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Elimination of a disulfide bond in the light chain of coagulation factor Ⅷ improves secretion of a BDD-FⅧ variant with an engineered inter-chain disulfide
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Ze-long LIU, Jing MIAO, Hui-ge QU, Xiao-yan CHI, Fu-xiang ZHU*
Acta Pharmaceutica Sinica | 2020, 55(1) : 54 - 59
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Acta Pharmaceutica Sinica | 2020, 55(1): 54-59
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Elimination of a disulfide bond in the light chain of coagulation factor Ⅷ improves secretion of a BDD-FⅧ variant with an engineered inter-chain disulfide
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Ze-long LIU, Jing MIAO, Hui-ge QU, Xiao-yan CHI, Fu-xiang ZHU*
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  • Life Science College, Ludong University, Yantai 264025, China
Published: 2020-01-12 doi: 10.16438/j.0513-4870.2019-0822
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The coagulation Ⅷ factor (FⅧ) contains eight pairs of disulfide bonds, which are involved in maintaining its structure and function. It has been demonstrated that the disulfide bond between Cys1899/Cys1903 of the A3 domain in the light chain impedes secretion. In our previous work, an engineered inter-chain disulfide in the B domain-deleted FⅧ (BDD-FⅧ) promoted heterodimer assembly and secretion of separately expressed heavy and light chains. In this study, we constructed two BDD-FⅧ variants, one of which contains an engineered inter-chain disulfide bond (F8C) between Met662 > Cys and Asp1828 > Cys mutations and another contains an endogenous A3 domain with a disrupted disulfide bond from F8C (F8CG) by replacement of Cys1899 and Cys1903 with Gly in F8C. We explored their function and secretion. By transducing F8C and F8CG into HEK293 and COS-7 cells, the formation of disulfide bonds and the secretion and coagulation activity of the two variants in the culture media and their binding affinity for von Willebrand factor (vWF) could be observed. The results show that variants F8C and F8CG are mainly the disulfide bonded heavy and light chain dimer, while the wild type BDD-FⅧ (F8) is dominated by the easily dissociated heavy and light chain dimer. The secretion and activity of F8C was significantly higher than that of F8, while the secretion and activity of F8CG was significantly higher than that of F8C. The vWF binding of the two variants is similar to F8. This indicates that the BDD-FⅧ variant F8CG may be attractive molecule for protein replacement and as a transgene in gene-therapy strategies. These findings are encouraging for future studies targeting disulfide bond elimination for further enhancement of FⅧ secretion.

coagulation factor Ⅷ  /  disulfide bond mutation  /  gene transfer  /  secretion
Ze-long LIU, Jing MIAO, Hui-ge QU, Xiao-yan CHI, Fu-xiang ZHU. Elimination of a disulfide bond in the light chain of coagulation factor Ⅷ improves secretion of a BDD-FⅧ variant with an engineered inter-chain disulfide[J]. Acta Pharmaceutica Sinica, 2020 , 55 (1) : 54 -59 . DOI: 10.16438/j.0513-4870.2019-0822
Year 2020 volume 55 Issue 1
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doi: 10.16438/j.0513-4870.2019-0822
  • Receive Date:2019-10-21
  • Online Date:2026-01-20
  • Published:2020-01-12
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  • Received:2019-10-21
  • Revised:2019-11-06
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    Life Science College, Ludong University, Yantai 264025, China
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表12种不同金属材料的力学参数

Family
属数
Number of
genus
种数
Number of
species
占总种数比例
Percentage of
total species (%)

Genus
种数
Number of
species
占总种数比例
Percentage of total
species (%)
鹅膏菌科Amanitaceae 2 11 5.26 鹅膏菌属 Amanita 10 4.78
小菇科 Mycenaceae 2 12 5.74 丝盖伞属 Inocybe 5 2.39
多孔菌科 Polyporaceae 8 14 6.70 蜡蘑属 Laccaria 5 2.39
红菇科 Russulaceae 3 23 11.00 小皮伞属 Marasmius 6 2.87
小菇属 Mycena 11 5.26
光柄菇属 Pluteus 5 2.39
红菇属 Russula 17 8.13
栓菌属 Trametes 5 2.39
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