Park M H, Cooper H L, Folk J E
J Biol Chem. 1982 Jun 25;257(12):7217-22.
The major labeled constituent produced in cellular protein during the incubation of Chinese hamster ovary (CHO) cells with [3H]putrescine or [terminal methylenes-3H]spermidine was identified as hypusine (N epsilon -(4-amino-2-hydroxybutyl)lysine). This unusual amino acid was found to occur predominantly in one relatively acidic low molecular weight protein. When CHO cells were labeled with [4,5-3H)lysine, a small portion of the radioactivity of the cellular protein fraction, after release by proteolytic digestion or acid hydrolysis, chromatographed at the position of hypusine. Oxidative degradation of this isolated labeled material yielded labeled lysine, thus, providing evidence that lysine is the amino acid precursor of hypusine. Upon incubation of CHO cells with the metal chelator, alpha,alpha-dipyridyl, and either [4,5]3H]lysine or [terminal methylenes-3H]spermidine, label was incorporated into a protein-bound material, the chromatographic properties of which, after release by digestion, were found to be different from those of hypusine. This constituent of cell protein was identified as the unhydroxylated form of hypusine, deoxyhypusine (N epsilon -(4-aminobutyl)lysine). Evidence that the normal biosynthesis of hypusine proceeds through hydroxylation of deoxyhypusine was obtained by demonstration of conversion of protein-bound deoxyhypusine to protein-bound hypusine both in intact cells and in cell-free lysate. In the presence of the metal chelator, alpha,alpha-dipyridyl, deoxyhypusine accumulated in a single protein whose two dimensional electrophoretic properties were indistinguishable from those of the usual hypusine-containing protein. This finding supports the proposed mechanism in which peptide-bound lysine is converted to peptide-bound hypusine through hydroxylation of the transitory intermediate, deoxyhypusine.
在中国仓鼠卵巢(CHO)细胞与[3H]腐胺或[末端亚甲基-3H]亚精胺孵育期间,细胞蛋白质中产生的主要标记成分被鉴定为hypusine(Nε-(4-氨基-2-羟基丁基)赖氨酸)。发现这种不寻常的氨基酸主要存在于一种相对酸性的低分子量蛋白质中。当CHO细胞用[4,5-3H]赖氨酸标记时,细胞蛋白质部分经蛋白水解消化或酸水解释放后,一小部分放射性物质在hypusine的位置进行色谱分析。这种分离出的标记物质的氧化降解产生了标记的赖氨酸,因此,证明赖氨酸是hypusine的氨基酸前体。在用金属螯合剂α,α-联吡啶以及[4,5]3H]赖氨酸或[末端亚甲基-3H]亚精胺孵育CHO细胞后,标记物被掺入一种与蛋白质结合的物质中,经消化释放后,其色谱性质被发现与hypusine不同。细胞蛋白质的这种成分被鉴定为hypusine的未羟基化形式,脱氧hypusine(Nε-(4-氨基丁基)赖氨酸)。通过证明完整细胞和无细胞裂解物中蛋白质结合的脱氧hypusine向蛋白质结合的hypusine的转化,获得了hypusine正常生物合成通过脱氧hypusine羟基化进行的证据。在金属螯合剂α,α-联吡啶存在下,脱氧hypusine在一种单一蛋白质中积累,其二维电泳性质与通常含hypusine的蛋白质无法区分。这一发现支持了所提出的机制,即肽结合的赖氨酸通过瞬时中间体脱氧hypusine的羟基化转化为肽结合的hypusine。