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A negative staining method for high resolution electron microscopy of viruses.一种用于病毒高分辨率电子显微镜观察的负染色方法。
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Contribution of DNA conformation and topology in right-handed DNA wrapping by the Bacillus subtilis LrpC protein.枯草芽孢杆菌LrpC蛋白对右手DNA包裹中DNA构象和拓扑结构的贡献。
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The Sulfolobus solfataricus Lrp-like protein LysM regulates lysine biosynthesis in response to lysine availability.嗜热栖热菌Lrp样蛋白LysM可根据赖氨酸的可利用性调节赖氨酸的生物合成。
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Leucine-regulated self-association of leucine-responsive regulatory protein (Lrp) from Escherichia coli.来自大肠杆菌的亮氨酸响应调节蛋白(Lrp)的亮氨酸调节的自我缔合。
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Crystal structure of the Lrp-like transcriptional regulator from the archaeon Pyrococcus furiosus.嗜热栖热菌中类Lrp转录调节因子的晶体结构
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A thermostable platform for transcriptional regulation: the DNA-binding properties of two Lrp homologs from the hyperthermophilic archaeon Methanococcus jannaschii.一种用于转录调控的热稳定平台:来自嗜热古菌詹氏甲烷球菌的两种Lrp同源物的DNA结合特性。
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Crystallization and secondary-structure determination of a protein of the Lrp/AsnC family from a hyperthermophilic archaeon.嗜热古菌Lrp/AsnC家族一种蛋白质的结晶及二级结构测定
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Transcription in archaea.古生菌中的转录。
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古菌的 feast/famine 调控蛋白:其组装形式在转录调控中的潜在作用

The archaeal feast/famine regulatory protein: potential roles of its assembly forms for regulating transcription.

作者信息

Koike Hideaki, Ishijima Sanae A, Clowney Lester, Suzuki Masashi

机构信息

National Institute of Advanced Industrial Science and Technology, Tsukuba Center 6-10, 1-1-1 Higashi, Tsukuba 305-8566, Japan.

出版信息

Proc Natl Acad Sci U S A. 2004 Mar 2;101(9):2840-5. doi: 10.1073/pnas.0400109101. Epub 2004 Feb 19.

DOI:10.1073/pnas.0400109101
PMID:14976242
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC365707/
Abstract

The classification feast/famine regulatory proteins (FFRPs) encompasses archaeal DNA-binding proteins with Escherichia coli transcription factors, the leucine-responsive regulatory protein and the asparagine synthase C gene product. In this paper, we describe two forms of the archaeal FFRP FL11 (pot0434017), both assembled from dimers. When crystallized, a helical cylinder is formed with six dimers per turn. In contrast, in solution, disks are formed, most likely consisting of four dimers each; an observation by cryoelectron microscopy. Whereas each dimer binds a 13-bp sequence, different forms will discriminate between promoters, based on the numbers of repeating 13-bp sequences, and types of linkers inserted between them, which are either of 7-8 or approximately 18 bp. The amino acid sequences of these FFRPs are designed to form the same type of 3D structures, and the transition between their assembly forms is regulated by interaction with small molecules. These considerations lead us to propose a possible mechanism for regulating a number of genes by varying assembly forms and by combining different FFRPs into these assemblies, responding to environmental changes.

摘要

分类的饥饱调节蛋白(FFRPs)包括具有大肠杆菌转录因子的古细菌DNA结合蛋白、亮氨酸响应调节蛋白和天冬酰胺合成酶C基因产物。在本文中,我们描述了古细菌FFRP FL11(pot0434017)的两种形式,二者均由二聚体组装而成。结晶时,会形成一个螺旋圆柱体,每圈有六个二聚体。相比之下,在溶液中会形成圆盘,很可能每个圆盘由四个二聚体组成;这是通过冷冻电子显微镜观察到的。虽然每个二聚体结合一个13bp的序列,但不同形式会根据重复13bp序列的数量以及插入其间的接头类型(7 - 8bp或约18bp)来区分启动子。这些FFRPs的氨基酸序列被设计成形成相同类型的三维结构,并且它们组装形式之间的转变受与小分子相互作用的调控。基于这些考虑,我们提出了一种可能的机制,即通过改变组装形式以及将不同的FFRPs组合到这些组装体中,来响应环境变化,从而调控多个基因。