Author(s) -
M. Sloan Siegrist,
Sarah A. Whiteside,
John C. Jewett,
Arjun K. Aditham,
Felipe Cava,
Carolyn R. Bertozzi
Publication year - 2012
Publication title -
acs chemical biology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.899
H-Index - 111
eISSN - 1554-8937
pISSN - 1554-8929
DOI - 10.1021/cb3004995
Subject(s) - bioorthogonal chemistry , peptidoglycan , click chemistry , intracellular , biochemistry , chemistry , pathogen , bacterial cell structure , alanine , listeria monocytogenes , cell wall , bacteria , in vivo , in vitro , amino acid , biology , microbiology and biotechnology , combinatorial chemistry , genetics
Peptidoglycan (PG) is an essential component of the bacterial cell wall. Although experiments with organisms in vitro have yielded a wealth of information on PG synthesis and maturation, it is unclear how these studies translate to bacteria replicating within host cells. We report a chemical approach for probing PG in vivo via metabolic labeling and bioorthogonal chemistry. A wide variety of bacterial species incorporated azide and alkyne-functionalized d-alanine into their cell walls, which we visualized by covalent reaction with click chemistry probes. The d-alanine analogues were specifically incorporated into nascent PG of the intracellular pathogen Listeria monocytogenes both in vitro and during macrophage infection. Metabolic incorporation of d-alanine derivatives and click chemistry detection constitute a facile, modular platform that facilitates unprecedented spatial and temporal resolution of PG dynamics in vivo.
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