Preparation of recombinant α-thrombin:: High-level expression of recombinant human prethrombin-2 and its activation by recombinant ecarin

被引:21
|
作者
Yonemura, H
Imamura, T
Soejima, K
Nakahara, Y
Morikawa, W
Ushio, Y
Kamachi, Y
Nakatake, H
Sugawara, K
Nakagaki, T
Nozaki, C [1 ]
机构
[1] Chemo Sero Therapeut Res Inst KAKETSUKEN, Dept Res 1, Kumamoto 8691298, Japan
[2] Chemo Sero Therapeut Res Inst KAKETSUKEN, Dept Appl Res, Kumamoto 8691298, Japan
来源
JOURNAL OF BIOCHEMISTRY | 2004年 / 135卷 / 05期
关键词
alpha-thrombin; ecarin; prethrombin-2; recombinant;
D O I
10.1093/jb/mvh070
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We have established a large-scale manufacturing system to produce recombinant human alpha-thrombin. In this system, a high yield of alpha-thrombin is prepared from prethrombin-2 activated by recombinant ecarin. We produced human prethrombin-2 using mouse myeloma cells and an expression plasmid carrying the chicken beta-actin promoter and mutant dihydrofolate reductase gene for gene amplification. To increase prethrombin-2 expression further, we performed fed-batch cultivation with the addition of vegetable peptone in 50 liters of suspension culture. After five feedings of vegetable peptone, the expression level of the recombinant prethrombin-2 reached 200 mug/ml. Subsequently, the recombinant prethrombin-2 could be activated to alpha-thrombin by recombinant ecarin expressed in a similar manner. Finally, recombinant alpha-thrombin was purified to homogeneity by affinity chromatography using a benzamidine-Sepharose gel. The yield from prethrombin-2 in culture medium was approximately 70%. The activity of the purified recombinant a-thrombin, including hydrolysis of a chromogenic substrate, release of fibrinopeptide A, and activation of protein C, was indistinguishable from that of plasma-derived alpha-thrombin. Our system is suitable for the large-scale production of recombinant alpha-thrombin, which can be used in place of clinically available alpha-thrombin derived from human or bovine plasma.
引用
收藏
页码:577 / 582
页数:6
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