| Literature DB >> 16920483 |
Alberto Visintin1, Dimitar B Iliev, Brian G Monks, Kristen A Halmen, Douglas T Golenbock.
Abstract
Toll-like receptors (TLRs) are a small family of type-I glycoproteins that bind to and are activated by conserved non-self molecular signatures carried by microorganisms. Toll-like receptor 4 is triggered by most lipopolysaccharides (LPS). LPS is a complex amphipathic saccharolipidic glycan derived from Gram-negative bacteria. Unique among TLRs, TLR4 activity and interaction with its natural ligand(s) strictly depends on the presence of the extracellular adaptor MD-2. MD-2 is a small secreted glycoprotein that binds with cytokine-like affinities to both the hydrophobic portion of LPS and to the extracellular domain of TLR4. The interaction between MD-2 and LPS induces a triggering event on TLR4, which involves the molecular rearrangement of the receptor complex and its homotypic aggregation. In silico analysis suggests that MD-2 and MD-1 are paralogs derived from a common predecessor at the level of early vertebrates. In this review, we summarize the current state of knowledge concerning MD-2.Entities:
Mesh:
Substances:
Year: 2006 PMID: 16920483 DOI: 10.1016/j.imbio.2006.05.010
Source DB: PubMed Journal: Immunobiology ISSN: 0171-2985 Impact factor: 3.144