Production of recombinant plant calmodulin and its use to detect calmodulin-binding proteins

被引:20
作者
Liao, BR
Zielinski, RE
机构
[1] Department of Plant Biology, University of Illinois, Urbana Illinois 61801
来源
METHODS IN CELL BIOLOGY, VOL 49 | 1995年 / 49卷
关键词
D O I
10.1016/S0091-679X(08)61475-2
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Calmodulin (CaM) is a major intracellular receptor for second messenger Ca2+ signals and is expressed in every cell of all eukaryotes, including plants. CaM transduces these signals by binding four Ca2+, and binding to and altering the activities of a variety of enzymatic, cytoskeletal, and structural proteins. This chapter presents various methods to detect plant CaM-binding proteins that exploit the simplicity with which recombinant plant CaM can be purified in milligram amounts from modest-sized cultures of induced Escherichia coli and labeled with a variety of reporters, which offer the advantages of sensitive detection of CaM-binding proteins and relatively low toxicity. The utility of these methods described for labeling CaM to use as a probe for detecting CaM-binding proteins can be illustrated by using two applications, which involve detecting CaM-binding activity in protein fractions after separation by sodium dodecyl sulfate–polyacrylamide gel electrophoresis (SDS–PAGE) and in induced lysates of recombinant bacteriophage harboring complementary DNA (cDNA) expression libraries. © 1995, Academic Press Inc.
引用
收藏
页码:487 / 500
页数:14
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