Method for preparing medicine with proteinase inhibiting function and its detecting method
A protease inhibitor and protease technology, which is applied in the field of protein purification, can solve the problems of cumbersome detection technology operation and low detection sensitivity, and achieve the effects of cost reduction, high sensitivity and simplified process
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Embodiment 1
[0029] After Cohn's Component IV was dissolved with 20 times the weight of purified water, 37% sucrose and 0.38M sodium citrate were added as stabilizers for virus inactivation treatment. Then tributyl phosphate with a final concentration of 0.3% and Triton X-100 with a final concentration of 1.0% were added and incubated at 30° C. for 4 hours. After virus inactivation, adjust the pH to 6.5, reduce the ionic strength to 2.5mS / cm with water, and add it to a DEAE Sepharose Fast Flow chromatography column pre-balanced at pH 6.5. The target protein α1-PI was selectively eluted with 20mM sodium dihydrogen phosphate and 100mM sodium chloride solution. Increasing the concentration of sodium chloride can elute strongly adsorbed foreign proteins, including ceruloplasmin, from the ion-exchange chromatography column. DEAE Sepharose Fast Flow resin can be reused after being sterilized with 0.5M sodium hydroxide.
[0030] The eluate containing α1-PI was passed through a 10 kD ultrafiltra...
Embodiment 2
[0034] The dissolved Cohn's fraction IV was adjusted to pH 5.4 with 1M hydrochloric acid and ionic strength to 1.5mS / cm with water, and then added to a CM Sepharose Fast Flow column pre-equilibrated with 5mM sodium citrate (pH 5.4). Collect the effluent from the ion exchange resin, adjust the pH to 6.5, adjust the ionic strength to 2.5mS / cm, and add it to a DEAE Sepharose Fast Flow chromatography column pre-balanced with 20mM sodium dihydrogen phosphate solution (pH 6.5). Active α1-PI was selectively eluted using 20 mM sodium dihydrogen phosphate and 100 mM sodium chloride solution. In this example, 58.9 mg of α1-PI with a purity of 92.5% was purified from 5.34 g of fraction IV. The yield of active α1-PI was as high as 81.2%. Table 3 is the experimental data of this example.
[0035] Total protein (mg)
[0036] All the other are identical with embodiment 1.
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