| Literature DB >> 30231608 |
Thibault J Harmand1, Djenet Bousbaine1,2, Alix Chan3, Xiaohong Zhang4, David R Liu3, James P Tam4, Hidde L Ploegh1.
Abstract
Site-specific chemical modification of proteins can assist in the study of their function. Furthermore, these methods are essential to develop biologicals for diagnostic and therapeutic use. Standard protein engineering protocols and recombinant expression enable the production of proteins with short peptide tags recognized by enzymes capable of site-specific modification. We report here the application of two enzymes of orthogonal specificity, sortase A and butelase 1, to prepare non-natural C-to-C fusion proteins. Using these enzymes, we further demonstrate site-selective installation of different chemical moieties at two sites in a full-size antibody molecule.Entities:
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Year: 2018 PMID: 30231608 PMCID: PMC6429940 DOI: 10.1021/acs.bioconjchem.8b00563
Source DB: PubMed Journal: Bioconjug Chem ISSN: 1043-1802 Impact factor: 4.774