Structural differences between the closed and open states of channelrhodopsin-2 as observed by EPR spectroscopy

FEBS Letters

Volumn 587, Issue 20, 2013, Pages 3309-3313

  Krause, Nils ^a   Engelhard, Christopher ^a   Heberle, Joachim ^a   Schlesinger, Ramona ^a   Bittl, Robert ^a  

^a FREIE UNIVERSITÄT BERLIN   (Germany)

Author keywords

EPR spectroscopy; Light activated cation channel; Membrane protein; Optogenetic; Photocycle; Rhodopsin

Indexed keywords

CATION CHANNEL; CHANNELRHODOPSIN 2; CYSTEINE; UNCLASSIFIED DRUG;

ARTICLE; COMPARATIVE STUDY; CONFORMATIONAL TRANSITION; CRYSTAL STRUCTURE; CRYSTALLOGRAPHY; ELECTRON SPIN RESONANCE; ILLUMINATION; INFRARED SPECTROSCOPY; ION CONDUCTANCE; PRIORITY JOURNAL; PROTEIN CONFORMATION; PROTEIN EXPRESSION; SPIN LABELING;

(1-OXYL-2,2,5,5-TETRAMETHYLPYRROLINE-3-METHYL)METHANETHIOSULFONATE SPIN LABEL; 2-(N-MORPHOLINO)ETHANESULFONIC ACID; BACTERIORHODOPSIN; BR; CHANNELRHODOPSIN 2; CHR2; CONTINUOUS WAVE ELECTRON PARAMAGNETIC RESONANCE; CW-EPR; DECYL-Β-D-MALTOSIDE; DEER; DM; DOUBLE ELECTRON-ELECTRON RESONANCE; ELECTRON PARAMAGNETIC RESONANCE; EPR; EPR SPECTROSCOPY; LIGHT-ACTIVATED CATION CHANNEL; MEMBRANE PROTEIN; MES; MTSL; OPTOGENETIC; PELDOR; PHOTOCYCLE; PULSED ELECTRON-ELECTRON DOUBLE RESONANCE; RHODOPSIN; SENSORY RHODOPSIN II; SRII;

ELECTRON SPIN RESONANCE SPECTROSCOPY; PROTEIN STRUCTURE, SECONDARY; PROTEIN STRUCTURE, TERTIARY; RHODOPSIN;

EID: 84884906995     PISSN: 00145793     EISSN: 18733468     Source Type: Journal    
DOI: 10.1016/j.febslet.2013.08.043     Document Type: Article

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