| Literature DB >> 1633191 |
J M Reymann1, J M Rondeau, P Barth, M Jaquinod, A Van Dorsselaer, J F Biellmann.
Abstract
Aldose reductase (alditol: NADP+ 1-oxidoreductase, EC 1.1.1.21) has been purified from pig lens to homogeneity by a rapid and efficient three-step procedure involving poly(ethylene glycol) fractionation, ion-exchange chromatography and chromatofocusing. The homogeneity of the purified enzyme was examined by polyacrylamide gel electrophoresis under native and denaturing conditions, by isoelectric focusing and by high-performance liquid chromatography on a size-exclusion column. The highly purified enzyme is a monomeric protein with a molecular mass of 35,775 +/- 3 Da as determined by electrospray mass spectrometry (ESMS). This purification procedure is particularly suited for the preparation of triclinic single crystals of pig lens aldose reductase, which are currently used in X-ray studies of this enzyme.Entities:
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Year: 1992 PMID: 1633191 DOI: 10.1016/0167-4838(92)90119-x
Source DB: PubMed Journal: Biochim Biophys Acta ISSN: 0006-3002