Rethinking the protein folding problem from a new perspective

Eur Biophys J. 2023 Apr;52(3):189-193. doi: 10.1007/s00249-023-01657-w. Epub 2023 May 10.

Abstract

One of the main concerns of Anfinsen was to reveal the connection between the amino-acid sequence and their biologically active conformation. This search gave rise to two crucial questions in structural biology, namely, why the proteins fold and how a sequence encodes its folding. As to the why, he proposes a plausible answer, namely, the thermodynamic hypothesis. As to the how, this remains an unsolved challenge. Consequently, the protein folding problem is examined here from a new perspective, namely, as an 'analytic whole'. Conceiving the protein folding in this way enabled us to (i) examine in detail why the force-field-based approaches have failed, among other purposes, in their ability to predict the three-dimensional structure of a protein accurately; (ii) propose how to redefine them to prevent these shortcomings, and (iii) conjecture on the origin of the state-of-the-art numerical-methods success to predict the tridimensional structure of proteins accurately.

Keywords: AlphaFold; Analytic whole; Anfinsen; Force field; Leibniz and Kant; Protein folding.

MeSH terms

  • Amino Acid Sequence
  • Molecular Conformation
  • Protein Conformation
  • Protein Folding*
  • Proteins* / chemistry
  • Thermodynamics

Substances

  • Proteins