Phosphorylation energy hypothesis: open chemical systems and their biological functions

Annu Rev Phys Chem. 2007:58:113-42. doi: 10.1146/annurev.physchem.58.032806.104550.

Abstract

Biochemical systems and processes in living cells generally operate far from equilibrium. This review presents an overview of a statistical thermodynamic treatment for such systems, with examples from several key components in cellular signal transduction. Open-system nonequilibrium steady-state (NESS) models are introduced. The models account quantitatively for the energetics and thermodynamics in phosphorylation-dephosphorylation switches, GTPase timers, and specificity amplification through kinetic proofreading. The chemical energy derived from ATP and GTP hydrolysis establishes the NESS of a cell and makes the cell--a mesoscopic-biochemical reaction system that consists of a collection of thermally driven fluctuating macromolecules--a genetically programmed chemical machine.

Publication types

  • Review

MeSH terms

  • Kinetics
  • Models, Biological*
  • Models, Chemical
  • Phosphorylation
  • Proteins / chemistry
  • Proteins / metabolism
  • Thermodynamics

Substances

  • Proteins