Therisod H, Labas V, Caroff M
Equipe Endotoxines, UMR 8619 du Centre National de la Recherche Scientifique, Biochimie, Université de Paris-Sud, Orsay, France.
Anal Chem. 2001 Aug 15;73(16):3804-7. doi: 10.1021/ac010313s.
A rapid method for the microscale extraction of lipopolysaccharides (endotoxins, LPSs) from rough-type Gram-negative bacteria was developed using thin-layer chromatography (TLC) combined with improved conditions for LPS analysis by mass spectrometry. TLC of intact bacteria on silica gel plates in an appropriate solvent selectively extracted and separated their LPS components. The bands of molecular species were scraped from the plates after nondestructive visualization, directly mixed with matrix, and analyzed by laser desorption time-of-flight mass spectrometry. Lipids A and Re-type LPSs were analyzed after transfer to a membrane. Adding citric acid to the matrix gave greatly improved mass spectra. The system allows characterization of bacterial LPS at the microscale level and is equally well applicable to heterogeneous LPS and lipid A preparations (Escherichia coli lipid A and Bordetella lipopolysaccharides were used). The technique provides a rapid determination of the heterogeneity of unmodified preparations and the determination of the molecular weight of each separated component.
开发了一种从粗糙型革兰氏阴性细菌中微量提取脂多糖(内毒素,LPS)的快速方法,该方法采用薄层色谱(TLC)并结合了改进的LPS质谱分析条件。在硅胶板上于适当溶剂中对完整细菌进行TLC,可选择性地提取并分离其LPS成分。在无损可视化后,从板上刮下分子种类的条带,直接与基质混合,并通过激光解吸飞行时间质谱进行分析。脂质A和Re型LPS在转移至膜上后进行分析。向基质中添加柠檬酸可大大改善质谱图。该系统能够在微量水平上对细菌LPS进行表征,同样适用于异质性LPS和脂质A制剂(使用了大肠杆菌脂质A和博德特氏菌脂多糖)。该技术可快速测定未修饰制剂的异质性,并确定每个分离成分的分子量。