Literature DB >> 21035690

The use of aequorins to record and visualize Ca(2+) dynamics: from subcellular microdomains to whole organisms.

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.
Copyright © 2010 Elsevier Inc. All rights reserved.

Entities:  

Mesh:

Substances:

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


  6 in total

1.  GAP, an aequorin-based fluorescent indicator for imaging Ca2+ in organelles.

Authors:  Arancha Rodriguez-Garcia; Jonathan Rojo-Ruiz; Paloma Navas-Navarro; Francisco Javier Aulestia; Sonia Gallego-Sandin; Javier Garcia-Sancho; Maria Teresa Alonso
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-05       Impact factor: 11.205

Review 2.  Visualization of Ca²+ signaling during embryonic skeletal muscle formation in vertebrates.

Authors:  Sarah E Webb; Andrew L Miller
Journal:  Cold Spring Harb Perspect Biol       Date:  2011-02-01       Impact factor: 10.005

3.  Ca2+ release via two-pore channel type 2 (TPC2) is required for slow muscle cell myofibrillogenesis and myotomal patterning in intact zebrafish embryos.

Authors:  Jeffrey J Kelu; Sarah E Webb; John Parrington; Antony Galione; Andrew L Miller
Journal:  Dev Biol       Date:  2017-04-06       Impact factor: 3.582

4.  Subcellular calcium measurements in mammalian cells using jellyfish photoprotein aequorin-based probes.

Authors:  Massimo Bonora; Carlotta Giorgi; Angela Bononi; Saverio Marchi; Simone Patergnani; Alessandro Rimessi; Rosario Rizzuto; Paolo Pinton
Journal:  Nat Protoc       Date:  2013-10-10       Impact factor: 13.491

5.  Imaging Ca(2+) activity in mammalian cells and zebrafish with a novel red-emitting aequorin variant.

Authors:  Adil Bakayan; Beatriz Domingo; Atsushi Miyawaki; Juan Llopis
Journal:  Pflugers Arch       Date:  2014-10-31       Impact factor: 3.657

6.  Imaging long distance propagating calcium signals in intact plant leaves with the BRET-based GFP-aequorin reporter.

Authors:  Tou Cheu Xiong; Elsa Ronzier; Frédéric Sanchez; Claire Corratgé-Faillie; Christian Mazars; Jean-Baptiste Thibaud
Journal:  Front Plant Sci       Date:  2014-02-18       Impact factor: 5.753

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.