Journal of the American Chemical Society · 2021 · 10 citations · 51 references
Life SciencesBiochemistryMolecular BiologyProtein EngineeringProtein FoldingStructural BiologyFolding KineticsFolding ThermodynamicsProtein DesignProtein DynamicsProtein RefoldingProtein StructureMolecular Dynamics Of FoldingPeptide FoldingProtein Folding EnergeticsProtein Folding SimulationsRational DesignSingle-molecule KineticsStopped-flow SpectroscopyUbiquitin System
, with significant consequences for the living organism and the pharmaceutical industry, respectively. Here we propose a design principle for small-peptide-based protein-specific folding modifiers. The principle is based on constructing a "xenonucleus", which is a prefolded peptide that mimics the folding nucleus of a protein. Using stopped-flow kinetics, NMR spectroscopy, Förster resonance energy transfer, single-molecule force measurements, and molecular dynamics simulations, we demonstrate that a xenonucleus can make the refolding of ubiquitin faster by 33 ± 5%, while variants of the same peptide have little or no effect. Our approach provides a novel method for constructing specific, genetically encodable folding catalysts for suitable proteins that have a well-defined contiguous folding nucleus.
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Principles that Govern the Folding of Protein Chains
Christian B. Anfinsen · Science · 1973 · 7.1K citations
John F. Marko, Eric D. Siggia · Macromolecules · 1995 · 2.3K citations
How Fast-Folding Proteins Fold
Kresten Lindorff‐Larsen, Stefano Piana, Ron O. Dror et al. · Science · 2011 · 2K citations