dorsal/arxiv
View SchemaHierarchy of events in protein folding: beyond the Go model
| Authors | Ludovico Sutto, Guido Tiana, Ricardo A. Broglia |
|---|---|
| Categories | |
| ArXiv ID | q-bio/0601044 |
| URL | https://arxiv.org/abs/q-bio/0601044 |
Abstract
Simplified Go models, where only native contacts interact favorably, have proven useful to characterize some aspects of the folding of small proteins. The success of these models is limited by the fact that all residues interact in the same way, so that the folding features of a protein are determined only by the geometry of its native conformation. We present an extended version of a C-alpha based Go model where different residues interact with different energies. The model is used to calculate the thermodynamics of three small proteins (Protein G, SrcSH3 and CI2) and the effect of mutations on the wildtype sequence. The model allows to investigate some of the most controversial areas in protein folding such as its earliest stages, a subject which has lately received particular attention. The picture which emerges for the three proteins under study is that of a hierarchical process, where local elementary structures (LES) (not necessarily coincident with elements of secondary structure) are formed at the early stages of the folding and drive the protein, through the transition state and the postcritical folding nucleus (FN), resulting from the docking of the LES, to the native conformation.
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"abstract": "Simplified Go models, where only native contacts interact favorably, have\nproven useful to characterize some aspects of the folding of small proteins.\nThe success of these models is limited by the fact that all residues interact\nin the same way, so that the folding features of a protein are determined only\nby the geometry of its native conformation. We present an extended version of a\nC-alpha based Go model where different residues interact with different\nenergies. The model is used to calculate the thermodynamics of three small\nproteins (Protein G, SrcSH3 and CI2) and the effect of mutations on the\nwildtype sequence. The model allows to investigate some of the most\ncontroversial areas in protein folding such as its earliest stages, a subject\nwhich has lately received particular attention. The picture which emerges for\nthe three proteins under study is that of a hierarchical process, where local\nelementary structures (LES) (not necessarily coincident with elements of\nsecondary structure) are formed at the early stages of the folding and drive\nthe protein, through the transition state and the postcritical folding nucleus\n(FN), resulting from the docking of the LES, to the native conformation.",
"arxiv_id": "q-bio/0601044",
"authors": [
"Ludovico Sutto",
"Guido Tiana",
"Ricardo A. Broglia"
],
"categories": [
"q-bio.BM"
],
"title": "Hierarchy of events in protein folding: beyond the Go model",
"url": "https://arxiv.org/abs/q-bio/0601044"
},
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