用光镊操作单个DNA分子研究了噬菌体φ29 DNA包装对离子条件的依赖性

Derek N. Fuller, J. P. Rickgauer, S. Grimes, P. Jardine, D. Anderson, Douglas E. Smith
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引用次数: 0

摘要

φ29噬菌体入口马达能够将φ29 (19.3 Kbp)基因组高密度包装到预成型的衣壳中。包装过程必须克服由于将DNA的高负电荷限制在小体积内而产生的力,以及由于DNA在小于一个持久长度的长度尺度上弯曲而产生的力。这两种能量的考虑都可以通过DNA包装发生的缓冲液的离子性质来调节。为了测量DNA电荷屏蔽对包装过程的影响,我们用光学镊子研究了不同离子条件下DNA包装的动力学。我们观察了一价、二价和三价阳离子对运动功能的影响及其对外力的依赖,我们观察了名义力下DNA包装率作为衣壳填充的函数。具体来说,我们在包装过程中改变了浸泡在噬菌体溶液中的Na+、Mg+2和钴的浓度,看看这些阳离子有什么影响,如果有的话。从这些测量中,我们提出了一个推断的内力,作为在各种离子环境中噬菌体衣壳填充百分比的函数。初步分析表明,离子环境可以调节内部压力,随着高价阳离子的存在,更好地屏蔽包装DNA,从而降低内部压力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Dependence of bacteriophage φ29 DNA packaging on ionic conditions studied by optical tweezers manipulation of single DNA molecules
The bacteriophage φ29 portal motor is capable of packaging the φ29, 19.3 Kbp, genome to high density into its preformed capsid. The packaging process must overcome the forces due to confining the highly negative charge of the DNA to a small volume, as well as the forces due to bending the DNA on length scales smaller than one persistence length. Both of these energetic considerations can be modulated by the ionic nature of the buffer DNA packaging occurs in. To measure the effects of DNA charge shielding on the packaging process, we studied the dynamics of DNA packaging by optical tweezers in a variety of different ionic conditions. We looked at the effects monovalent, divalent, and trivalent cations have on the motor function and its dependence on external force and, we observed the rate of DNA packaging at nominal force as a function of capsid filling. Specifically, we varied the concentrations of Na+, Mg+2, and cobalt hexamine in the solution bathing the bacteriophage during packaging to see what effects, if any, these cations have. From these measurements, we present an inferred internal force as a function of percent filling of the bacteriophage capsid in a variety of ionic environments. Preliminary analysis suggests the ionic environment can modulate internal pressure, with the presence of higher valence cations better shielding the packaged DNA resulting in lower internal pressures.
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