Yan J, Magnasco M O, Marko J F
Department of Physics, The University of Illinois at Chicago, 60607, USA.
Nature. 1999 Oct 28;401(6756):932-5. doi: 10.1038/44872.
Cells must remove all entanglements between their replicated chromosomal DNAs to segregate them during cell division. Entanglement removal is done by ATP-driven enzymes that pass DNA strands through one another, called type II topoisomerases. In vitro, some type II topoisomerases can reduce entanglements much more than expected, given the assumption that they pass DNA segments through one another in a random way. These type II topoisomerases (of less than 10 nm in diameter) thus use ATP hydrolysis to sense and remove entanglements spread along flexible DNA strands of up to 3,000 nm long. Here we propose a mechanism for this, based on the higher rate of collisions along entangled DNA strands, relative to collision rates on disentangled DNA strands. We show theoretically that if a type II topoisomerase requires an initial 'activating' collision before a second strand-passing collision, the probability of entanglement may be reduced to experimentally observed levels. This proposed two-collision reaction is similar to 'kinetic proofreading' models of molecular recognition.
细胞必须消除其复制的染色体DNA之间的所有缠结,以便在细胞分裂期间将它们分离。缠结的消除是由ATP驱动的酶完成的,这些酶使DNA链相互穿过,称为II型拓扑异构酶。在体外,一些II型拓扑异构酶减少缠结的能力比预期的要强得多,前提是假设它们以随机方式使DNA片段相互穿过。因此,这些直径小于10纳米的II型拓扑异构酶利用ATP水解来感知并消除沿着长达3000纳米的柔性DNA链分布的缠结。在此,我们基于缠结的DNA链上的碰撞速率相对于解缠结的DNA链上的碰撞速率更高,提出了一种对此的机制。我们从理论上表明,如果II型拓扑异构酶在第二次链穿过碰撞之前需要一次初始的“激活”碰撞,那么缠结的概率可能会降低到实验观察到的水平。这种提出的双碰撞反应类似于分子识别的“动力学校对”模型。