Yu Tsyr-Yan, Schaefer Jacob
Department of Chemistry, Washington University, St. Louis, MO 63130, USA.
J Mol Biol. 2008 Oct 17;382(4):1031-42. doi: 10.1016/j.jmb.2008.07.077. Epub 2008 Aug 5.
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.
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。