Format

Send to

Choose Destination
Mol Immunol. 2013 Dec;56(4):563-73. doi: 10.1016/j.molimm.2013.05.237. Epub 2013 Aug 1.

Review of phosphocholine substituents on bacterial pathogen glycans: synthesis, structures and interactions with host proteins.

Author information

1
Human Health Therapeutics, National Research Council of Canada, 100 Sussex Drive, Ottawa, Ontario, Canada K1A 0R6. Electronic address: martin.young@nrc-cnrc.gc.ca.

Abstract

Among the non-carbohydrate components of glycans, the addition of phosphocholine (ChoP) to the glycans of pathogens occurs more rarely than acetylation or methylation, but it has far more potent biological consequences. These arise from ChoP's multiple interactions with host proteins, which are important at all stages of the infection process. These stages include initial adherence to cells, encountering the host's innate immune system and then the adaptive immune system. Thus, in the initial stages of an infection, ChoP groups are an asset to the pathogen, but they can turn into a disadvantage subsequently. In this review, we have focussed on structural aspects of these phenomena. We describe the biosynthesis of the ChoP modification, the structures of the pathogen glycans known to carry ChoP groups and the host proteins that recognize ChoP.

KEYWORDS:

2-acetamido-4-amino-2,4,6-trideoxyhexose; C reactive protein; C-reactive protein; CRP; ChoP; Haemophilus influenzae; LTA; PAF; Phosphocholine; PnC; Streptococcus pneumoniae; TAA; ZPS; choline phosphate; lipotechoic acid; platelet-activating factor; pneumococcal C substance; zwitterionic polysaccharide

PMID:
23911414
DOI:
10.1016/j.molimm.2013.05.237
[Indexed for MEDLINE]
Free full text

Supplemental Content

Full text links

Icon for Elsevier Science
Loading ...
Support Center