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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
. 1977 Dec;74(12):5227–5230. doi: 10.1073/pnas.74.12.5227

"Viral" expansion of enzyme flux and use of quasi-chemical approximation for two-state enzymes with enzyme-enzyme interactions.

T L Hill
PMCID: PMC431658  PMID: 271948

Abstract

Two examples of enzyme systems with interactions, at steady state, are treated here. In both cases, the enzyme cycle has two states and quasi-equilibrium in spatial distributions obtains at steady state (because f alpha + f beta = 1). The first example is a dilute solution of enzyme molecules in a solvent. The flux (turnover) per molecule is expanded in powers of the enzyme concentration (a "viral" expansion). Aggregation of the enzyme molecules in solution is considered as a special case. In the second example, we treat an arbitrary lattice of enzyme molecules, with nearest-neighbor interactions, using the well-known quasi-chemical approximation. The flux per molecule is obtained. Critical behavior and hysteresis are illustrated.

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Selected References

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

  1. Hill T. L. Further study of the effect of enzyme-enzyme interactions on steady-state enzyme kinetics. Proc Natl Acad Sci U S A. 1977 Oct;74(10):4111–4115. doi: 10.1073/pnas.74.10.4111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Hill T. L. Theoretical study of the effect of enzyme-enzyme interactions on steady-state enzyme kinetics. Proc Natl Acad Sci U S A. 1977 Sep;74(9):3632–3636. doi: 10.1073/pnas.74.9.3632. [DOI] [PMC free article] [PubMed] [Google Scholar]

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