Purification, crystallization and preliminary crystallographic analysis of Est25: a ketoprofen-specific hormone-sensitive lipase

Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Jul 1;63(Pt 7):579-81. doi: 10.1107/S1744309107026152. Epub 2007 Jun 11.

Abstract

Ketoprofen, a nonsteroidal anti-inflammatory drug, inhibits the synthesis of prostaglandin. A novel hydrolase (Est25) with high ketoprofen specificity has previously been identified using a metagenomic library from environmental samples. Recombinant Est25 protein with a histidine tag at the N-terminus was expressed in Escherichia coli and purified in a homogenous form. Est25 was crystallized from 2.4 M sodium malonate pH 7.0 and X-ray diffraction data were collected to 1.49 A using synchrotron radiation. The crystals belong to the monoclinic space group C2, with unit-cell parameters a = 197.8, b = 95.2, c = 99.4 A, beta = 97.1 degrees.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Anti-Inflammatory Agents, Non-Steroidal / chemistry*
  • Anti-Inflammatory Agents, Non-Steroidal / metabolism
  • Crystallization
  • Crystallography, X-Ray
  • Hydrolases / chemistry
  • Hydrolases / isolation & purification
  • Hydrolases / metabolism
  • Ketoprofen / chemistry*
  • Ketoprofen / metabolism
  • Sterol Esterase / chemistry*
  • Sterol Esterase / isolation & purification*
  • Sterol Esterase / metabolism

Substances

  • Anti-Inflammatory Agents, Non-Steroidal
  • Ketoprofen
  • Hydrolases
  • Sterol Esterase