Structural insights into the innate immune recognition specificities of L- and H-ficolins

EMBO J. 2007 Jan 24;26(2):623-33. doi: 10.1038/sj.emboj.7601500. Epub 2007 Jan 11.

Abstract

Innate immunity relies critically upon the ability of a few pattern recognition molecules to sense molecular markers on pathogens, but little is known about these interactions at the atomic level. Human L- and H-ficolins are soluble oligomeric defence proteins with lectin-like activity, assembled from collagen fibers prolonged by fibrinogen-like recognition domains. The X-ray structures of their trimeric recognition domains, alone and in complex with various ligands, have been solved to resolutions up to 1.95 and 1.7 A, respectively. Both domains have three-lobed structures with clefts separating the distal parts of the protomers. Ca(2+) ions are found at sites homologous to those described for tachylectin 5A (TL5A), an invertebrate lectin. Outer binding sites (S1) homologous to the GlcNAc-binding pocket of TL5A are present in the ficolins but show different structures and specificities. In L-ficolin, three additional binding sites (S2-S4) surround the cleft. Together, they define an unpredicted continuous recognition surface able to sense various acetylated and neutral carbohydrate markers in the context of extended polysaccharides such as 1,3-beta-D-glucan, as found on microbial or apoptotic surfaces.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Acetylation
  • Acetyltransferases / metabolism
  • Amino Acid Sequence
  • Binding Sites
  • Ficolins
  • Galactose / metabolism
  • Glycoproteins / chemistry*
  • Glycoproteins / genetics
  • Glycoproteins / metabolism
  • Humans
  • Immunity, Innate
  • Lectins / chemistry*
  • Lectins / genetics
  • Lectins / metabolism
  • Ligands
  • Models, Molecular
  • Molecular Sequence Data
  • Promoter Regions, Genetic
  • Protein Subunits / chemistry
  • Protein Subunits / metabolism
  • Sequence Homology, Amino Acid
  • Substrate Specificity
  • beta-Glucans / metabolism

Substances

  • FCN3 protein, human
  • Glycoproteins
  • Lectins
  • Ligands
  • Protein Subunits
  • beta-Glucans
  • beta-1,3-glucan
  • Acetyltransferases
  • Galactose