Rethinking the protein folding problem from a new perspective

被引:5
|
作者
Vila, Jorge A. [1 ]
机构
[1] Univ Nacl San Luis, IMASL, CONICET, Ejercito Andes 950, RA-5700 San Luis, Argentina
来源
EUROPEAN BIOPHYSICS JOURNAL WITH BIOPHYSICS LETTERS | 2023年 / 52卷 / 03期
关键词
AlphaFold; Analytic whole; Anfinsen; Force field; Leibniz and Kant; Protein folding; HELIX-COIL TRANSITION; FORCE-FIELD; STATISTICAL-MECHANICS; THEORETICAL APPROACH; PEPTIDES; EPISTASIS; RANGE; HOMOPOLYPEPTIDES; SIMULATIONS; EVOLUTION;
D O I
10.1007/s00249-023-01657-w
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
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.
引用
收藏
页码:189 / 193
页数:5
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