Literature DB >> 7864802

Rapid purification and identification of calcyphosine, a Ca(2+)-binding protein phosphorylated by protein kinase A.

R Lecocq1, F Lamy, C Erneux, J E Dumont.   

Abstract

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.

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Year:  1995        PMID: 7864802      PMCID: PMC1136494          DOI: 10.1042/bj3060147

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  9 in total

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Review 3.  Use of two-dimensional gel electrophoresis and autoradiography as a tool in cell biology: the example of the thyroid and the liver.

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4.  Pattern of protein phosphorylation in intact stimulated cells: thyrotropin and dog thyroid.

Authors:  R Lecocq; F Lamy; J E Dumont
Journal:  Eur J Biochem       Date:  1979-12

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Authors:  A Lefort; R Lecocq; F Libert; F Lamy; S Swillens; G Vassart; J E Dumont
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