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REDOR NMR characterization of DNA packaging in bacteriophage T4.噬菌体T4中DNA包装的REDOR NMR表征
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2
Structure, assembly, and DNA packaging of the bacteriophage T4 head.噬菌体 T4 头部的结构、组装和 DNA 包装。
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Structure-function analysis of the DNA translocating portal of the bacteriophage T4 packaging machine.噬菌体T4包装机器DNA转运门户的结构-功能分析
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Controlling the Revolving and Rotating Motion Direction of Asymmetric Hexameric Nanomotor by Arginine Finger and Channel Chirality.通过精氨酸手指和通道手性控制不对称六聚体纳米马达的旋转和转动运动方向。
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Single phage T4 DNA packaging motors exhibit large force generation, high velocity, and dynamic variability.单个噬菌体T4 DNA包装马达表现出强大的力产生、高速度和动态变异性。
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Measurements of single DNA molecule packaging dynamics in bacteriophage lambda reveal high forces, high motor processivity, and capsid transformations.对噬菌体λ中单个DNA分子包装动力学的测量揭示了高作用力、高马达持续性和衣壳转变。
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噬菌体T4中DNA包装的REDOR NMR表征

REDOR NMR characterization of DNA packaging in bacteriophage T4.

作者信息

Yu Tsyr-Yan, Schaefer Jacob

机构信息

Department of Chemistry, Washington University, St. Louis, MO 63130, USA.

出版信息

J Mol Biol. 2008 Oct 17;382(4):1031-42. doi: 10.1016/j.jmb.2008.07.077. Epub 2008 Aug 5.

DOI:10.1016/j.jmb.2008.07.077
PMID:18703073
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2633174/
Abstract

Bacteriophage T4 is a large-tailed Escherichia coli virus whose capsid is 120x86 nm. ATP-driven DNA packaging of the T4 capsid results in the loading of a 171-kb genome in less than 5 min during viral infection. We have isolated 50-mg quantities of uniform (15)N- and [epsilon-(15)N]lysine-labeled bacteriophage T4. We have also introduced (15)NH(4)(+) into filled, unlabeled capsids from synthetic medium by exchange. We have examined lyo- and cryoprotected lyophilized T4 using (15)N{(31)P} and (31)P{(15)N} rotational-echo double resonance. The results of these experiments have shown that (i) packaged DNA is in an unperturbed duplex B-form conformation; (ii) the DNA phosphate negative charge is balanced by lysyl amines (3.2%), polyamines (5.8%), and monovalent cations (40%); and (iii) 11% of lysyl amines, 40% of -NH(2) groups of polyamines, and 80% of monovalent cations within the lyophilized T4 capsid are involved in the DNA charge balance. The NMR evidence suggests that DNA enters the T4 capsid in a charge-unbalanced state. We propose that electrostatic interactions may provide free energy to supplement the nanomotor-driven T4 DNA packaging.

摘要

噬菌体T4是一种具有大尾巴的大肠杆菌病毒,其衣壳大小为120×86纳米。在病毒感染期间,T4衣壳由ATP驱动的DNA包装过程能在不到5分钟的时间内装入一个171千碱基对的基因组。我们已分离出50毫克均匀的(15)N和[ε-(15)N]赖氨酸标记的噬菌体T4。我们还通过交换将(15)NH4+引入到来自合成培养基的已填充、未标记的衣壳中。我们使用(15)N{(31)P}和(31)P{(15)N}旋转回波双共振研究了冻干和冷冻保护的冻干T4。这些实验结果表明:(i)包装的DNA处于未受干扰的双链B型构象;(ii)DNA磷酸基团的负电荷由赖氨胺(3.2%)、多胺(5.8%)和单价阳离子(40%)平衡;(iii)冻干的T4衣壳内11%的赖氨胺、40%的多胺-NH2基团和80%的单价阳离子参与DNA电荷平衡。核磁共振证据表明DNA以电荷不平衡状态进入T4衣壳。我们提出静电相互作用可能提供自由能以补充纳米马达驱动的T4 DNA包装。