Moore A, Boulton A P, Heid H W, Jarasch E D, Craig R K
Eur J Biochem. 1985 Nov 4;152(3):729-37. doi: 10.1111/j.1432-1033.1985.tb09254.x.
A serine-specific casein kinase, an integral membrane protein of the lactating guinea-pig mammary gland, has been purified from a Golgi-enriched membrane fraction, using a combination of sucrose gradient centrifugation and chromatography on ATP-agarose. The enzyme comprises a polypeptide of estimated Mr 74 000 as judged by sodium dodecyl sulphate/polyacrylamide gel electrophoresis, compared with a monomer Mr of 50 000 as determined by sucrose gradient centrifugation in the presence of 500 mM NaCl and 0.1% Triton X-100. Kinetic studies show that the purified enzyme exhibits kinetic constants distinctly different from the rabbit reticulocyte casein kinases I and II, whilst polyclonal antisera raised against the mammary gland enzyme did not cross-react with soluble liver or reticulocyte protein kinase activities. Immunoblotting and immunocytochemical analyses demonstrate the mammary gland enzyme's apparently unique location in lactating mammary gland tissue. Comparative studies with polyclonal antisera raised against bovine galactosyltransferase, show that casein kinase and galactosyltransferase have a similar intracellular localisation in the lactating mammary gland as judged by immunocytochemistry at the light level, but that casein kinase was unique to mammary gland whereas galactosyltransferase could be found in other tissues. The results extended our earlier observations which suggest a Golgi location for casein kinase, and demonstrate that future studies using this enzyme may well prove advantageous for the study of intracellular mechanisms involved in the biogenesis of organelles, in this instance the Golgi apparatus.
一种丝氨酸特异性酪蛋白激酶是泌乳豚鼠乳腺的一种整合膜蛋白,已通过蔗糖梯度离心和ATP-琼脂糖柱层析相结合的方法,从富含高尔基体的膜组分中纯化出来。通过十二烷基硫酸钠/聚丙烯酰胺凝胶电泳判断,该酶由一条估计分子量为74000的多肽组成,而在500 mM氯化钠和0.1% Triton X-100存在下通过蔗糖梯度离心测定的单体分子量为50000。动力学研究表明,纯化后的酶表现出与兔网织红细胞酪蛋白激酶I和II明显不同的动力学常数,而针对乳腺酶产生的多克隆抗血清与可溶性肝或网织红细胞蛋白激酶活性不发生交叉反应。免疫印迹和免疫细胞化学分析表明,该乳腺酶在泌乳乳腺组织中的定位明显独特。与针对牛半乳糖基转移酶产生的多克隆抗血清进行的比较研究表明,从光镜水平的免疫细胞化学判断,酪蛋白激酶和半乳糖基转移酶在泌乳乳腺中具有相似的细胞内定位,但酪蛋白激酶是乳腺特有的,而半乳糖基转移酶可在其他组织中发现。这些结果扩展了我们早期的观察结果,即提示酪蛋白激酶位于高尔基体,并证明使用这种酶进行的未来研究可能对研究细胞器生物发生过程中涉及的细胞内机制(在这种情况下是高尔基体)非常有利。