| Literature DB >> 26958882 |
Dominique T Capraro1, Patricia A Jennings2.
Abstract
Entanglement and knots occur across all aspects of the physical world. Despite the common belief that knots are too complicated for incorporation into proteins, knots have been identified in the native fold of a growing number of proteins. The discovery of proteins with this unique backbone characteristic has challenged the preconceptions about the complexity of biological structures, as well as current folding theories. Given the intricacies of the knotted geometry, the interplay between a protein's fold, structure, and function is of particular interest. Interestingly, for most of these proteins, the knotted region appears critical both in folding and function, although full understanding of these contributions is still incomplete. Here, we experimentally reveal the impact of the knot on the landscape, the origin of the bistable nature of the knotted protein, and broaden the view of knot formation as uniquely decoupled from folding.Mesh:
Substances:
Year: 2016 PMID: 26958882 PMCID: PMC4788744 DOI: 10.1016/j.bpj.2016.01.017
Source DB: PubMed Journal: Biophys J ISSN: 0006-3495 Impact factor: 4.033