Kurland C G
Biophys J. 1978 Jun;22(3):373-92. doi: 10.1016/S0006-3495(78)85494-0.
It is not possible to select one competing substrate molecule over another one when the selection system is at equilibrium. Therefore, it is convenient to view all substrate selections as transport phenomena. The requirement for a displacement from equilibrium to effect a substrate selection can be met in different ways. One particularly convenient way is to drive a nonselected substrate, such as GTP in protein synthesis, far from equilibrium. This allows the flux of selected substrate to be relatively slow, but effectively irreversible. Accordingly, the conventional view that GTP hydrolysis drives protein synthesis is amended. It is suggested that the regeneration GTP from GDP is the driving force for protein synthesis. Several different selection mechanisms are described in the context fof systems driven by displacements from equilibrium of the nonselected substrate. These are then evaluated in light of recent experimental results. The data argue against the relevance of proofreading mechanisms for aminoacyl-tRNA selection by the messenger RNA-programmed ribosome. Similarly, recent data suggesting that the translation of messenger RNA is not dependent on the presence of elongation factors and guanine nucleotides are reevaluated.
当选择系统处于平衡状态时,不可能在一种竞争性底物分子和另一种之间进行选择。因此,将所有底物选择视为传输现象是很方便的。从平衡状态发生位移以实现底物选择的要求可以通过不同方式来满足。一种特别方便的方法是使未被选择的底物,例如蛋白质合成中的GTP,远离平衡状态。这使得被选择底物的通量相对较慢,但有效地不可逆。因此,传统观点认为GTP水解驱动蛋白质合成的观点被修正。有人提出,从GDP再生GTP是蛋白质合成的驱动力。在由未被选择底物的平衡位移驱动的系统背景下描述了几种不同的选择机制。然后根据最近的实验结果对这些机制进行评估。这些数据反驳了信使RNA编程核糖体对氨酰-tRNA选择的校对机制的相关性。同样,最近表明信使RNA翻译不依赖于延伸因子和鸟嘌呤核苷酸存在的数据也被重新评估。