Kremen A
J Theor Biol. 1984 Nov 7;111(1):47-60. doi: 10.1016/s0022-5193(84)80195-2.
Recognition processes with enhanced accuracy (as performed by structures like enzymes or ribosomes) are investigated using elementary ideas of statistical mechanics and related concepts of thermodynamics. The analysis starts from a formal definition of recognition and provides a correspondence with appropriate physical properties of the macromolecular logical elements. Transitions of the recognizing system between different modifications are a necessary feature of a more exacting recognition process. Rearrangement steps provide the process with higher accuracy by performing two physical operations: (1) rearranging the phase space of the system so that the "correct" states be better separated from the "wrong" states and the probability of occupation of the "correct" states be enhanced, (2) directing the process toward the more favourable modifications thus formed. Both operations are related to changes in the physical properties of the recognizing system. These changes can be expressed as differences of macromolecular Gibbs energy levels; if ligand binding or release participate in a step, directivity of the step depends also on the actual chemical potentials of the ligands in solution. The two operations just mentioned resemble two basic operations known to be necessary in electronic digital networks: directivity of control and signal standardization. An analysis of the entire reaction catalysed by a macromolecular logical element takes into account the requirements imposed by the logical functions as well as the need that the chemical potential of the product be not restricted to very low values. To satisfy these conditions, the reaction must be supported by a so-called non-specific reaction, usually implemented by the cleavage reaction of a nucleoside triphosphate.
利用统计力学的基本概念和热力学的相关概念,研究了具有更高准确性的识别过程(如由酶或核糖体等结构所执行的过程)。分析从识别的形式定义出发,并与大分子逻辑元件的适当物理性质建立对应关系。识别系统在不同修饰之间的转变是更严格的识别过程的一个必要特征。重排步骤通过执行两个物理操作,为该过程提供更高的准确性:(1)重新排列系统的相空间,以使“正确”状态与“错误”状态更好地分离,并提高占据“正确”状态的概率;(2)将过程导向由此形成的更有利的修饰。这两个操作都与识别系统物理性质的变化有关。这些变化可以表示为大分子吉布斯能级的差异;如果配体结合或释放参与一个步骤,该步骤的方向性还取决于溶液中配体的实际化学势。刚刚提到的这两个操作类似于电子数字网络中已知的两个基本操作:控制的方向性和信号标准化。对由大分子逻辑元件催化的整个反应的分析,考虑了逻辑功能所施加的要求以及产物化学势不限于非常低的值的必要性。为了满足这些条件,反应必须由所谓的非特异性反应来支持,通常由核苷三磷酸的裂解反应来实现。