Literature DB >> 1633191

Purification and electrospray mass spectrometry of aldose reductase from pig lens.

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.

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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


  2 in total

1.  Binding of aldose reductase inhibitors: correlation of crystallographic and mass spectrometric studies.

Authors:  H Rogniaux; A Van Dorsselaer; P Barth; J F Biellmann; J Barbanton; M van Zandt; B Chevrier; E Howard; A Mitschler; N Potier; L Urzhumtseva; D Moras; A Podjarny
Journal:  J Am Soc Mass Spectrom       Date:  1999-07       Impact factor: 3.109

2.  Role of methionine in the active site of alpha-galactosidase from Trichoderma reesei.

Authors:  A M Kachurin; A M Golubev; M M Geisow; O S Veselkina; L S Isaeva-Ivanova; K N Neustroev
Journal:  Biochem J       Date:  1995-06-15       Impact factor: 3.857

  2 in total

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