Simons Center for Systems Biology, School of Natural Sciences, Institute for Advanced Study, Princeton, NJ 08540, USA.
Proc Natl Acad Sci U S A. 2012 Jul 24;109(30):12034-9. doi: 10.1073/pnas.1119911109. Epub 2012 Jul 11.
Proofreading mechanisms increase specificity in biochemical reactions by allowing for the dissociation of intermediate complexes. These mechanisms disrupt and reset the reaction to undo errors at the cost of increased time of reaction and free energy expenditure. Here, we draw an analogy between proofreading and microtubule growth which share some of the features described above. Our analogy relates the statistics of growth and shrinkage of microtubules in physical space to the cycling of intermediate complexes in the space of chemical states in proofreading mechanisms. Using this analogy, we find a new kinetic regime of proofreading in which an exponential speed-up of the process can be achieved at the cost of a somewhat larger error rate. This regime is analogous to the transition region between two known growth regimes of microtubules (bounded and unbounded) and is sharply defined in the limit of large proofreading networks. We find that this advantageous regime of speed-error tradeoff might be present in proofreading schemes studied earlier in the charging of tRNA by tRNA synthetases, in RecA filament assembly on ssDNA, and in protein synthesis by ribosomes.
校对机制通过允许中间复合物的解离来提高生化反应的特异性。这些机制破坏并重置反应,以消除错误,但代价是增加反应时间和自由能消耗。在这里,我们将校对与微管生长进行类比,它们具有上述一些共同特征。我们的类比将微管在物理空间中的生长和收缩的统计数据与校对机制中化学状态空间中中间复合物的循环联系起来。利用这种类比,我们发现了一种新的校对动力学状态,在这种状态下,过程可以以稍高的错误率为代价实现指数级加速。这种状态类似于微管的两种已知生长状态(有界和无界)之间的过渡区,并且在大的校对网络的极限下被明确地定义。我们发现,在 tRNA 合成酶对 tRNA 的充电、RecA 丝在 ssDNA 上的组装以及核糖体进行蛋白质合成等之前研究过的校对方案中,可能存在这种有利的速度-误差权衡的状态。