Crystallization and preliminary X-ray diffraction analysis of restriction endonuclease EcoRII

Acta Crystallogr D Biol Crystallogr. 1999 Sep;55(Pt 9):1604-5. doi: 10.1107/s090744499900863x.

Abstract

Crystals of the restriction endonuclease EcoRII have been obtained by the vapor-diffusion technique in the presence of ammonium sulfate or polyethylene glycol. The best crystals were grown with ammonium sulfate as a precipitant. Crystals with dimensions of up to 0.6 x 0. 6 x 0.6 mm have been observed. The crystals diffract to about 4.0 A resolution at a cryo-temperature of 100 K using a rotating-anode X-ray source and a Rigaku R-AXIS IV imaging-plate detector. The space group has been determined to be either I23 or I2(1)3, with unit-cell parameters a = b = c = 160.3 A, alpha = beta = gamma = 90 degrees. The crystal asymmetric unit contains two protein molecules, and self-rotation function analysis shows a pseudo-twofold symmetry relating the two monomers. Attempts to improve the resolution of crystal diffraction and to search for heavy-atom derivatives are under way.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Ammonium Sulfate
  • Chemical Precipitation
  • Crystallization
  • Deoxyribonucleases, Type II Site-Specific / chemistry*
  • Diffusion
  • Molecular Weight
  • Polyethylene Glycols
  • Volatilization
  • X-Ray Diffraction

Substances

  • Polyethylene Glycols
  • CCWGG-specific type II deoxyribonucleases
  • Deoxyribonucleases, Type II Site-Specific
  • Ammonium Sulfate