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• W2096536472 abstract "Protein design aims at designing new protein molecules of desired structure and functionality. One of the major obstacles to large-scale protein design are the extensive time and manpower requirements for experimental validation of designed sequences. Recent advances in protein structure prediction have provided potentials for an automated assessment of the designed sequences via folding simulations. We present a new protocol for protein design and validation. The sequence space is initially searched by Monte Carlo sampling guided by a public atomic potential, with candidate sequences selected by the clustering of sequence decoys. The designed sequences are then assessed by I-TASSER folding simulations, which generate full-length atomic structural models by the iterative assembly of threading fragments. The protocol is tested on 52 nonhomologous single-domain proteins, with an average sequence identity of 24% between the designed sequences and the native sequences. Despite this low sequence identity, three-dimensional models predicted for the first designed sequence have an RMSD of <2 Å to the target structure in 62% of cases. This percentage increases to 77% if we consider the three-dimensional models from the top 10 designed sequences. Such a striking consistency between the target structure and the structural prediction from nonhomologous sequences, despite the fact that the design and folding algorithms adopt completely different force fields, indicates that the design algorithm captures the features essential to the global fold of the target. On average, the designed sequences have a free energy that is 0.39 kcal/(mol residue) lower than in the native sequences, potentially affording a greater stability to synthesized target folds." @default.
• W2096536472 created "2016-06-24" @default.
• W2096536472 creator A5008108529 @default.
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• W2096536472 date "2011-04-01" @default.
• W2096536472 modified "2023-10-05" @default.
• W2096536472 title "Computational Protein Design and Large-Scale Assessment by I-TASSER Structure Assembly Simulations" @default.
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• W2096536472 doi "https://doi.org/10.1016/j.jmb.2011.02.017" @default.
• W2096536472 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/3070181" @default.
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