| Literature DB >> 27629638 |
Po-Ssu Huang1,2,3, Scott E Boyken1,2,4, David Baker1,2,4.
Abstract
There are 20(200) possible amino-acid sequences for a 200-residue protein, of which the natural evolutionary process has sampled only an infinitesimal subset. De novo protein design explores the full sequence space, guided by the physical principles that underlie protein folding. Computational methodology has advanced to the point that a wide range of structures can be designed from scratch with atomic-level accuracy. Almost all protein engineering so far has involved the modification of naturally occurring proteins; it should now be possible to design new functional proteins from the ground up to tackle current challenges in biomedicine and nanotechnology.Entities:
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Year: 2016 PMID: 27629638 DOI: 10.1038/nature19946
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962