Synthesis and phosphorylation of canine cardiac myosin in tissue-culture assessment of hypertrophying factors.

J Wilkman-Coffelt, C Fenner, D T Mason
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Abstract

Canine cardiac myosin, which was synthesized in a 14-day tissue culture, based on L-[3H] leucine incorporation, was precipitated with goat gamma G antimyosin (cardiac-specific) and analyzed on dodecylsulfate gels. Incorporation of 32PO4 into myosin chains occurring in culture was the same as that obtained in vivo and appeared to be coupled with translation. Removal of 32PO4 from myosin heavy chains with base treatment indicated the presence of phosphoserine and phosphothreonine in canine cardiac myosin heavy chains. Further acid hydrolysis confirmed the data. The system described here, i.e., analyses of 32PO4 and L[3H] leucine incorporation into myosin heavy chains, could be used as a system for assaying hypertrophying factors.

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犬心肌肌球蛋白的合成和磷酸化在组织培养肥厚因子评价中的应用。
以L-[3H]亮氨酸掺入为基础,在14天的组织培养中合成犬心肌肌球蛋白,用山羊γ G抗肌球蛋白(心脏特异性)沉淀,并在十二烷基硫酸凝胶上分析。在培养中32PO4进入肌球蛋白链的结果与在体内得到的结果相同,并且似乎与翻译相结合。碱基处理去除肌球蛋白重链中的32PO4表明犬心肌肌球蛋白重链中存在磷丝氨酸和磷苏氨酸。进一步的酸水解证实了这一数据。本文所描述的系统,即32PO4和L[3H]亮氨酸并入肌球蛋白重链的分析,可以用作分析肥厚因子的系统。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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