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人源MD-2及其与抗内毒素脂质IVa复合物的晶体结构。

Crystal structures of human MD-2 and its complex with antiendotoxic lipid IVa.

作者信息

Ohto Umeharu, Fukase Koichi, Miyake Kensuke, Satow Yoshinori

机构信息

Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

Science. 2007 Jun 15;316(5831):1632-4. doi: 10.1126/science.1139111.

Abstract

Endotoxic lipopolysaccharide (LPS) with potent immunostimulatory activity is recognized by the receptor complex of MD-2 and Toll-like receptor 4. Crystal structures of human MD-2 and its complex with the antiendotoxic tetra-acylated lipid A core of LPS have been determined at 2.0 and 2.2 angstrom resolutions, respectively. MD-2 shows a deep hydrophobic cavity sandwiched by two beta sheets, in which four acyl chains of the ligand are fully confined. The phosphorylated glucosamine moieties are located at the entrance to the cavity. These structures suggest that MD-2 plays a principal role in endotoxin recognition and provide a basis for antiseptic drug development.

摘要

具有强大免疫刺激活性的内毒素脂多糖(LPS)被MD-2和Toll样受体4的受体复合物识别。人MD-2及其与LPS的抗内毒素四酰化脂质A核心的复合物的晶体结构分别在2.0和2.2埃分辨率下测定。MD-2显示出一个被两个β折叠夹在中间的深疏水腔,配体的四个酰基链完全被限制在其中。磷酸化的葡糖胺部分位于腔的入口处。这些结构表明MD-2在内毒素识别中起主要作用,并为抗菌药物开发提供了基础。

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