Literature DB >> 19957126

Photo-activatable probes for the analysis of receptor function in living cells.

Wen-Hong Li1.   

Abstract

Photo-activatable (caged) probes are powerful research tools for biological investigation. The superb maneuverability of a light beam allows researchers to activate caged probes with pinpoint accuracy. Recent developments in caging chemistry and two-photon excitation technique further enhance our capability to perform photo-uncaging with even higher spatial and temporal resolution, offering new photonic approaches to study cell signaling dynamics in greater detail. Here we present a sample method that combines the techniques of photo-activation and digital fluorescence microscopy to assay an important class of intracellular receptors for the second messenger D-myo-inositol 1,4,5-trisphosphate (Ins(1,4,5)P(3), or IP(3)). The imaging assay is performed in fully intact living cells using a caged and cell membrane permeable ester derivative of IP(3), cm-IP(3)/PM.

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Year:  2010        PMID: 19957126      PMCID: PMC5636004          DOI: 10.1007/978-1-60761-404-3_6

Source DB:  PubMed          Journal:  Methods Mol Biol        ISSN: 1064-3745


  22 in total

1.  Rapid photolytic release of adenosine 5'-triphosphate from a protected analogue: utilization by the Na:K pump of human red blood cell ghosts.

Authors:  J H Kaplan; B Forbush; J F Hoffman
Journal:  Biochemistry       Date:  1978-05-16       Impact factor: 3.162

2.  Infrared-LAMP: two-photon uncaging and imaging of gap junctional communication in three dimensions.

Authors:  Kenneth Dakin; Wen-hong Li
Journal:  Nat Methods       Date:  2006-12       Impact factor: 28.547

3.  Measuring calcium signaling using genetically targetable fluorescent indicators.

Authors:  Amy E Palmer; Roger Y Tsien
Journal:  Nat Protoc       Date:  2006       Impact factor: 13.491

4.  The nitrodibenzofuran chromophore: a new caging group for ultra-efficient photolysis in living cells.

Authors:  Atsuya Momotake; Nicolas Lindegger; Ernst Niggli; Robert J Barsotti; Graham C R Ellis-Davies
Journal:  Nat Methods       Date:  2006-01       Impact factor: 28.547

5.  Cell-permeant caged InsP3 ester shows that Ca2+ spike frequency can optimize gene expression.

Authors:  W Li; J Llopis; M Whitney; G Zlokarnik; R Y Tsien
Journal:  Nature       Date:  1998-04-30       Impact factor: 49.962

6.  Photolabile precursors of inositol phosphates. Preparation and properties of 1-(2-nitrophenyl)ethyl esters of myo-inositol 1,4,5-trisphosphate.

Authors:  J W Walker; J Feeney; D R Trentham
Journal:  Biochemistry       Date:  1989-04-18       Impact factor: 3.162

7.  Co-expression in vertebrate tissues and cell lines of multiple inositol 1,4,5-trisphosphate (InsP3) receptors with distinct affinities for InsP3.

Authors:  C L Newton; G A Mignery; T C Südhof
Journal:  J Biol Chem       Date:  1994-11-18       Impact factor: 5.157

8.  The efficiency of two-photon photolysis of a "caged" fluorophore, o-1-(2-nitrophenyl)ethylpyranine, in relation to photodamage of synaptic terminals.

Authors:  Nikolai I Kiskin; Rod Chillingworth; James A McCray; David Piston; David Ogden
Journal:  Eur Biophys J       Date:  2002-02       Impact factor: 1.733

9.  Caged cyclic ADP-ribose. Synthesis and use.

Authors:  R Aarhus; K Gee; H C Lee
Journal:  J Biol Chem       Date:  1995-03-31       Impact factor: 5.157

10.  New caged coumarin fluorophores with extraordinary uncaging cross sections suitable for biological imaging applications.

Authors:  YuRui Zhao; Quan Zheng; Kenneth Dakin; Ke Xu; Manuel L Martinez; Wen-Hong Li
Journal:  J Am Chem Soc       Date:  2004-04-14       Impact factor: 15.419

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