4.5 Article

Structural basis for the phototoxicity of the fluorescent protein KillerRed

Journal

FEBS LETTERS
Volume 583, Issue 17, Pages 2839-2842

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.febslet.2009.07.041

Keywords

CALI; Fluorescent proteins; X-ray crystallography; Reactive oxygen species; Solvent channel

Funding

  1. CEA
  2. ANR [ANR-07-BLAN-0107-01, ANR06-PCVI-0022-02]

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The red fluorescent protein KillerRed, engineered from the hydrozoan chromoprotein anm2CP, has been reported to induce strong cytotoxicity through the chromophore assisted light inactivation (CALI) effect. Here, we present the X-ray structures of KillerRed in its native and bleached states. A long water-filled channel is revealed, connecting the methylene bridge of the chromophore to the solvent. This channel facilitates the transit of oxygen and of reactive oxygen species (ROS) formed by reaction with the excited chromophore. The functional roles of key mutations used to produce KillerRed are discussed, strong chromophore distortions in the bleached state are revealed, and mechanisms for ROS production and self protection are proposed. The presence of a partially mature, photo-resistant, green-emitting state is characterized, which accounts for enhanced CALI by pre-bleached KillerRed. (C) 2009 Federation of European Biochemical Societies. Published by Elsevier B. V. All rights reserved.

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