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Partial purification and characterization of messenger RNA coding 14-3-2 protein from rat brain.

作者信息

Sakimura K, Araki K, Kushiya E, Takahashi Y

出版信息

J Neurochem. 1982 Aug;39(2):366-70. doi: 10.1111/j.1471-4159.1982.tb03957.x.

Abstract

14-3-2 Protein (neuron-specific enolase) is a neuron-specific protein. Using a reticulocyte lysate cell-free system for translation of 14-3-2 protein mRNA, we have partially purified this mRNA by several procedures, including formamide sucrose density centrifugation, formamide polyacrylamide gel electrophoresis (PAGE) and polyuridylic acid (poly(U))-Sepharose affinity chromatography. Using mRNA obtained by these procedures, we could increase the translation ratio of 14-3-2 protein synthesized/total soluble protein synthesized to 7.31%. The overall purification was 37.8-fold. The size of 14-3-2 protein mRNA appears to be about 19-20S, because translation activity of mRNA obtained by sucrose density gradient centrifugation or formamide PAGE was the most active in this RNA size.

摘要

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