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丝状噬菌体对称性理论

A theory of the symmetries of filamentous bacteriophages.

作者信息

Marzec C J, Day L A

机构信息

Department of Developmental and Structural Biology, Public Health Research Institute, New York, New York 10016.

出版信息

Biophys J. 1988 Mar;53(3):425-40. doi: 10.1016/S0006-3495(88)83119-9.

Abstract

A mathematical model is presented which explains the symmetries observed for the protein coats of filamentous bacterial viruses. Three viruses (Ff, IKe, and If1) all have five-start helices with rotation angles of 36 degrees and axial translations of 16 A (Type I symmetry), and three other viruses (Pf1, Xf, and Pf3) all have one-start helices with rotation angles of approximately equal to 67 degrees and translations of approximately 3 A (Type II symmetry). The coat protein subunits in each group diverge from each other in amino acid sequence, and Type II viruses differ dramatically in DNA structure. Regardless of the differences, both Type I and Type II symmetry can be understood as direct, natural consequences of the close-packing of alpha-helical protein subunits. In our treatment, an alpha-helical subunit is modeled as consisting of two interconnected, flexible tubular segments that follow helical paths around the DNA, one in an inner layer and the other in an outer layer. The mathematical model is a set of algebraic equations describing the disposition of the flexible segments. Solutions are described by newly introduced symmetry indices and other parameters. An exhaustive survey over the range of indices has produced a library of all structures that are geometrically feasible within our modeling scheme. Solutions which correspond in their rotation angles to Type I and Type II viruses occur over large ranges of the parameter space. A few solutions with other symmetries are also allowed, and viruses with these symmetries may exist in nature. One solution to the set of equations, obtained without any recourse to the x-ray data, yields a calculated x-ray diffraction pattern for Pf1 which compares reasonably with experimental patterns. The close-packing geometry we have used helps explain the near constant linear mass density of known filamentous phages. Helicoid, rigid cylinder, and maximum entropy structure models proposed by others for Pf1 are reconciled with the flexible tube models and with one another.

摘要

本文提出了一个数学模型,该模型解释了丝状细菌病毒蛋白质衣壳所观察到的对称性。三种病毒(Ff、IKe和If1)均具有五重螺旋,旋转角度为36度,轴向平移为16埃(I型对称性),另外三种病毒(Pf1、Xf和Pf3)均具有单重螺旋,旋转角度约为67度,平移约为3埃(II型对称性)。每组中的衣壳蛋白亚基在氨基酸序列上彼此不同,并且II型病毒在DNA结构上有显著差异。尽管存在这些差异,但I型和II型对称性都可以理解为α-螺旋蛋白亚基紧密堆积的直接自然结果。在我们的处理中,α-螺旋亚基被建模为由两个相互连接的柔性管状段组成,它们围绕DNA遵循螺旋路径,一个在内层,另一个在外层。该数学模型是一组描述柔性段排列的代数方程。通过新引入的对称性指数和其他参数来描述解。对指数范围进行的详尽调查产生了一个在我们的建模方案内几何上可行的所有结构的库。旋转角度与I型和II型病毒相对应的解出现在参数空间的很大范围内。也允许一些具有其他对称性的解,并且具有这些对称性的病毒可能在自然界中存在。在完全不参考X射线数据的情况下获得的一组方程的一个解,得出了Pf1的计算X射线衍射图,该图与实验图相当吻合。我们所使用的紧密堆积几何结构有助于解释已知丝状噬菌体近乎恒定的线性质量密度。其他人提出的针对Pf1的螺旋面、刚性圆柱体和最大熵结构模型与柔性管模型相互协调一致。

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A theory of the symmetries of filamentous bacteriophages.丝状噬菌体对称性理论
Biophys J. 1988 Mar;53(3):425-40. doi: 10.1016/S0006-3495(88)83119-9.

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本文引用的文献

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Dimensions of Xf virus from its rotational and translational diffusion coefficients.
Biochemistry. 1980 Apr 1;19(7):1373-6. doi: 10.1021/bi00548a016.
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The symmetries of filamentous phage particles.
J Mol Biol. 1981 Jan 25;145(3):611-7. doi: 10.1016/0022-2836(81)90549-0.
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Helix to helix packing in proteins.蛋白质中的螺旋-螺旋堆积
J Mol Biol. 1981 Jan 5;145(1):215-50. doi: 10.1016/0022-2836(81)90341-7.
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Structure of the filamentous bacteriophage, Pf3, by X-ray fiber diffraction.
J Mol Biol. 1982 Dec 25;162(4):877-81. doi: 10.1016/0022-2836(82)90552-6.
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