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P Grandics

Publications and source records attributed to P Grandics.

5 recordsLinked to original sources

Integration of cell culture with continuous, on-line sterile downstream processing.

The development of an integrated system for the continuous, automated production of pure cell culture derived proteins is discussed. The system comprises a cell culture subunit for the continuous culture of mammalian cells and a purification subunit linked on-line to the cell culture subunit. The cells are compartmentalized and continuously perfused with culture medium. The cell culture medium leaving the bioreactor is perfused through a sterile immunoaffinity column that instantaneously removes the product from the culture fluid. This results in improved product quality because the product is quickly removed from the cell culture, thus minimizing contact with degradative enzymes. The culture medium, stripped from the secreted product, is recirculated into the bioreactor. The system allows simple, automated, and economical production of purified proteins with higher quality than that possible with current production methods. The integration also allows on-line, real-time process monitoring, thus simplifying process development and allowing more consistent production of biologics.

Animals

The goat blood binder of triamcinolone acetonide does not interfere with glucocorticoid receptor purification from mammary tissue.

The high affinity triamcinolone acetonide (TA) binder in goat blood was characterized in the context of our objective to purify glucocorticoid receptor from mammary tissue of the goat. A single class of binding sites was detected exhibiting an apparent equilibrium dissociation constant (Kd) of 1.3 X 10(-7) M, and the binding capacity was found to be 2200 fmol/mg serum protein. Steroid binding specificity studies revealed a unique preference for TA in steroid binding. Unlike the glucocorticoid receptor, the blood TA-binder is thermostable. DEAE-cellulose chromatography resolved the blood binder into two radioactivity peaks. On sucrose gradients, the [3H]TA binder sedimented at 8S. Gel filtration analysis demonstrated a single radioactivity peak exhibiting a Stokes radius of 47 A. From the hydrodynamic parameters an apparent Mr = 163,500 can be calculated for the blood binder. The blood TA binder displays negligible binding affinity for the steroid ligand of the deoxycorticosterone-derivatized affinity resin. These observations demonstrated that the goat blood TA-binding component, and the cytoplasmic glucocorticoid receptor from lactating goat mammary tissue are quite dissimilar entities and, therefore, the blood binder will not interfere with the purification of the glucocorticoid receptor.

Animals