| Literature DB >> 21035690 |
Sarah E Webb1, Kelly L Rogers, Eric Karplus, Andrew L Miller.
Abstract
In this chapter, we describe the practical aspects of measuring [Ca(2+)] transients that are generated in a particular cytoplasmic domain, or within a specific organelle or its periorganellar environment, using bioluminescent, genetically encoded and targeted Ca(2+) reporters, especially those based on apoaequorin. We also list examples of the organisms, tissues, and cells that have been transfected with apoaequorin or an apoaequorin-BRET complex, as well as of the organelles and subcellular domains that have been specifically targeted with these bioluminescent Ca(2+) reporters. In addition, we summarize the various techniques used to load the apoaequorin cofactor, coelenterazine, and its analogs into cells, tissues, and intact organisms, and we describe recent advances in the detection and imaging technologies that are currently being used to measure and visualize the luminescence generated by the aequorin-Ca(2+) reaction within these various cytoplasmic domains and subcellular compartments.Entities:
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Year: 2010 PMID: 21035690 DOI: 10.1016/B978-0-12-374841-6.00010-4
Source DB: PubMed Journal: Methods Cell Biol ISSN: 0091-679X Impact factor: 1.441