Firefly luciferase inhibition

J Photochem Photobiol B. 2010 Oct 5;101(1):1-8. doi: 10.1016/j.jphotobiol.2010.06.015. Epub 2010 Jul 3.

Abstract

Firefly luciferase (Luc) is the most studied of the luciferase enzymes and the mechanism and kinetics of the reactions catalyzed by this enzyme have been relatively well characterized. Luc catalyzes the bioluminescent reaction involving firefly luciferin (D-LH(2)), adenosine triphosphate (ATP), magnesium ion and molecular oxygen with the formation of an electronically excited species (oxyluciferin), inorganic pyrophosphate (PPi), carbon dioxide and adenosine monophosphate (AMP). Luc also catalyzes other non-luminescent reactions, which can interfere with the light production mechanism. Following electronic relaxation, the excited oxyluciferin emits radiation in the visible region of the electromagnetic spectrum (550-570 nm). Among the various possible compounds, several classes of inhibitory substances interfere with the activity of this enzyme: here, we consider substrate-related compounds, intermediates or products of the Luc catalyzed reactions, in addition to anesthetics and, fatty acids. This review summarizes the main inhibitors of Luc and the corresponding inhibition kinetic parameters.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Alkanes / chemistry
  • Anesthetics / chemistry
  • Animals
  • Benzothiazoles / chemistry
  • Catalysis
  • Enzyme Inhibitors / chemistry*
  • Fatty Acids / chemistry
  • Fireflies / enzymology
  • Indoles / chemistry
  • Indoles / metabolism
  • Luciferases, Firefly / antagonists & inhibitors
  • Luciferases, Firefly / metabolism*
  • Pyrazines / chemistry
  • Pyrazines / metabolism

Substances

  • Alkanes
  • Anesthetics
  • Benzothiazoles
  • Enzyme Inhibitors
  • Fatty Acids
  • Indoles
  • Pyrazines
  • oxyluciferin
  • Luciferases, Firefly
  • benzothiazole