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脂多糖双层结构:化学型、核心突变、二价阳离子及温度的影响

Lipopolysaccharide bilayer structure: effect of chemotype, core mutations, divalent cations, and temperature.

作者信息

Snyder S, Kim D, McIntosh T J

机构信息

Department of Cell Biology, Duke University Medical Center, Durham, North Carolina 27710, USA.

出版信息

Biochemistry. 1999 Aug 17;38(33):10758-67. doi: 10.1021/bi990867d.

Abstract

Lipopolysaccharide (LPS), the primary lipid on the surface of Gram-negative bacteria, is thought to act as a protective and permeability barrier. X-ray diffraction analysis of osmotically stressed LPS multilayers was used to determine the structure and interactive properties of LPSs from strains containing the minimum number of sugars necessary for bacterial survival (Re chemotype) to the maximum number of sugars found in rough bacteria (Ra chemotype). At 20 degrees C in the absence of divalent cations, LPS suspensions gave a sharp wide-angle reflection at 4.23 A and a broad low-angle band centered at 50-68 A depending on the chemotype, indicating the presence of gel phase bilayers separated by large fluid spaces. As osmotic pressure was applied, the apposing bilayers were squeezed together and lamellar diffraction at 6 A resolution was obtained. At low applied pressures (<10(6) dyn/cm2), the total repulsive pressure between bilayers could be explained by electrostatic double layer theory. At higher applied pressures, there was a sharp upward break in each pressure-distance relation, indicating the presence of a hydrophilic steric barrier whose range depended strongly on the LPS chemotype. The positions of these upward breaks, along with electron density profiles, showed that the sugar core width systematically increased from 10 A for the Re chemotype to 27 A for the Ra chemotype. In excess buffer, the addition of divalent cations brought the bilayers into steric contact. Electron density profiles were used to determine the locations of cation binding sites and polar substituents on the LPS oligosaccharide core. The area per hydrocarbon chain was approximately 26 A2 in liquid-crystalline LPS bilayers, an indication of an acyl chain packing that is much tighter than that found in bilayers composed of typical membrane lipids. This unusually tight packing could be a critical factor in the permeability barrier provided by LPS.

摘要

脂多糖(LPS)是革兰氏阴性菌表面的主要脂质,被认为起到保护和渗透屏障的作用。对经渗透压应激的LPS多层膜进行X射线衍射分析,以确定从含有细菌存活所需最少糖数的菌株(Re化学型)到粗糙细菌中发现的最多糖数的菌株(Ra化学型)的LPS的结构和相互作用特性。在20摄氏度且不存在二价阳离子的情况下,LPS悬浮液在4.23 Å处给出一个尖锐的广角反射,以及一个根据化学型不同而以50 - 68 Å为中心的宽低角度带,这表明存在由大的流体空间分隔的凝胶相双层膜。当施加渗透压时,相对的双层膜被挤压在一起,并获得了6 Å分辨率的层状衍射。在低施加压力(<10⁶ dyn/cm²)下,双层膜之间的总排斥压力可以用静电双层理论来解释。在较高施加压力下,每个压力 - 距离关系中都有一个急剧的向上转折,表明存在一个亲水性空间位垒,其范围强烈依赖于LPS化学型。这些向上转折的位置以及电子密度分布表明,糖核心宽度从Re化学型的10 Å系统地增加到Ra化学型的27 Å。在过量缓冲液中,添加二价阳离子使双层膜进入空间接触。电子密度分布被用于确定LPS寡糖核心上阳离子结合位点和极性取代基的位置。在液晶态LPS双层膜中,每个烃链的面积约为26 Ų,这表明酰基链的堆积比由典型膜脂组成的双层膜中发现的堆积要紧密得多。这种异常紧密的堆积可能是LPS提供渗透屏障的关键因素。

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