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无血清悬浮培养中重组人凝血因子IX的生产方法。

Approaches for recombinant human factor IX production in serum-free suspension cultures.

作者信息

do Amaral Robson Luis Ferraz, de Sousa Bomfim Aline, de Abreu-Neto Mário Soares, Picanço-Castro Virgínia, de Sousa Russo Elisa Maria, Covas Dimas Tadeu, Swiech Kamilla

机构信息

School of Pharmaceutical Sciences of Ribeirão Preto, University of São Paulo, Café Ave, w/n, Ribeirão Prêto, São Paulo State, CEP 14040-903, Brazil.

Regional Blood Center of Ribeirão Preto, Tenente Catão Roxo Street, 2501, Ribeirão Prêto, São Paulo State, CEP 14051-140, Brazil.

出版信息

Biotechnol Lett. 2016 Mar;38(3):385-94. doi: 10.1007/s10529-015-1991-1. Epub 2015 Nov 12.

Abstract

OBJECTIVE

To establish a serum-free suspension process for production of recombinant human factor IX (rhFIX) based on the human cell line HEK 293T by evaluating two approaches: (1) serum-free suspension adaptation of previously genetic modified cells (293T-FIX); and (2) genetic modification of cells already adapted to such conditions (293T/SF-FIX).

RESULTS

After 10 months, 293T-FIX cells had become adapted to FreeStyle 293 serum-free medium (SFM) in Erlenmeyer flasks. After 48 and 72 h of culture, 2.1 µg rhFIX/ml and 3.3 µg rhFIX/ml were produced, respectively. However, no biological activity was detected. In the second approach, wild-type 293T cells were adapted to the same SFM (adaptation process took only 2 months) and then genetically modified for rhFIX production. After 48 h of culture, rhFIX reached 1.5 µg/ml with a biological activity of 0.2 IU/ml, while after 72 h, the production was 2.4 µg/ml with a biological activity of 0.3 IU/ml.

CONCLUSION

The findings demonstrate that the best approach to establish an rhFIX production process in suspension SFM involves the genetic modification of cells already adapted to the final conditions. This approach is time saving and may better ensure the quality of the produced protein.

摘要

目的

通过评估两种方法,建立一种基于人细胞系HEK 293T的无血清悬浮培养生产重组人凝血因子IX(rhFIX)的工艺:(1)对先前经过基因改造的细胞(293T-FIX)进行无血清悬浮适应性培养;(2)对已适应此类条件的细胞(293T/SF-FIX)进行基因改造。

结果

10个月后,293T-FIX细胞在锥形瓶中适应了FreeStyle 293无血清培养基(SFM)。培养48小时和72小时后,分别产生了2.1μg rhFIX/ml和3.3μg rhFIX/ml。然而,未检测到生物活性。在第二种方法中,野生型293T细胞适应了相同的无血清培养基(适应过程仅需2个月),然后进行基因改造以生产rhFIX。培养48小时后,rhFIX达到1.5μg/ml,生物活性为0.2IU/ml,而培养72小时后,产量为2.4μg/ml,生物活性为0.3IU/ml。

结论

研究结果表明,在悬浮无血清培养基中建立rhFIX生产工艺的最佳方法是对已适应最终条件的细胞进行基因改造。这种方法节省时间,可能更好地确保所生产蛋白质的质量。

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