Lecocq R, Lamy F, Erneux C, Dumont J E
Interdisciplinary Research Institute (IRIBHN), Brussels, Belgium.
Biochem J. 1995 Feb 15;306 ( Pt 1)(Pt 1):147-51. doi: 10.1042/bj3060147.
A method is presented for the rapid purification of dog thyroid calcyphosine, a protein previously identified as a major substrate for cyclic AMP-dependent protein kinase in dog thyroid slices stimulated by thyrotropin [Lecocq, Lamy and Dumont (1979) Eur. J. Biochem. 102, 147-152]. The protein was previously identified as a spot on two-dimensional gels and is now purified in its native form by a procedure involving three chromatographic steps. Homogeneous calcyphosine identified by SDS/PAGE, immunoblotting and peptide sequencing can be obtained within 7 h. As for calmodulin, Ca(2+)-dependent conformational changes can be shown by Ca(2+)-dependent hydrophobic interaction chromatography using phenyl-Sepharose. Unlike calmodulin, calcyphosine is a substrate for protein kinase A.
本文介绍了一种快速纯化犬甲状腺钙磷蛋白的方法。该蛋白先前被鉴定为促甲状腺激素刺激的犬甲状腺切片中依赖环磷酸腺苷的蛋白激酶的主要底物[勒科克、拉米和杜蒙(1979年)《欧洲生物化学杂志》102卷,第147 - 152页]。该蛋白先前在二维凝胶上被鉴定为一个斑点,现在通过一个包含三个色谱步骤的程序以其天然形式进行纯化。通过SDS / PAGE、免疫印迹和肽测序鉴定的均一钙磷蛋白可在7小时内获得。至于钙调蛋白,使用苯基琼脂糖的钙依赖性疏水相互作用色谱可以显示钙依赖性构象变化。与钙调蛋白不同,钙磷蛋白是蛋白激酶A的底物。