Literature DB >> 2871634

Bioluminescence in the sea: photoprotein systems.

O Shimomura.   

Abstract

Photoproteins are the primary reactants of the light-emitting reactions of various bioluminescent organisms. A photoprotein emits light in proportion to its amount, like a luciferin, but its light-emitting reaction does not require a luciferase. There are about two dozen types of bioluminescent organisms for which substantial biochemical knowledge is presently available, and about one third of them involve photoproteins. Most photoproteins are found in marine organisms. There are various types of photoproteins: the photoproteins of coelenterates, ctenophores and radiolarians require Ca2+ to trigger their luminescence; the photoproteins of the bivalve Pholas and of the scale worm appear to involve superoxide radicals and O2 in their light-emitting reactions; the photoprotein of euphausiid shrimps emits light only in the presence of a special fluorescent compound; the photoprotein of the millipede Luminodesmus, the only known example of terrestrial origin, requires ATP and Mg2+ to emit light. The Ca2+-sensitive photoproteins of coelenterates have been most frequently studied and most widely used. Therefore, they are overwhelmingly popular compared with other types. All coelenterate photoproteins, including aequorin, halistaurin, obelin and phialidin, have relative molecular masses close to 20 000, contain an identical functional group, and emit blue light in aqueous solution when a trace of Ca2+ is added, in the presence or absence of molecular oxygen. Aequorin contains an oxygenated form of coelenterazine in its functional group. When Ca2+ is added, aequorin decomposes into three parts, i.e., apo-aequorin, coelenteramide and CO2, accompanied by the emission of light. Apo-aequorin can be reconstituted into active aequorin indistinguishable from the original sample, by incubation with an excess of coelenterazine in a buffer containing 5 mM-EDTA and a trace of 2-mercaptoethanol, even at 0 degree C. Thus, aequorin and other coelenterate photoproteins can be luminesced and recharged repeatedly. The regeneration of coelenterate photoproteins in this manner probably takes place in vivo, utilizing stored coelenterazine. The photoproteins of coelenterates, and their chemically modified forms, are useful in measuring and monitoring calcium ions in biological systems, especially in single cells.

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Year:  1985        PMID: 2871634

Source DB:  PubMed          Journal:  Symp Soc Exp Biol        ISSN: 0081-1386


  16 in total

Review 1.  Molecular enigma of multicolor bioluminescence of firefly luciferase.

Authors:  Saman Hosseinkhani
Journal:  Cell Mol Life Sci       Date:  2010-12-28       Impact factor: 9.261

2.  Crystal structure of obelin after Ca2+-triggered bioluminescence suggests neutral coelenteramide as the primary excited state.

Authors:  Zhi-Jie Liu; Galina A Stepanyuk; Eugene S Vysotski; John Lee; Svetlana V Markova; Natalia P Malikova; Bi-Cheng Wang
Journal:  Proc Natl Acad Sci U S A       Date:  2006-02-08       Impact factor: 11.205

Review 3.  Firefly luciferase: an adenylate-forming enzyme for multicatalytic functions.

Authors:  Satoshi Inouye
Journal:  Cell Mol Life Sci       Date:  2009-10-27       Impact factor: 9.261

4.  Formation of the Ca2+-activated photoprotein obelin from apo-obelin and mRNA inside human neutrophils.

Authors:  A K Campbell; A K Patel; Z S Razavi; F McCapra
Journal:  Biochem J       Date:  1988-05-15       Impact factor: 3.857

5.  Targeting the Cytochrome bc1 Complex of Leishmania Parasites for Discovery of Novel Drugs.

Authors:  Diana Ortiz; Isaac Forquer; Jan Boitz; Radika Soysa; Carolyn Elya; Audrey Fulwiler; Aaron Nilsen; Tamsen Polley; Michael K Riscoe; Buddy Ullman; Scott M Landfear
Journal:  Antimicrob Agents Chemother       Date:  2016-07-22       Impact factor: 5.191

6.  Cause of spectral variation in the luminescence of semisynthetic aequorins.

Authors:  O Shimomura
Journal:  Biochem J       Date:  1995-03-01       Impact factor: 3.857

7.  Light-emitting channelrhodopsins for combined optogenetic and chemical-genetic control of neurons.

Authors:  Ken Berglund; Elisabeth Birkner; George J Augustine; Ute Hochgeschwender
Journal:  PLoS One       Date:  2013-03-27       Impact factor: 3.240

8.  Genomic organization, evolution, and expression of photoprotein and opsin genes in Mnemiopsis leidyi: a new view of ctenophore photocytes.

Authors:  Christine E Schnitzler; Kevin Pang; Meghan L Powers; Adam M Reitzel; Joseph F Ryan; David Simmons; Takashi Tada; Morgan Park; Jyoti Gupta; Shelise Y Brooks; Robert W Blakesley; Shozo Yokoyama; Steven Hd Haddock; Mark Q Martindale; Andreas D Baxevanis
Journal:  BMC Biol       Date:  2012-12-21       Impact factor: 7.431

Review 9.  Genetically-encoded tools for cAMP probing and modulation in living systems.

Authors:  Valeriy M Paramonov; Veronika Mamaeva; Cecilia Sahlgren; Adolfo Rivero-Müller
Journal:  Front Pharmacol       Date:  2015-09-15       Impact factor: 5.810

Review 10.  Bioluminescence imaging: a shining future for cardiac regeneration.

Authors:  Santiago Roura; Carolina Gálvez-Montón; Antoni Bayes-Genis
Journal:  J Cell Mol Med       Date:  2013-02-12       Impact factor: 5.310

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