Characterization and purification of kinase activities against Arabidopsis COP9 signalosome subunit 7

被引:5
作者
Malec, Przemyslaw
Chamovitz, Daniel A. [1 ]
机构
[1] Tel Aviv Univ, Dept Plant Sci, IL-69978 Tel Aviv, Israel
[2] Jagiellonian Univ, Dept Physiol & Biochem Plants, Fac Biotechnol, PL-30387 Krakow, Poland
关键词
D O I
10.1560/D63A-QF35-RGEB-NRMQ
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The COP9 signalosome (CSN) is a multisubunit protein complex that intersects the ubiquitin (Ub)-proteasome pathway at several junctions. The CSN associates with several protein kinases that target key regulatory proteins that themselves are targets for Ub-dependent degradation, and several subunits themselves are phosphoproteins. We previously reported that Arabidopsis CSN7 is a phosphoprotein. To identify the kinases responsible for CSN7 phosphorylation, we biochemically purified CSN7-kinsae activities from cauliflower through a four-step purification procedure that resulted in a ca. 300-fold enrichment. One of these activities is Ca2+ dependent, while the second is not. Peptide fingerprint analysis of the purified proteins identified three putative CSN7 kinases.
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收藏
页码:239 / 246
页数:8
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