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T4 尾和尾丝的形态发生。

Morphogenesis of the T4 tail and tail fibers.

机构信息

Ecole Polytechnique Fédérale de Lausanne (EPFL), Institut de Physique des Systèmes Biologiques, BSP-415, CH-1015 Lausanne, Switzerland.

出版信息

Virol J. 2010 Dec 3;7:355. doi: 10.1186/1743-422X-7-355.

Abstract

Remarkable progress has been made during the past ten years in elucidating the structure of the bacteriophage T4 tail by a combination of three-dimensional image reconstruction from electron micrographs and X-ray crystallography of the components. Partial and complete structures of nine out of twenty tail structural proteins have been determined by X-ray crystallography and have been fitted into the 3D-reconstituted structure of the "extended" tail. The 3D structure of the "contracted" tail was also determined and interpreted in terms of component proteins. Given the pseudo-atomic tail structures both before and after contraction, it is now possible to understand the gross conformational change of the baseplate in terms of the change in the relative positions of the subunit proteins. These studies have explained how the conformational change of the baseplate and contraction of the tail are related to the tail's host cell recognition and membrane penetration function. On the other hand, the baseplate assembly process has been recently reexamined in detail in a precise system involving recombinant proteins (unlike the earlier studies with phage mutants). These experiments showed that the sequential association of the subunits of the baseplate wedge is based on the induced-fit upon association of each subunit. It was also found that, upon association of gp53 (gene product 53), the penultimate subunit of the wedge, six of the wedge intermediates spontaneously associate to form a baseplate-like structure in the absence of the central hub. Structure determination of the rest of the subunits and intermediate complexes and the assembly of the hub still require further study.

摘要

在过去的十年中,通过电子显微镜三维图像重建和组成成分的 X 射线晶体学的结合,在阐明噬菌体 T4 尾部结构方面取得了显著进展。通过 X 射线晶体学已经确定了 20 个尾部结构蛋白中的 9 个的部分和完整结构,并将其拟合到“延伸”尾部的三维重构结构中。“收缩”尾部的三维结构也已确定,并根据组成蛋白进行了解释。鉴于收缩前后的准原子尾部结构,现在可以根据亚基蛋白的相对位置变化来理解基板的大体构象变化。这些研究解释了基板构象变化和尾部收缩如何与尾部对宿主细胞的识别和膜穿透功能相关。另一方面,在一个涉及重组蛋白的精确系统中(与早期的噬菌体突变体研究不同),最近对基板组装过程进行了详细的重新检查。这些实验表明,基板楔形物亚基的顺序缔合是基于每个亚基缔合时的诱导契合。还发现,在 gp53(基因产物 53),楔形物的倒数第二个亚基,六个楔形物中间物在没有中心轮毂的情况下自发缔合形成类似基板的结构。其余亚基和中间复合物的结构确定以及轮毂的组装仍需要进一步研究。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4407/3004832/6c1c0cbba7b6/1743-422X-7-355-1.jpg

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