Schein Stan
California NanoSystems Institute, UCLA, Los Angeles, CA 90095-7151, USA.
J Mol Biol. 2009 Mar 27;387(2):363-75. doi: 10.1016/j.jmb.2009.01.044. Epub 2009 Jan 29.
Fullerene cages have n trivalent vertices, 12 pentagonal faces, and (n-20)/2 hexagonal faces. The smallest cage in which all of the pentagons are surrounded by hexagons and thus isolated from each other has 60 vertices and is shaped like a soccer ball. The protein clathrin self-assembles into fullerene cages of a variety of sizes and shapes, including smaller ones with adjacent pentagons as well as larger ones, but the variety is limited. To explain the range of clathrin architecture and how these fullerene cages self-assemble, we proposed a hypothesis, the "head-to-tail exclusion rule" (the "Rule"). Of the 5769 small clathrin cage isomers with n< or =60 vertices and adjacent pentagons, the Rule permits just 15, three identified in 1976 and 12 others. A "weak version" of the Rule permits another 99. Based on cryo-electron tomography, Cheng et al. reported six raw clathrin fullerene cages. One was among the three identified in 1976. Here, (1) we identify the remaining five. (2) Four are new and are among the 12 others permitted by the Rule. (3) One, also new, is among the 99 weak version cages. (4) Of particular note, none of the remaining 5565 excluded cages has been identified. These findings provide powerful experimental confirmation of the Rule and the principle on which it is based. (5) Surprisingly, the newly identified clathrin cages are among the least symmetric of those permitted. (6) By devising a method for counting assembly paths, (7) we show that asymmetric cages can be assembled by larger numbers of paths, thus providing a kinetic explanation for the prevalence of asymmetric cages. (8) Finally, we show that operation during cage growth of the Rule greatly increases the likelihood of producing a closed fullerene cage, specifically one of those permitted, but efficient assembly still appears to require internal remodeling.
富勒烯笼有(n)个三价顶点、(12)个五边形面和((n - 20)/2)个六边形面。最小的笼中所有五边形都被六边形包围且彼此隔离,它有(60)个顶点,形状像足球。蛋白质网格蛋白能自组装成各种大小和形状的富勒烯笼,包括有相邻五边形的较小笼子以及较大的笼子,但种类有限。为了解释网格蛋白结构的范围以及这些富勒烯笼如何自组装,我们提出了一个假设,即“头对尾排斥规则”(“规则”)。在(n\leq60)个顶点且有相邻五边形的(5769)种小网格蛋白笼异构体中,该规则只允许(15)种,其中三种在1976年已被识别,另外还有(12)种。该规则的“弱版本”允许另外(99)种。基于冷冻电子断层扫描,程等人报告了六个原始的网格蛋白富勒烯笼。其中一个是1976年识别出的三种之一。在此,(1)我们识别出其余五个。(2)四个是新的,属于该规则允许的另外(12)种。(3)一个也是新的,属于(99)个弱版本笼子。(4)特别值得注意的是,其余(5565)种被排除的笼子都未被识别。这些发现有力地实验证实了该规则及其所基于的原理。(5)令人惊讶的是,新识别出的网格蛋白笼是所允许的笼子中对称性最低的。(6)通过设计一种计算组装路径的方法,(7)我们表明不对称笼子可以通过更多数量的路径组装,从而为不对称笼子的普遍存在提供了动力学解释。(8)最后,我们表明该规则在笼生长过程中的作用极大地增加了产生封闭富勒烯笼的可能性,特别是那些所允许的笼子,但高效组装似乎仍需要内部重塑。