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PMID: 15644310 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Crystal structure of CD14 and its implications for lipopolysaccharide signaling.

The Journal of biological chemistry ·Vol. 280 ·No. 12 ·2005-03-25 ·Pages 11347-51

Kim JI, Lee CJ, Jin MS, Lee CH, Paik SG, Lee H, Lee JO

Abstract

Lipopolysaccharide, the endotoxin of Gram-negative bacteria, induces extensive immune responses that can lead to fatal septic shock syndrome. The core receptors recognizing lipopolysaccharide are CD14, TLR4, and MD-2. CD14 binds to lipopolysaccharide and presents it to the TLR4/MD-2 complex, which initiates intracellular signaling. In addition to lipopolysaccharide, CD14 is capable of recognizing a few other microbial and cellular products. Here, we present the first crystal structure of CD14 to 2.5 angstroms resolution. A large hydrophobic pocket was found on the NH2-terminal side of the horseshoe-like structure. Previously identified regions involved in lipopolysaccharide binding map to the rim and bottom of the pocket indicating that the pocket is the main component of the lipopolysaccharide-binding site. Mutations that interfere with lipopolysaccharide signaling but not with lipopolysaccharide binding are also clustered in a separate area near the pocket. Ligand diversity of CD14 could be explained by the generous size of the pocket, the considerable flexibility of the rim of the pocket, and the multiplicity of grooves available for ligand binding.

MeSH Terms
Amino Acid Sequence Animals Antigens, Ly/physiology Hydrophobic and Hydrophilic Interactions Lipopolysaccharide Receptors/chemistry,metabolism Lipopolysaccharides/metabolism Lymphocyte Antigen 96 Mice Molecular Sequence Data Protein Structure, Secondary Receptors, Cell Surface/physiology Signal Transduction Toll-Like Receptor 4
Chemicals
Antigens, Ly Lipopolysaccharide Receptors Lipopolysaccharides Ly96 protein, mouse Lymphocyte Antigen 96 Receptors, Cell Surface Tlr4 protein, mouse Toll-Like Receptor 4
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kim Jung-In
Department of Chemistry, Korea Advanced Institute of Science and Technology, Daejeon 305-701, Korea.
Lee Chang Jun
Jin Mi Sun
Lee Cherl-Ho
Paik Sang-Gi
Lee Hayyoung
Lee Jie-Oh
Article Info
Journal
The Journal of biological chemistry
Abbr.
J Biol Chem
ISSN
0021-9258
Published
2005-03-25
Epub
2005-00-10
Pages
11347-51
Language
English
Region
United States
NLM ID
2985121R
Subset
IM
Databases
PDB
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