Literature DB >> 27930848

Brominated Luciferins Are Versatile Bioluminescent Probes.

Rachel C Steinhardt1, Colin M Rathbun1, Brandon T Krull1, Jason M Yu1, Yuhang Yang1, Brian D Nguyen1, Jake Kwon1, David C McCutcheon1, Krysten A Jones2, Filipp Furche1, Jennifer A Prescher1,2,3.   

Abstract

We report a set of brominated luciferins for bioluminescence imaging. These regioisomeric scaffolds were accessed by using a common synthetic route. All analogues produced light with firefly luciferase, although varying levels of emission were observed. Differences in photon output were analyzed by computation and photophysical measurements. The brightest brominated luciferin was further evaluated in cell and animal models. At low doses, the analogue outperformed the native substrate in cells. The remaining luciferins, although weak emitters with firefly luciferase, were inherently capable of light production and thus potential substrates for orthogonal mutant enzymes.
© 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  Appel's salt; bioluminescence; imaging; luciferase; luciferin

Mesh:

Substances:

Year:  2016        PMID: 27930848      PMCID: PMC5304417          DOI: 10.1002/cbic.201600564

Source DB:  PubMed          Journal:  Chembiochem        ISSN: 1439-4227            Impact factor:   3.164


  28 in total

Review 1.  Firefly luminescence: a historical perspective and recent developments.

Authors:  Hugo Fraga
Journal:  Photochem Photobiol Sci       Date:  2008-01-23       Impact factor: 3.982

2.  A "Caged" Luciferin for Imaging Cell-Cell Contacts.

Authors:  William B Porterfield; Krysten A Jones; David C McCutcheon; Jennifer A Prescher
Journal:  J Am Chem Soc       Date:  2015-07-06       Impact factor: 15.419

3.  Chemi- and bioluminescence of firefly luciferin.

Authors:  E H White; E Rapaport; T A Hopkins; H H Seliger
Journal:  J Am Chem Soc       Date:  1969-04-09       Impact factor: 15.419

4.  Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides.

Authors:  Adam F Littke; Lothar Schwarz; Gregory C Fu
Journal:  J Am Chem Soc       Date:  2002-06-05       Impact factor: 15.419

5.  Analogs of firefly luciferin. 3.

Authors:  E H White; H Wörther
Journal:  J Org Chem       Date:  1966-05       Impact factor: 4.354

6.  Identification of mutant firefly luciferases that efficiently utilize aminoluciferins.

Authors:  Katryn R Harwood; David M Mofford; Gadarla R Reddy; Stephen C Miller
Journal:  Chem Biol       Date:  2011-12-23

7.  Robust light emission from cyclic alkylaminoluciferin substrates for firefly luciferase.

Authors:  Gadarla Randheer Reddy; Walter C Thompson; Stephen C Miller
Journal:  J Am Chem Soc       Date:  2010-10-06       Impact factor: 15.419

8.  Firefly Luciferase Mutants Allow Substrate-Selective Bioluminescence Imaging in the Mouse Brain.

Authors:  Spencer T Adams; David M Mofford; G S Kiran Kumar Reddy; Stephen C Miller
Journal:  Angew Chem Int Ed Engl       Date:  2016-03-17       Impact factor: 15.336

9.  A synthetic luciferin improves bioluminescence imaging in live mice.

Authors:  Melanie S Evans; Joanna P Chaurette; Spencer T Adams; Gadarla R Reddy; Miranda A Paley; Neil Aronin; Jennifer A Prescher; Stephen C Miller
Journal:  Nat Methods       Date:  2014-02-09       Impact factor: 28.547

10.  Aminoluciferins extend firefly luciferase bioluminescence into the near-infrared and can be preferred substrates over D-luciferin.

Authors:  David M Mofford; Gadarla Randheer Reddy; Stephen C Miller
Journal:  J Am Chem Soc       Date:  2014-09-11       Impact factor: 15.419

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  15 in total

1.  Orthogonal Luciferase-Luciferin Pairs for Bioluminescence Imaging.

Authors:  Krysten A Jones; William B Porterfield; Colin M Rathbun; David C McCutcheon; Miranda A Paley; Jennifer A Prescher
Journal:  J Am Chem Soc       Date:  2017-02-03       Impact factor: 15.419

2.  Rapid Access to a Broad Range of 6'-Substituted Firefly Luciferin Analogues Reveals Surprising Emitters and Inhibitors.

Authors:  Deepak K Sharma; Spencer T Adams; Kate L Liebmann; Stephen C Miller
Journal:  Org Lett       Date:  2017-11-03       Impact factor: 6.005

3.  Statistical Coupling Analysis-Guided Library Design for the Discovery of Mutant Luciferases.

Authors:  Mira D Liu; Elliot A Warner; Charlotte E Morrissey; Caitlyn W Fick; Taia S Wu; Marya Y Ornelas; Gabriela V Ochoa; Brendan S Zhang; Colin M Rathbun; William B Porterfield; Jennifer A Prescher; Aaron M Leconte
Journal:  Biochemistry       Date:  2017-12-28       Impact factor: 3.162

Review 4.  Lessons Learned from Luminous Luciferins and Latent Luciferases.

Authors:  Stephen C Miller; David M Mofford; Spencer T Adams
Journal:  ACS Chem Biol       Date:  2018-02-19       Impact factor: 5.100

5.  Computational investigation into the fluorescence of luciferin analogues.

Authors:  Thom Vreven; Stephen C Miller
Journal:  J Comput Chem       Date:  2019-01-15       Impact factor: 3.376

6.  Building Biological Flashlights: Orthogonal Luciferases and Luciferins for in Vivo Imaging.

Authors:  Sierra J Williams; Jennifer A Prescher
Journal:  Acc Chem Res       Date:  2019-10-08       Impact factor: 22.384

7.  Pyridone Luciferins and Mutant Luciferases for Bioluminescence Imaging.

Authors:  Brendan S Zhang; Krysten A Jones; David C McCutcheon; Jennifer A Prescher
Journal:  Chembiochem       Date:  2018-01-31       Impact factor: 3.164

Review 8.  Seeing (and Using) the Light: Recent Developments in Bioluminescence Technology.

Authors:  Anna C Love; Jennifer A Prescher
Journal:  Cell Chem Biol       Date:  2020-08-13       Impact factor: 8.116

9.  Rapid Multicomponent Bioluminescence Imaging via Substrate Unmixing.

Authors:  Colin M Rathbun; Anastasia A Ionkina; Zi Yao; Krysten A Jones; William B Porterfield; Jennifer A Prescher
Journal:  ACS Chem Biol       Date:  2021-03-17       Impact factor: 5.100

10.  Orthogonal Bioluminescent Probes from Disubstituted Luciferins.

Authors:  Sierra J Williams; Clare S Hwang; Jennifer A Prescher
Journal:  Biochemistry       Date:  2021-02-18       Impact factor: 3.162

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