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噬菌体P22形态发生过程中新包装DNA稳定化的步骤。

Steps in the stabilization of newly packaged DNA during phage P22 morphogenesis.

作者信息

Strauss H, King J

出版信息

J Mol Biol. 1984 Feb 5;172(4):523-43. doi: 10.1016/s0022-2836(84)80021-2.

Abstract

The protein products of three adjacent P22 genes, 4, 10 and 26, are required for the stabilization of DNA newly packaged into P22 phage capsids. We have isolated unstable DNA containing capsids from cells infected with mutants defective in these genes. All three classes could be converted into mature phage in vitro, confirming that they represent intermediates in particle maturation. The first of the three proteins to add to the newly filled capsids is gp4, followed by gp10 and gp26. The active form of gp4 sediments at 3 S, while the active forms of both gp10 and gp26 sediment at 5 S. These soluble subunits appear to polymerize onto the newly filled capsids to form the neck of the mature phage, the channel for DNA injection. Since gp4 is the first protein to act after DNA packaging, the unstable DNA containing capsids from 4- -infected cells must represent the direct product of the packaging of DNA into procapsids. The major fraction of these capsids lost activity with a half-life of 1.1 minutes at 23 degrees C, though they were much more stable at 0 degree C. Electron microscopic observations indicated that the loss of activity was due to the DNA exiting from the incomplete capsids. The marginal stability of the condensed DNA molecules within capsids is consistent with models of ATP-driven condensation and spontaneous DNA ejection. The basis of the stability of these highly condensed molecules remains to be determined.

摘要

三个相邻的P22基因(4、10和26)的蛋白质产物对于稳定新包装到P22噬菌体衣壳中的DNA是必需的。我们从感染了这些基因有缺陷的突变体的细胞中分离出了含有不稳定DNA的衣壳。所有这三类衣壳在体外都可以转化为成熟噬菌体,这证实它们代表了颗粒成熟过程中的中间体。三种蛋白质中首先添加到新填充衣壳上的是gp4,其次是gp10和gp26。gp4的活性形式沉降系数为3 S,而gp10和gp26的活性形式沉降系数均为5 S。这些可溶性亚基似乎聚合到新填充的衣壳上,形成成熟噬菌体的颈部,即DNA注入的通道。由于gp4是DNA包装后第一个起作用的蛋白质,因此来自感染4-突变体的细胞中含有不稳定DNA的衣壳必定代表了DNA包装到原衣壳中的直接产物。这些衣壳的主要部分在23℃下以1.1分钟的半衰期丧失活性,不过它们在0℃时要稳定得多。电子显微镜观察表明,活性丧失是由于DNA从不完整的衣壳中逸出。衣壳内浓缩DNA分子的边缘稳定性与ATP驱动的浓缩和自发DNA喷射模型一致。这些高度浓缩分子稳定性的基础仍有待确定。

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