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- W3019381696 endingPage "2212" @default.
- W3019381696 startingPage "2199" @default.
- W3019381696 abstract "Nature provides a large number of functional proteins that evolved during billions of years of evolution. The diversity of natural proteins encompasses versatile functions and more than a thousand different folds, which, however, represents only a tiny fraction of all possible folds and polypeptide sequences. Recent advances in the rational design of proteins demonstrate that it is possible to design de novo protein folds unseen in nature. Novel protein topologies have been designed based on similar principles as natural proteins using advanced computational modelling or modular construction principles, such as oligomerization domains. Designed proteins exhibit several interesting features such as extreme stability, designability of 3D topologies and folding pathways. Moreover, designed protein assemblies can implement symmetry similar to the viral capsids, while, on the other hand, single‐chain pseudosymmetric designs can address each position independently. Recently, the design is expanding towards the introduction of new functions into designed proteins, and we may soon be able to design molecular machines." @default.
- W3019381696 created "2020-05-01" @default.
- W3019381696 creator A5029411682 @default.
- W3019381696 creator A5049606265 @default.
- W3019381696 creator A5055222513 @default.
- W3019381696 date "2020-05-09" @default.
- W3019381696 modified "2023-10-15" @default.
- W3019381696 title "Synthetic biology principles for the design of protein with novel structures and functions" @default.
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