Seo H G, Fujii J, Soejima H, Niikawa N, Taniguchi N
Department of Biochemistry, Osaka University Medical School, Japan.
Biochem Biophys Res Commun. 1995 Mar 8;208(1):10-8. doi: 10.1006/bbrc.1995.1298.
We have cloned cDNAs encoding endothelial nitric oxide synthase (ecNOS) from a human fetal liver cDNA library. Overproduction of ecNOS in a baculovirus/insect cell expression system in conventional medium yielded a large amount of ecNOS protein localized in particulate components, but ecNOS activity was low. This activity was increased by addition of hemin to 2.5-fold. While a precursor for heme biosynthesis increased the activity, inhibitors of heme biosynthesis reduced the ecNOS activity to 50% without affecting the level of enzyme. After extraction of cells with 1% Triton X-100, ecNOS protein was purified by column chromatography. The resultant ecNOS required supplementation with cofactors for activity, but it did not require hemin. Binding of a protoporphyrin IX heme was confirmed by a pyridine hemochrome assay.
我们从人胎肝cDNA文库中克隆了编码内皮型一氧化氮合酶(ecNOS)的cDNA。在传统培养基中的杆状病毒/昆虫细胞表达系统中过量表达ecNOS,产生了大量定位于颗粒成分中的ecNOS蛋白,但ecNOS活性较低。通过添加血红素,该活性提高到了2.5倍。虽然血红素生物合成的前体增加了活性,但血红素生物合成的抑制剂将ecNOS活性降低到了50%,而不影响酶的水平。用1% Triton X-100提取细胞后,通过柱色谱法纯化ecNOS蛋白。所得的ecNOS需要补充辅因子以获得活性,但不需要血红素。通过吡啶血色原测定法证实了原卟啉IX血红素的结合。