠和大鼠脑组织质谱成像(MSI)的新基质。DPH 在分析小分子(低于 m/z 1000)时表现出非常低的基质诱导背景信号。在负离子模式下,DPH 允许对小脂肪酸(m/z 200-350)以及各种大脂质(高达 m/z 1000)进行高灵敏度检测,包括溶血磷脂、磷脂酸(PA)、磷酸乙醇胺(PE)、磷脂酰丝氨酸(PS)、磷脂酰甘油(PG)、磷脂酰肌醇(PI)和硫酸脂(ST)。分析物主要以去质子化离子[M-H]的形式检测到。我们的结果还表明,在我们的 MALDI 质谱仪的真空下,升华的 DPH 至少稳定 24 小时。通过升华施加 DPH 的能力及其低挥发性允许我们以高空间分辨率对上述分析物进行组织成像。通过在不同激光强度下进行实验确定了脂质碎裂的程度。结果表明,使用相对较低的激光能量对于最小化人为产生的脂肪酸信号很重要。另一方面,在较高激光能量下获得的脂质碎裂提供了用于脂质结构阐明的串联 MS 信息。