Chu Pei-Hsuan, Huang Teng-Yi, Williams Jason, Stafford D W
Department of Biology, University of North Carolina, Chapel Hill, NC 27599-3280, USA.
Proc Natl Acad Sci U S A. 2006 Dec 19;103(51):19308-13. doi: 10.1073/pnas.0609401103. Epub 2006 Dec 12.
More than 21 million prescriptions for warfarin are written yearly in the U.S. Despite its importance, warfarin's target, vitamin K epoxide reductase (VKOR), has resisted purification since its identification in 1972. Here, we report its purification and reconstitution. HPC4, a calcium-specific antibody that recognizes a 12-aa tag, was used to purify and identify VKOR. Partial reconstitution is achieved on the column by washing with 0.4% dioleoylphosphatidylcholine/0.4% deoxycholate. Activity is completely recovered by dialysis against a buffer containing a reducing agent but lacking dioleoylphosphatidylcholine/deoxycholate. Removal of detergent from the eluted proteins apparently facilitates liposome formation. Purified recombinant VKOR with tag is approximately 21 kDa, as expected; fully active; and > 93% pure. The concentration of warfarin for 50% inhibition is the same for purified protein and microsomes. It has been reported that VKOR is a multisubunit enzyme. Our results, however, suggest that a single peptide can accomplish both the conversion of vitamin K epoxide to vitamin K and vitamin K to reduced vitamin K. This purification will allow further characterization of VKOR in relation to other components of the vitamin K cycle and should facilitate its structural determination.
在美国,每年开具的华法林处方超过2100万份。尽管华法林很重要,但其靶点维生素K环氧化物还原酶(VKOR)自1972年被发现以来一直难以纯化。在此,我们报告了它的纯化和重组过程。HPC4是一种识别12个氨基酸标签的钙特异性抗体,用于纯化和鉴定VKOR。通过用0.4%二油酰磷脂酰胆碱/0.4%脱氧胆酸盐洗涤,在柱上实现了部分重组。通过对含有还原剂但不含二油酰磷脂酰胆碱/脱氧胆酸盐的缓冲液进行透析,活性完全恢复。从洗脱的蛋白质中去除去污剂显然有助于脂质体的形成。带有标签的纯化重组VKOR约为21 kDa,符合预期;具有完全活性;纯度>93%。纯化的蛋白质和微粒体对华法林50%抑制的浓度相同。据报道,VKOR是一种多亚基酶。然而,我们的结果表明,单一肽可以完成维生素K环氧化物向维生素K以及维生素K向还原型维生素K的转化。这种纯化将允许进一步表征VKOR与维生素K循环的其他成分的关系,并应有助于其结构测定。