4.5 Review

New red-fluorescent calcium indicators for optogenetics, photoactivation and multi-color imaging

Journal

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH
Volume 1843, Issue 10, Pages 2284-2306

Publisher

ELSEVIER
DOI: 10.1016/j.bbamcr.2014.03.010

Keywords

Calcium; Fluorescence; Genetically encoded calcium indicator (GECI); Spectral cross-talk; Nanobiosensor

Funding

  1. Agence Nationale de la Recherche (ANR PNANO) [ANR P3N]
  2. European Union
  3. Large National Infrastructure FranceBiolmaging (FBI) [ANR-10-INSB-04]
  4. Investments for the future [ANR-10-LABX-54 MEMO LIFE, ANR-11-IDEX-001-02-PSL]

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Most chemical and, with only a few exceptions, all genetically encoded fluorimetric calcium (Ca2+) indicators (GECIs) emit green fluorescence. Many of these probes are compatible with red-emitting cell- or organelle markers. But the bulk of available fluorescent-protein constructs and transgenic animals incorporate green or yellow fluorescent protein (GFP and YFP respectively). This is, in part, not only heritage from the tendency to aggregate of early-generation red-emitting FPs, and due to their complicated photochemistry, but also resulting from the compatibility of green-fluorescent probes with standard instrumentation readily available in most laboratories and core imaging facilities. Photochemical constraints like limited water solubility and low quantum yield have contributed to the relative paucity of red-emitting Ca2+ probes compared to their green counterparts, too. The increasing use of GFP and GFP-based functional reporters, together with recent developments in optogenetics, photostimulation and super-resolution microscopies, has intensified the quest for red-emitting Ca2+ probes. In response to this demand more red-emitting chemical and FP-based Ca2+ -sensitive indicators have been developed since 2009 than in the thirty years before. In this topical review, we survey the physicochemical properties of these red-emitting Ca2+ probes and discuss their utility for biological Ca2+ imaging. Using the spectral separability index X-ijk (Oheim M., 2010. Methods in Molecular Biology 591: 3-16) we evaluate their performance for multi-color excitation/emission experiments, involving the identification of morphological landmarks with GFP/YFP and detecting Ca2+-dependent fluorescence in the red spectral band. We also establish a catalog of criteria for evaluating Ca2+ indicators that ideally should be made available for each probe. This article is part of a Special Issue entitled: Calcium signaling in health and disease. Guest Editors: Geert Bultynck, Jacques Haiech, Claus W. Heizmann, Joachim Krebs, and Marc Moreau. (C) 2014 Elsevier B.V. All rights reserved.

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