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首页> 外文期刊>Rapid Communications in Mass Spectrometry: RCM >A rapid one-step method for the characterization of membrane lipid remodeling in Francisella using matrix-assisted laser desorption ionization time-of-flight tandem mass spectrometry
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A rapid one-step method for the characterization of membrane lipid remodeling in Francisella using matrix-assisted laser desorption ionization time-of-flight tandem mass spectrometry

机译:基质辅助激光解吸电离飞行时间串联质谱法快速鉴定弗氏杆菌中膜脂质重塑的一步法

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摘要

Lipids are essential components of all bacterial membranes. The most common membrane-associated lipids in Gram-negative bacteria are phospholipids and lipid A, the hydrophobic anchor of lipopolysaccharide. Diversity in these lipids arises through structural modifications that include changes in the length and location of fatty acids, and the addition of phosphate and carbohydrate moieties. Analysis of individual structural modifications normally requires large quantities of starting material and multiple methods for the isolation, hydrolysis, and analysis. In this study, we developed a novel one-step protocol for the combined isolation of phospholipids and lipid A from Francisella subspecies followed by analysis using matrix-assisted laser desorption ionization time-of-flight tandem mass spectrometry. The total time for lipid isolation and analysis was approximately 15 min and with a lower limit of detection of approximately 100 ng of purified lipid. This protocol identified the major lipid structures using both wild-type Ft subspecies strains and lipid A biosynthesis mutants. We also determined the relative levels of individual lipid A and phospholipids after growth under conditions that mimic the mammalian infection process. This analysis showed that the bacterial membranes remodeled rapidly to adapt to changes in environmental growth conditions and may be important for Francisella pathogenesis.
机译:脂质是所有细菌膜必不可少的成分。革兰氏阴性细菌中最常见的与膜相关的脂质是磷脂和脂质A(脂多糖的疏水锚)。这些脂质的多样性是通过结构修饰而产生的,这些修饰包括改变脂肪酸的长度和位置,以及添加磷酸盐和碳水化合物部分。单个结构修饰的分析通常需要大量的原材料和多种方法进行分离,水解和分析。在这项研究中,我们开发了一种新的一步步骤,用于从弗氏杆菌亚种中分离分离磷脂和脂质A,然后使用基质辅助激光解吸电离飞行时间串联质谱进行分析。脂质分离和分析的总时间约为15分钟,检测下限约为100 ng纯化脂质。该协议使用野生型Ft亚种菌株和脂质A生物合成突变体鉴定了主要的脂质结构。我们还确定了在模拟哺乳动物感染过程的条件下生长后单个脂质A和磷脂的相对水平。该分析表明细菌膜迅速重塑以适应环境生长条件的变化,并且对于弗朗西斯菌的发病机理可能很重要。

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