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Proceedings of the National Academy of Sciences of the United States of America logoLink to Proceedings of the National Academy of Sciences of the United States of America
. 1983 May;80(10):2922–2925. doi: 10.1073/pnas.80.10.2922

Some general principles in free energy transduction.

T L Hill
PMCID: PMC393945  PMID: 6222376

Abstract

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.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

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