Identification of rat liver glutathione S‐transferase Yb subunits by partial N‐terminal sequencing after electroblotting of proteins onto a polyvinylidene difluoride membrane from an analytical isoelectric focusing gel

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Abstract
Rat liver glutathione S‐transferases were partially purified using S‐hexyl glutathione affinity chromatography, followed by native isoelectric focusing employing a pH 7–11 or pH 3–10 gradient. Proteins were excised and eluted from the gel for determination of subunit composition using sodium dodecyl sulfate‐polyacrylamide gel electrophoresis. In separate experiments, isoelectric focusing gels were equilibrated with a sodium dodecyl sulfate‐containing buffer at high pH, and proteins on the gel were electroblotted onto a polyvinylidene difluoride membrane, utilizing graphite plates as electrodes. The membrane‐bound proteins were visualized by Coomassie Brilliant Blue staining. The protein bands were then excised from the membrane and inserted into a gas phase sequenator for direct sequencing. N‐Terminal sequences thus determined were compared with published cDNA sequences. The isoelectric points (pIs) and positions on the isoelectric focusing gel of Yb1 Yb1, Yb1 Yb2 and Yb2 Yb2 subunits were determined. We have also located on the pH 3–10 focusing gel an N‐terminal blocked glutathione S‐transferase which has a molecular weight similar to Yb subunits.

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