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Título: | Do theoretical physicists care about the protein-folding problem? |
Autor: | Alonso, José Luis CSIC ORCID; Chass, Gregory; Csizmadia, Imre; Echenique, Pablo CSIC ORCID; Tarancón, Alfonso | Palabras clave: | protein folding simple models |
Fecha de publicación: | 2004 | Editor: | Aula Documental de Investigación | Citación: | Meeting on Fundamental Physics ‘Alberto Galindo’ | Resumen: | The prediction of the biologically active native conformation of a protein is one of the fundamental challenges of structural biology. This problem remains yet unsolved mainly due to three factors: the partial knowledge of the effective free energy function that governs the folding process, the enormous size of the conformational space of a protein and, finally, the relatively small differences of energy between conformations, in particular, between the native one and the ones that make up the unfolded state. Herein, we recall the importance of taking into account, in a detailed manner, the many interactions involved in the protein-folding problem (such as steric volume exclusion, Ramachandran forces, hydrogen bonds, weakly polar interactions, coulombic energy or hydrophobic attraction) and we propose a strategy to effectively construct a free energy function that, including the effects of the solvent, could be numerically tractable. We also describe the situation in which the native conformation has different covalent constraints than the unfolded state (such as disulfide linkages), and then the exact native structure can not be reached using the original free energy function. Finally, we discuss about the limits and the lacks from which suffer the simple models that we, physicists, love so much. | URI: | http://hdl.handle.net/10261/78169 |
Aparece en las colecciones: | (IQF) Libros y partes de libros |
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2004_GalindoBOOKFolding.pdf | 599,92 kB | Adobe PDF | Visualizar/Abrir |
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