Burkart T, Siegrist H P, Herschkowitz N N, Wiesmann U N
Biochim Biophys Acta. 1977 Aug 11;483(2):303-11. doi: 10.1016/0005-2744(77)90058-4.
An optimized in vitro assay of 3'-phosphoadenylysulfate:galactosylceramide 3'-sulfotransferase (EC 2.8.2.11, galactosylceramide sulfotransferase, formerly known as galactocerebroside sulfotransferase) activity is presented, that can be used in crude homogenate of brain tissue of various developmental stages. The enzyme activity is determined by measuring the [35S]sulfatides formed by the enzymic transfer of [35S]sulfate from 3'-phosphoadenoside 5'-phospho [35S]sulfate to galactosylceramides. The sulfatide formation at 30 degrees C is linear up to 30 min and up to a protein concentration of 1 mg per 0.5 ml assay volume. The presence of 0.4% Triton X-100 and 50 micrometer exogenous bovine cerebrosides are optimal for enzyme activity. The pH optimum of the reaction is at pH 6.5 using 0.1 M imidazole buffer. The enzyme reaction is stimulated by NaCl, KCl, MgCl2, CaCl2, MnCl2, ATP and inhibited by ADP. The developmental enzyme activity pattern of mouse brain is the same, if derived from homogenates and microsomes, respectively, under our assay conditions.
本文介绍了一种优化的体外测定3'-磷酸腺苷酰硫酸:半乳糖神经酰胺3'-磺基转移酶(EC 2.8.2.11,半乳糖神经酰胺磺基转移酶,以前称为半乳糖脑苷脂磺基转移酶)活性的方法,该方法可用于不同发育阶段脑组织的粗匀浆。通过测量由[35S]硫酸从3'-磷酸腺苷5'-磷酸[35S]硫酸盐酶促转移至半乳糖神经酰胺形成的[35S]硫脂来测定酶活性。在30℃下,硫脂形成在30分钟内呈线性,且在每0.5 ml测定体积中蛋白质浓度达1 mg时也呈线性。0.4% Triton X-100和50微米外源性牛脑苷脂的存在对酶活性最为适宜。使用0.1 M咪唑缓冲液时,反应的最适pH为6.5。酶反应受NaCl、KCl、MgCl2、CaCl2、MnCl2、ATP刺激,受ADP抑制。在我们的测定条件下,分别从小鼠脑匀浆和微粒体获得的小鼠脑发育酶活性模式相同。