Step size of the rotary proton motor in single F oF 1-ATP synthase from a thermoalkaliphilic bacterium by DCO-ALEX FRET

Progress in Biomedical Optics and Imaging - Proceedings of SPIE

Volumn 8228, Issue , 2012, Pages

  Hammann, Eva ^a   Zappe, Andrea ^a   Keis, Stefanie ^b   Ernst, Stefan ^a,c   Matthies, Doreen ^d   Meier, Thomas ^d   Cook, Gregory M ^b   Börsch, Michael ^a,c  

^a UNIVERSITY OF STUTTGART   (Germany)

^b UNIVERSITY OF OTAGO   (New Zealand)

^c JENA UNIVERSITY HOSPITAL   (Germany)

^d MAX PLANCK INSTITUTE OF BIOPHYSICS   (Germany)

Author keywords

c subunit rotation; Caldalkalibacillus thermarum strain TA2.A1; duty cycle optimized alternating laser excitation (DCO ALEX); F oF 1 ATP synthase; single molecule FRET

Indexed keywords

AMBIENT TEMPERATURES; ATP SYNTHASE; ATP-PRODUCING ENZYMES; CALDALKALIBACILLUS THERMARUM STRAIN TA2.A1; DUTY CYCLE-OPTIMIZED ALTERNATING LASER EXCITATION (DCO-ALEX); DWELL TIME; HIGH FLEXIBILITY; HIGH TEMPERATURE; MEMBRANE PROTEINS; MOTOR ACTIVITY; RESONANCE ENERGY TRANSFER; ROOM TEMPERATURE; SINGLE MOLECULE LEVEL; SINGLE-MOLECULE; STEP SIZE; THERMOPHILIC ENZYMES;

BACTERIA; BIOLOGICAL MEMBRANES; ENERGY TRANSFER; ENZYMES; ESCHERICHIA COLI; LASER EXCITATION; OPTICAL RESOLVING POWER; OPTIMIZATION; PROTEINS;

MOLECULES;

EID: 84857551617     PISSN: 16057422     EISSN: None     Source Type: Conference Proceeding    
DOI: 10.1117/12.907242     Document Type: Conference Paper

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