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通过冷冻电子显微镜对多毛纲蠕虫庞贝蠕虫的巨型血红蛋白进行三维重建。

Three-dimensional reconstruction by cryoelectron microscopy of the giant hemoglobin of the polychaete worm Alvinella pompejana.

作者信息

de Haas F, Zal F, You V, Lallier F, Toulmond A, Lamy J N

机构信息

Groupe d'Analyse Structurale des Antigènes (URA 1334 CNRS), Tours, France.

出版信息

J Mol Biol. 1996 Nov 22;264(1):111-20. doi: 10.1006/jmbi.1996.0627.

Abstract

A frozen-hydrated specimen of the hexagonal bilayer hemoglobin (HBL Hb) from the deep-sea hydrothermal vent polychaete worm Alvinella pompejana, the most thermophilic metazoan known to date, was observed in the electron microscope and subjected to three-dimensional (3D) reconstruction by the method of random conical tilt series. At a resolution of 34.6 A by the differential phase residual method and 27.7 A by the Fourier shell correlation method, the 3D volume possesses a D6 point-group symmetry. While in previous 3D reconstructions of annelid and vestimentiferan Hbs the vertices of the upper layer were 16 degrees rotated compared with those of the lower layer, in Alvinella Hb the vertices of the two hexagonal layers are almost perfectly eclipsed when viewed along the 6-fold axis. As in the HBL Hbs of Riftia pachyptila and Macrobdella decora, a central linker complex is decorated by 12 hollow globular substructures (HGS). The linker complex comprises (1) a central hexagonal toroid, (2) two internal bracelets onto which the HGSs are built, and (3) six connections between the two hexagonal layers. Each HGS is composed of six masses, which are separated when the volume is displayed at high threshold, plus one additional mass involved in the bracelet connecting the six HGSs in both hexagonal layers. The HGSs have a local pseudo 3-fold symmetry and a disposition of the high-density masses different from those of Riftia V1 Hb.

摘要

从深海热液喷口多毛纲蠕虫庞贝蠕虫(Alvinella pompejana)中提取的六角双层血红蛋白(HBL Hb)的冷冻水合标本,该蠕虫是迄今为止已知的最嗜热的后生动物,在电子显微镜下进行了观察,并通过随机锥形倾斜系列方法进行了三维(3D)重建。通过差分相位残余法分辨率为34.6 Å,通过傅里叶壳相关法分辨率为27.7 Å,该3D体积具有D6点群对称性。在先前对环节动物和管栖蠕虫血红蛋白的3D重建中,上层的顶点与下层的顶点相比旋转了16度,而在庞贝蠕虫血红蛋白中,当沿六重轴观察时,两个六边形层的顶点几乎完全重叠。与厚壳贻贝(Riftia pachyptila)和美洲水蛭(Macrobdella decora)的HBL血红蛋白一样,一个中央连接复合体由12个空心球状亚结构(HGS)修饰。连接复合体包括:(1)一个中央六边形环面;(2)两个内部手镯,HGS构建在其上;(3)两个六边形层之间的六个连接。每个HGS由六个团块组成,当以高阈值显示体积时它们会分开,再加上一个额外的团块,参与连接两个六边形层中六个HGS的手镯。HGS具有局部伪三重对称性,并且高密度团块的排列与厚壳贻贝V1血红蛋白不同。

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