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尾形态控制着具有一个脂多糖受体识别系统的两种沙门氏菌噬菌体的 DNA 释放。

Tail morphology controls DNA release in two Salmonella phages with one lipopolysaccharide receptor recognition system.

机构信息

Physikalische Biochemie, Universität Potsdam, Karl-Liebknecht-Str. 24-25, 14476 Potsdam, Germany.

出版信息

Mol Microbiol. 2012 Mar;83(6):1244-53. doi: 10.1111/j.1365-2958.2012.08006.x. Epub 2012 Feb 27.

Abstract

Bacteriophages use specific tail proteins to recognize host cells. It is still not understood to molecular detail how the signal is transmitted over the tail to initiate infection. We have analysed in vitro DNA ejection in long-tailed siphovirus 9NA and short-tailed podovirus P22 upon incubation with Salmonella typhimurium lipopolysaccharide (LPS). We showed for the first time that LPS alone was sufficient to elicit DNA release from a siphovirus in vitro. Crystal structure analysis revealed that both phages use similar tailspike proteins for LPS recognition. Tailspike proteins hydrolyse LPS O antigen to position the phage on the cell surface. Thus we were able to compare in vitro DNA ejection processes from two phages with different morphologies with the same receptor under identical experimental conditions. Siphovirus 9NA ejected its DNA about 30 times faster than podovirus P22. DNA ejection is under control of the conformational opening of the particle and has a similar activation barrier in 9NA and P22. Our data suggest that tail morphology influences the efficiencies of particle opening given an identical initial receptor interaction event.

摘要

噬菌体利用特定的尾部蛋白识别宿主细胞。目前仍不清楚信号是如何通过尾部传递从而启动感染的,其分子细节尚不清楚。我们分析了长尾丝状噬菌体 9NA 和短尾痘病毒 P22 在与鼠伤寒沙门氏菌脂多糖(LPS)孵育时的体外 DNA 喷射。我们首次表明,LPS 本身足以在体外从丝状噬菌体中引发 DNA 释放。晶体结构分析表明,两种噬菌体都使用类似的尾刺蛋白来识别 LPS。尾刺蛋白将 LPS O 抗原水解,从而将噬菌体定位在细胞表面。因此,我们能够在相同的实验条件下,用相同的受体比较两种具有不同形态的噬菌体的体外 DNA 喷射过程。丝状噬菌体 9NA 的 DNA 喷射速度比痘病毒 P22 快约 30 倍。DNA 喷射受颗粒构象开放的控制,在 9NA 和 P22 中具有相似的激活势垒。我们的数据表明,在相同的初始受体相互作用事件下,尾部形态会影响颗粒开口的效率。

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