The high-resolution structure of the extracellular domain of human CD69 using a novel polymer

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2009 Dec 1;65(Pt 12):1258-60. doi: 10.1107/S1744309109043152. Epub 2009 Nov 27.

Abstract

The structure of the extracellular domain of human CD69 has been determined by single-crystal X-ray diffraction. The structure refined to 1.37 A resolution provides further details of the overall structure and the asymmetric interface between the monomers in the native dimer. The protein was crystallized using di[poly(ethylene glycol)] adipate, which also served as a cryoprotectant. This is the first report of a crystal structure determined using crystals grown with this polymer.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / chemistry*
  • Antigens, Differentiation, T-Lymphocyte / chemistry*
  • Crystallography, X-Ray
  • Humans
  • Lectins, C-Type / chemistry*
  • Models, Molecular
  • Polymers / chemistry
  • Protein Conformation
  • Recombinant Proteins / chemistry

Substances

  • Antigens, CD
  • Antigens, Differentiation, T-Lymphocyte
  • CD69 antigen
  • Lectins, C-Type
  • Polymers
  • Recombinant Proteins

Associated data

  • PDB/3HUP
  • PDB/R3HUPSF