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胡萝卜软腐欧文氏菌脂多糖中脂质A组分的物理化学分析及其生物活性

Physico-chemical analysis of lipid A fractions of lipopolysaccharide from Erwinia carotovora in relation to bioactivity.

作者信息

Fukuoka S, Brandenburg K, Müller M, Lindner B, Koch M H, Seydel U

机构信息

Shikoku National Industrial Research Institute, Takamatsu, Japan.

出版信息

Biochim Biophys Acta. 2001 Feb 9;1510(1-2):185-97. doi: 10.1016/s0005-2736(00)00347-3.

Abstract

Highly purified bisphosphoryl, monophosphoryl and dephosphoryl lipids A from Erwinia carotovora with different acylation patterns were characterized physico-chemically. Applying matrix assisted laser desorption/ionization mass spectrometry, the purity of the lipid A fractions was determined, and from monolayer measurements the molecular space requirement was estimated. Fourier transform infrared spectroscopy allowed the elucidation of the gel to liquid crystalline phase transition of the acyl chains as well as the determination of the tilt angle of the diglucosamine backbone with respect to the acyl chain direction applying dichroitic measurements with attenuated total reflectance. With synchrotron radiation small-angle X-ray diffraction the supramolecular aggregate structure was determined, and with fluorescence resonance energy transfer spectroscopy the lipopolysaccharide binding protein induced intercalation of lipid A into a phospholipid matrix corresponding to that of the macrophage membrane was investigated. From the results, a clear dependence of the physico-chemical parameters on the particular lipid A structure can be followed. Furthermore, these parameters correlate well with the biological activities of the various lipids A as deduced from their ability to induce biological activity (Limulus assay and cytokine induction in mononuclear cells). These results contribute to a closer interpretation of the physico-chemical prerequisites for endotoxic activity as found for enterobacterial lipid A.

摘要

对来自胡萝卜软腐欧文氏菌的具有不同酰化模式的高纯度双磷酸化、单磷酸化和去磷酸化脂多糖A进行了物理化学表征。应用基质辅助激光解吸/电离质谱法测定了脂多糖A组分的纯度,并通过单层测量估算了分子空间需求。傅里叶变换红外光谱法能够阐明酰基链从凝胶相到液晶相的转变,以及通过衰减全反射二向色性测量确定二葡糖胺主链相对于酰基链方向的倾斜角。利用同步辐射小角X射线衍射确定了超分子聚集体结构,并通过荧光共振能量转移光谱法研究了脂多糖结合蛋白诱导脂多糖A插入与巨噬细胞膜相对应的磷脂基质中的情况。从结果可以看出,物理化学参数明显依赖于特定的脂多糖A结构。此外,这些参数与从其诱导生物活性的能力(鲎试剂法和单核细胞中细胞因子诱导)推断出的各种脂多糖A的生物活性密切相关。这些结果有助于更深入地解释肠杆菌脂多糖A的内毒素活性的物理化学先决条件。

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