Hill T L
Proc Natl Acad Sci U S A. 1983 May;80(10):2922-5. doi: 10.1073/pnas.80.10.2922.
Chemical potentials or standard chemical potentials of bound ligands cannot be used to follow the step-by-step transfer of free energy from one ligand to another in a free energy transducing cycle. The basic difficulty is that, in most states of the cycle, separate ligand free energies are not even defined because, when ligands are bound on the enzyme, the interaction free energy of the complex cannot simply be assigned to ligands nor in general even be divided between two ligands if both are bound. This is a mutual, indivisible free energy among enzyme and ligands. Separate ligand free energies are well defined only at the complete cycle level, where the enzyme drops out of consideration (returns to its original state). Other types of free energy are also considered in order to discuss recent work of Tanford. In principle, the kinetics and mechanism can be followed in molecular or atomic detail through the steps of a transduction cycle, but the transfer of free energy from one ligand to another cannot be so followed.
结合配体的化学势或标准化学势不能用于跟踪自由能在自由能转导循环中从一个配体到另一个配体的逐步转移。基本困难在于,在循环的大多数状态下,单独的配体自由能甚至没有定义,因为当配体与酶结合时,复合物的相互作用自由能不能简单地归属于配体,而且如果两个配体都结合,通常甚至不能在它们之间进行分配。这是酶和配体之间相互的、不可分割的自由能。单独的配体自由能仅在完整循环水平上才有明确的定义,此时酶不再被考虑(恢复到其原始状态)。为了讨论坦福德最近的工作,还考虑了其他类型的自由能。原则上,可以在分子或原子细节上跟踪转导循环步骤中的动力学和机制,但自由能从一个配体到另一个配体的转移则无法这样跟踪。