Mass spectrometric analysis of rat liver cytosolic glutathione S-transferases: modifications are limited to N-terminal processing

• Published in: Biochemical journal 1995-05, Vol.308 ( Pt 1) (1), p.69-75
• Main Authors: Yeh, H I, Hsieh, C H, Wang, L Y, Tsai, S P, Hsu, H Y, Tam, M F
• Format: Article
• Language: English
• Subjects: Animals; Chromatography, Affinity; Chromatography, High Pressure Liquid; Female; Glutathione Transferase - chemistry; Isoenzymes - chemistry; Liver - enzymology; Male; Mass Spectrometry; Methionine - analogs & derivatives; Methionine - pharmacology; Molecular Weight; Rats; Rats, Sprague-Dawley
• ISSN: 0264-6021; 1470-8728
• DOI: 10.1042/bj3080069

Cytosolic glutathione S-transferases (GSTs) from rat livers were purified using an S-hexylglutathione affinity column. The GST subunits were resolved by reverse-phase HPLC and their molecular masses were determined by electrospray mass spectrometry. The major hepatic GSTs detected were subunits 1, 1', 2, 3 and 4, with molecular mass of 25,520, 25,473, 25,188, 25,782 and 25,571 Da respectively. Subunits 6, 7 and 10 are minor components, with molecular mass of 25,551, 23,308 and 25,211 Da respectively. Alternatively, the hepatic GSTs were purified using a glutathione affinity column. Subunits 1, 1', 2, 8 and 10 were eluted from this column with GSSG, the oxidized form of glutathione. Subunit 8 has a molecular mass of 25,553 Da. The remaining proteins on the glutathione affinity column were removed with glutathione and S-hexylglutathione. Subunits 2, 3, 4 and 6 could be detected in the eluate. We could not detect any significant difference in molecular mass between GSTs isolated from male and female rat livers. Cytosolic GSTs were isolated from livers of buthionine sulphoximine-treated female rats for MS analysis. The molecular masses obtained were identical to those determined for the controls.