Literature DB >> 16061229

The role of firefly luciferase C-terminal domain in efficient coupling of adenylation and oxidative steps.

Keiichi Ayabe1, Tamotsu Zako, Hiroshi Ueda.   

Abstract

The N-terminal domain (N-domain) of the firefly luciferase from Photinus pyraris has weak luminescence activity, and shows a unique light emitting profile with very long rise time of more than several minutes. Through a sensitive assay of the reaction intermediate luciferyl-adenylate (LH2-AMP), we found that the slow increase in the N-domain luminescence faithfully reflected the concentration of dissociated LH2-AMP. No such correlation was observed for wild-type or mutant enzymes with short rise time, except one with longer rise time. The results suggest that the C-terminal domain plays an indispensable role in efficiently coupling adenylation and oxidative steps.

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Year:  2005        PMID: 16061229     DOI: 10.1016/j.febslet.2005.07.004

Source DB:  PubMed          Journal:  FEBS Lett        ISSN: 0014-5793            Impact factor:   4.124


  2 in total

1.  Rational design of a triple reporter gene for multimodality molecular imaging.

Authors:  Ya-Ju Hsieh; Luen Hwu; Chien-Chih Ke; Skye Hsin-Hsien Yeh; Chien-Feng Lin; Fu-Du Chen; Hsin-Ell Wang; Kang-Ping Lin; Ran-Chou Chen; Ren-Shyan Liu
Journal:  Biomed Res Int       Date:  2014-04-07       Impact factor: 3.411

2.  Mathematical Model of the Firefly Luciferase Complementation Assay Reveals a Non-Linear Relationship between the Detected Luminescence and the Affinity of the Protein Pair Being Analyzed.

Authors:  Renee Dale; Yuki Ohmuro-Matsuyama; Hiroshi Ueda; Naohiro Kato
Journal:  PLoS One       Date:  2016-02-17       Impact factor: 3.240

  2 in total

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