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Updated: Jun 16, 2026

Differential Scanning Calorimetry — A Method for Assessing the Thermal Stability and Conformation of Protein Antigen
Published on: March 4, 2017
Chemical and biochemical thermodynamics: from ATP hydrolysis to a general reassessment
Stefano Iotti1, Antonio Sabatini, Alberto Vacca
1Dipartimento di Medicina Interna dell'Invecchiamento e Malattie Nefrologiche, Università di Bologna, I-40138 Bologna, Italy. stefano.iotti@unibo.it
Abstract:
The Legendre-transformed Gibbs energy change for a biochemical reaction, Delta(r)G', is shown to be equal to the nontransformed Gibbs energy change, Delta(r)G, of any single reaction involving selected chemical species of the biochemical system. These two Gibbs energies of reaction have hitherto been thought to have different values. The equality of the quantities means that a substantial part of biochemical and chemical thermodynamics, previously treated separately, can be treated within a unified thermodynamic framework. An important consequence of the equality of Delta(r)G and Delta(r)G' is that the Gibbs energy change of many enzyme reactions can be quantified without specifying which chemical species is the active substrate of the enzyme. Another consequence is that the transformed standard Gibbs energy change of a reaction, Delta(r)G'(0), can be calculated by a simple analytical expression, rather than the complex computational methods of the past. The equality of the quantities is restricted to Gibbs energy changes and does not apply to enthalpy or entropy changes.
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