Crystallization and preliminary crystallographic studies on the large extracellular domain of human CD81, a tetraspanin receptor for hepatitis C virus

Acta Crystallogr D Biol Crystallogr. 2001 Jan;57(Pt 1):156-8. doi: 10.1107/s0907444900015468.

Abstract

The large extracellular domain of CD81, a member of the tetraspanin family and a receptor protein for hepatitis C virus envelope E2 glycoprotein, has been expressed, purified and subsequently crystallized using the sitting-drop vapour-diffusion technique. Native diffraction data to 1.6 A resolution were obtained at the ID14 beamline of the European Synchrotron Radiation Facility from a flash-frozen crystal at 100 K. The crystals belong to space group P2(1), with unit-cell parameters a = 31.5, b = 77.2, c = 38.5 A, beta = 107.4 degrees, and are likely to contain two extracellular domains (2 x 99 residues) per asymmetric unit.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Antigens, CD / chemistry*
  • Antigens, CD / physiology
  • Base Sequence
  • Crystallization
  • Crystallography, X-Ray
  • DNA Primers
  • Hepacivirus / physiology*
  • Humans
  • Membrane Proteins*
  • Receptors, Virus / chemistry*
  • Receptors, Virus / physiology
  • Recombinant Proteins / chemistry
  • Tetraspanin 28

Substances

  • Antigens, CD
  • CD81 protein, human
  • DNA Primers
  • Membrane Proteins
  • Receptors, Virus
  • Recombinant Proteins
  • Tetraspanin 28