Hess B, Mikhailov A
Max-Planck-Institut für medizinische Forschung, Heidelberg, Germany.
J Theor Biol. 1995 Sep 7;176(1):181-4. doi: 10.1006/jtbi.1995.0187.
Biochemical subsystems of a living cell may operate with only a few thousand enzyme molecules and their response can be triggered by the entrance of individual molecules of a certain species. This mode of operation is not described by classical chemical kinetics, which deals with large numbers of reacting molecules. Theoretical estimates for the characteristic times of enzymic reactions in small cells and cellular compartments show that any two macromolecules within a micrometer-size volume meet each other each second and that the transit time, required for a mediator molecule to meet a target enzyme, is comparable to the duration of a catalytic round for a single enzyme molecule. When these conditions are satisfied, an enzymic subsystem represents a coherent molecular network with persistent strong temporal correlations between the catalytic events of individual enzyme molecules.
活细胞的生化子系统可能仅靠几千个酶分子就能运行,其反应可由特定种类单个分子的进入引发。这种运行模式并非传统化学动力学所能描述,传统化学动力学处理的是大量反应分子。对小细胞和细胞区室中酶促反应特征时间的理论估计表明,在一微米大小的体积内,任意两个大分子每秒都会相遇,且介导分子与靶酶相遇所需的转运时间与单个酶分子一轮催化所需的持续时间相当。当这些条件满足时,酶子系统就代表了一个连贯的分子网络,单个酶分子的催化事件之间存在持续的强时间相关性。