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Chem Commun (Camb) ; 51(51): 10330-3, 2015 Jun 28.
Article in English | MEDLINE | ID: mdl-26027845

ABSTRACT

Bioorthogonal click ligations are extensively used for the introduction of functional groups in biological systems. Tetrazine ligations are attractive in that they are catalyst-free and display favorable kinetics. We describe the efficient remodeling of bacterial cell surfaces using unnatural d-amino acids derivatized with tetrazine ligation handles. The metabolic incorporation of these unnatural d-amino acids onto bacterial cell surfaces resulted in a site-selective installation of fluorophores.


Subject(s)
Fluorescent Dyes/chemistry , Heterocyclic Compounds, 1-Ring/chemistry , Peptidoglycan/chemistry , Amino Acids/chemistry , Click Chemistry , Diaminopimelic Acid/chemistry , Flow Cytometry , Norbornanes/chemistry , Peptidyl Transferases/metabolism , Staphylococcus aureus/chemistry , Stereoisomerism
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