Savageau M A, Freter R R
Biochemistry. 1979 Aug 7;18(16):3486-93. doi: 10.1021/bi00583a008.
The paradox of relatively error free function in biological systems composed of relatively error prone components has recently come under intensive investigation. In the case of tRNA aminoacylation, aminoacyl-tRNA synthetases were discovered to have a separate function that allows misacylated molecules to be hydrolyzed more rapidly than correctly acylated molecules. This additional function of the synthetases provides a proofreading or verification mechanism that is believed to improve significantly the overall accuracy of tRNA aminoacylation. In this paper we provide an explicit relationship between the accuracy achieved by proofreading and the energy cost. Experimental data available in the literature are examined in light of this relationship. The following are the principal conclusions from our study: (1) high-accuracy proofreading of tRNA aminoacylation has a high energy cost, as much as 100 times greater than indications from early experimental work; (2) the minimum net error derived in previous theoretical studies is never actually reached; (3) mechanisms in which misacylation and subsequent proofreading occur on the surface of the same synthetase molecule achieve a much higher accuracy than mechanisms in which these functions occur on the surface of different synthetase molecules.
由相对容易出错的组件构成的生物系统却具有相对无差错功能这一矛盾现象,近来受到了深入研究。就tRNA氨基酰化而言,人们发现氨基酰-tRNA合成酶具有一种独特功能,即能使错误酰化的分子比正确酰化的分子更快地被水解。合成酶的这一额外功能提供了一种校对或验证机制,据信该机制能显著提高tRNA氨基酰化的整体准确性。在本文中,我们给出了校对所实现的准确性与能量消耗之间的明确关系。依据这一关系对文献中的现有实验数据进行了审视。以下是我们研究的主要结论:(1)tRNA氨基酰化的高精度校对具有高昂的能量消耗,比早期实验工作所显示的高出多达100倍;(2)先前理论研究得出的最小净误差从未真正达到过;(3)错误酰化和后续校对在同一合成酶分子表面发生的机制,比这些功能在不同合成酶分子表面发生的机制具有更高的准确性。