@article {1443,
	title = {Mycobacterial lipid logic.},
	journal = {Cell Host Microbe},
	volume = {15},
	year = {2014},
	month = {2014 Jan 15},
	pages = {1-2},
	abstract = {<p>During infection of the lung epithelium, Mycobacterium tuberculosis must infect and survive within macrophages long enough to be transported into deeper lung tissues. Cambier et~al. (2013) show that pathogenic mycobacteria use the coordinated action of two cell wall glycolipids to regulate macrophage recruitment to initial infection sites.</p>},
	keywords = {Animals, Female, Immune Evasion, Macrophages, Membrane Lipids, Mycobacterium},
	issn = {1934-6069},
	doi = {10.1016/j.chom.2013.12.005},
	author = {Siegrist, M Sloan and Bertozzi, Carolyn R}
}
@article {1446,
	title = {Probing the mycobacterial trehalome with bioorthogonal chemistry.},
	journal = {J Am Chem Soc},
	volume = {134},
	year = {2012},
	month = {2012 Oct 3},
	pages = {16123-6},
	abstract = {<p>Mycobacteria, including the pathogen Mycobacterium tuberculosis, use the non-mammalian disaccharide trehalose as a precursor for essential cell-wall glycolipids and other metabolites. Here we describe a strategy for exploiting trehalose metabolic pathways to label glycolipids in mycobacteria with azide-modified trehalose (TreAz) analogues. Subsequent bioorthogonal ligation with alkyne-functionalized probes enabled detection and visualization of cell-surface glycolipids. Characterization of the metabolic fates of four TreAz analogues revealed unique labeling routes that can be harnessed for pathway-targeted investigation of the mycobacterial trehalome.</p>},
	keywords = {Alkynes, Azides, Fluorescent Dyes, Glycolipids, Mycobacterium, Trehalose},
	issn = {1520-5126},
	doi = {10.1021/ja3062419},
	author = {Swarts, Benjamin M and Holsclaw, Cynthia M and Jewett, John C and Alber, Marina and Fox, Douglas M and Siegrist, M Sloan and Leary, Julie A and Kalscheuer, Rainer and Bertozzi, Carolyn R}
}
