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通过完整细胞基质辅助激光解吸电离傅里叶变换质谱法阐明脂质和磷脂化学的策略与数据分析技术

Strategies and data analysis techniques for lipid and phospholipid chemistry elucidation by intact cell MALDI-FTMS.

作者信息

Jones Jeffrey J, Stump Michael J, Fleming Richard C, Lay Jackson O, Wilkins Charles L

机构信息

Department of Chemistry and Biochemistry, University of Arkansas, Fayetteville, Arkansas 72701, USA.

出版信息

J Am Soc Mass Spectrom. 2004 Nov;15(11):1665-74. doi: 10.1016/j.jasms.2004.08.007.

DOI:10.1016/j.jasms.2004.08.007
PMID:15519235
Abstract

Ions attributed to lipids and phospholipids are directly observed by desorption from whole bacteria using intact cell (IC) matrix-assisted laser desorption-ionization (MALDI) Fourier transform mass spectrometry (FTMS). Saccharomyces cerevisiae are grown in rich media broth, concentrated, and applied directly to the MALDI surface without lysis or chemical treatment. FTMS of MALDI ions gives excellent signal to noise ratios with typical resolving powers of 90,000 and mass precision better than 0.002 Da. Use of accurate mass measurements and a simple set of rules allow assignment of major peaks into one of twelve expected lipid classes. Subsequently, fractional mass versus whole number mass plots are employed to enhance visual interpretation of the high-resolution data and to facilitate detection of related ions such as those representing homologous series or different degrees of unsaturation. This approach, coupled with rules based on bacterial biochemistry, is used to classify ions with m/z up to about 1000. Major spectral peaks in the range m/z 200-1000 are assigned as lipids and phospholipids. In this study, it is assumed that biologically-derived ions with m/z values lower than 1000 are lipids. This is not unreasonable in view of the facts that molecular weights of lipids are almost always less than 1000 Da, that the copy numbers for lipids in a cell are higher than those for any single protein or other component, and that lipids are generally collections of distinct homologous partners, unlike proteins or other cell components. This paper presents a new rapid lipid-profiling method based on IC MALDI-FTMS.

摘要

利用完整细胞(IC)基质辅助激光解吸电离(MALDI)傅里叶变换质谱(FTMS)从全菌中解吸,可直接观察到归因于脂质和磷脂的离子。酿酒酵母在丰富培养基肉汤中生长、浓缩,然后直接应用于MALDI表面,无需裂解或化学处理。MALDI离子的FTMS给出了优异的信噪比,典型分辨率为90,000,质量精度优于0.002 Da。使用精确质量测量和一组简单规则可将主要峰分配到十二种预期脂质类别之一。随后,利用分数质量与整数质量图来增强对高分辨率数据的视觉解释,并便于检测相关离子,如代表同系物系列或不同不饱和度的离子。这种方法与基于细菌生物化学的规则相结合,用于对质荷比高达约1000的离子进行分类。质荷比在200 - 1000范围内的主要光谱峰被指定为脂质和磷脂。在本研究中,假设质荷比低于1000的生物衍生离子为脂质。鉴于脂质的分子量几乎总是小于1000 Da、细胞中脂质的拷贝数高于任何单一蛋白质或其他成分的拷贝数,以及脂质通常是不同同源物的集合,而不像蛋白质或其他细胞成分,这种假设并非不合理。本文提出了一种基于IC MALDI - FTMS的新型快速脂质谱分析方法。

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