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Progress in Detection and Structural Characterization of Glycosphingolipids in Crude Lipid Extracts by Enzymatic Phospholipid Disintegration Combined with Thin-Layer Chromatography Immunodetection and IR-MALDI Mass Spectrometry

机译:酶磷脂分解-薄层色谱免疫检测-IR-MALDI质谱联用检测粗脂质提取物中糖鞘脂的结构特征

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In order to proceed in detection and structural analysis of glycosphingolipids (GSLs) in crude lipid extracts, which still remains a challenge in glycosphingolipidomics, we developed a strategy to structurally characterize neutral GSLs in total lipid extracts prepared from in vitro propagated human monocytic THP-1 cells, which were used as a model cell line. The procedure divides into (1) extraction of total lipids from cellular material, (2) enzymatical disintegration of phospholipids by treatment of the crude lipid extract with phospholipase C, (3) subsequent multiple thin-layer chromatography (TLC) overlay detection of individual GSLs with a mixture of various anti-GSL antibodies, and (4) structural analysis of immunostained GSLs directly on the TLC plate using infrared matrix-assisted laser desorption/ionization orthogonal time-of-flight mass spectrometry (IR-MALDI-o-TOF MS) in combination with collision-induced dissociation (CID). Whereas GSLs were mostly undetectable in untreated crude lipid extracts, pretreatment with phospholipase C resulted in clear-cut mass spectra. MS~1 and MS~2 analysis gave similar results when compared to those obtained with a highly purified neutral GSL preparation of THP-1 cells, which served as a control. We could demonstrate in this study the feasibility of simultaneous multiple immunodetection of individual neutral GSLs in one and the same TLC run and their structural characterization in crude lipid extracts after phospholipase C treatment, thereby avoiding laborious and long-lasting sample purification. This powerful combinatorial technique allows for efficient structural characterization of GSLs in small tissue samples and takes a step forward in the emerging field of glycosphingolipidomics.
机译:为了进行粗脂质提取物中糖鞘脂(GSLs)的检测和结构分析,糖脂鞘脂学仍然是一个挑战,我们开发了一种策略来表征从体外繁殖的人单核细胞THP-1制备的总脂质提取物中的中性GSLs细胞,用作模型细胞系。该程序分为(1)从细胞材料中提取总脂质,(2)通过用磷脂酶C处理粗脂质提取物来酶促分解磷脂,(3)随后对各个GSL进行多重薄层色谱(TLC)覆盖检测(5)使用红外基质辅助激光解吸/电离正交飞行时间质谱(IR-MALDI-o-TOF MS)在TLC板上直接对免疫染色的GSL进行结构分析)与碰撞诱导解离(CID)结合使用。尽管在未处理的粗脂质提取物中大部分检测不到GSL,但用磷脂酶C预处理可得到清晰的质谱图。与使用THP-1细胞的高纯度中性GSL制备物(作为对照)相比,MS_1和MS_2分析得出的结果相似。在这项研究中,我们可以证明在一次和相同的TLC运行中同时对单个中性GSL进行多次免疫检测的可行性,以及在磷脂酶C处理后粗脂质提取物中它们的结构表征,从而避免了费力且持久的样品纯化。这种强大的组合技术可对小组织样本中的GSL进行有效的结构表征,并在新兴的糖鞘脂系统学领域迈出了一步。

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