Myths and verities in protein folding theories Part I: Anfinsen hypothesis and the search for the global minimum in the Gibbs energy landscape

Authors

  • Arieh Ben Naim The Hebrew University of Jerusalem Edmond J. Safra Campus Givat Ram, Jerusalem 91904

DOI:

https://doi.org/10.24297/jac.v3i2.932

Keywords:

Proteins, Second Law, Protein Folding, Native structure, Global minimum, Minimum Gibbs Energy, Anfinsen's Hypothesis

Abstract

Anfinsen’s thermodynamic hypothesis may be interpreted in two ways: One, that the native 3D structure of the protein, resides in the absolute minimum in the Gibbs energy landscape (GEL). The second, that the Gibbs energy functional, has a single (hence absolute) minimum at the equilibrium distribution of all accessible conformations of the protein. The second is equivalent to the Second Law of Thermodynamics. The first does not follow from the Second Law, and has no theoretical justification. Therefore, the search for an absolute minimum in the Gibbs energy landscape is not necessarily equivalent to a prediction of the native structure of the protein.

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Author Biography

Arieh Ben Naim, The Hebrew University of Jerusalem Edmond J. Safra Campus Givat Ram, Jerusalem 91904

Department of Physical Chemistry

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Published

2007-08-13

How to Cite

Naim, A. B. (2007). Myths and verities in protein folding theories Part I: Anfinsen hypothesis and the search for the global minimum in the Gibbs energy landscape. JOURNAL OF ADVANCES IN CHEMISTRY, 3(2), 197–204. https://doi.org/10.24297/jac.v3i2.932

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Articles