| Literature DB >> 34761448 |
Abstract
To expand protein's covalent bonding ability, latent bioreactive unnatural amino acids have been designed and genetically encoded into proteins, which react with specific natural amino acid residues through proximity-enabled bioreactivity. The resultant new covalent bonds can be selectively created within and between proteins in vitro, in cells, and in vivo. Offering diverse properties previously unattainable, these covalent linkages have been harnessed to enhance protein properties, to modulate protein function, to probe ligand-receptor binding, to identify elusive protein interactions, and to develop covalent protein drugs. Selective introduction of covalent bonds into proteins is affording novel avenues for biological studies, synthetic biology, and biotherapeutics.Entities:
Keywords: covalent drug; genetic code expansion; latent bioreactive unnatural amino acid; protein therapeutics; protein-protein interaction; proximity-enabled bioreactivity
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Year: 2021 PMID: 34761448 PMCID: PMC8819847 DOI: 10.1002/pro.4228
Source DB: PubMed Journal: Protein Sci ISSN: 0961-8368 Impact factor: 6.725