Antibodies against the Calcium-Binding Protein
Author(s) -
Mei Chou,
Karl-Heinz Krause,
Kevin P. Campbell,
Kenneth G. Jensen,
Richard D. Sjölund
Publication year - 1989
Publication title -
plant physiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.554
H-Index - 312
eISSN - 1532-2548
pISSN - 0032-0889
DOI - 10.1104/pp.91.4.1259
Subject(s) - calsequestrin , endoplasmic reticulum , polyclonal antibodies , gel electrophoresis , monoclonal antibody , biochemistry , calcium , binding protein , biology , antibody , calcium binding protein , polyacrylamide gel electrophoresis , microbiology and biotechnology , microsome , chemistry , ryanodine receptor , in vitro , immunology , enzyme , organic chemistry , gene
Plant microsomes contain a protein clearly related to a calcium-binding protein, calsequestrin, originally found in the sarcoplasmic reticulum of muscle cells, responsible for the rapid release and uptake of Ca(2+) within the cells. The location and role of calsequestrin in plant cells is unknown. To generate monoclonal antibodies specific to plant calsequestrin, mice were immunized with a microsomal fraction from cultured cells of Streptanthus tortuosus (Brassicaceae). Two clones cross-reacted with one protein band with a molecular weight equal to that of calsequestrin (57 kilodaltons) by sodium dodecyl sulfate-polyacrylamide gel electrophoresis and immunoblotting. This band is able to bind (45)Ca(2+) and can be recognized by a polyclonal antibody against the canine cardiac muscle calsequestrin. Rabbit skeletal muscle calsequestrin cross-reacted with the plant monoclonal antibodies. The plant monoclonal antibodies generated here are specific to calsequestrin protein.
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