Unique modification of human heart glycerol 3-phosphate dehydrogenase by blue agarose |
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Authors: | J F McGinnis |
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Affiliation: | 1. Department of Anatomy, Mental Retardation Research Center, School of Medicine University of California, Los Angeles, California 90024 USA;2. Department of Obstetrics and Gynecology, Mental Retardation Research Center, School of Medicine University of California, Los Angeles, California 90024 USA |
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Abstract: | The major form of glycerol phosphate dehydrogenase in human heart (GPDH-1) is a minor form (less than 15%) in brain and other tissues and is extremely labile. After GPDH-1 was eluted from an agarose column to which Cibacron blue F3GA had been covalently linked, (a) it was no longer labile (t 1/2 at 40 degrees C changed from 1.6 min to greater than 180 min); (b) it could now be stained for activity on native gels following electro-phoresis; and (c) it now migrated with the bromphenol blue dye front. The results suggest that this stabilized form of GPDH-1 is due to the covalent binding of charged ligands from the column and that this technique may be useful for studying the molecular structure and/or the active site of GPHD-1 and possibly of other enzymes which bind to blue agarose. |
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