| Literature DB >> 30110557 |
Novalia Pishesha1,2, Jessica R Ingram3, Hidde L Ploegh1.
Abstract
Molecular biologists and chemists alike have long sought to modify proteins with substituents that cannot be installed by standard or even advanced genetic approaches. We here describe the use of transpeptidases to achieve these goals. Living systems encode a variety of transpeptidases and peptide ligases that allow for the enzyme-catalyzed formation of peptide bonds, and protein engineers have used directed evolution to enhance these enzymes for biological applications. We focus primarily on the transpeptidase sortase A, which has become popular over the past few years for its ability to perform a remarkably wide variety of protein modifications, both in vitro and in living cells.Keywords: cell surface labeling; nucleophile; protein engineering; sortase A; transpeptidases
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Year: 2018 PMID: 30110557 DOI: 10.1146/annurev-cellbio-100617-062527
Source DB: PubMed Journal: Annu Rev Cell Dev Biol ISSN: 1081-0706 Impact factor: 13.827