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Published on: January 30, 2018
Mammalian complex III heme dynamics studied with pump-probe spectroscopy and red light illuminations
Sean P O'Connor1, Samantha M Powell2,3, John M Rickman4
1Department of Physics and Astronomy, Texas A&M University, College Station, TX 77843, USA.
This study investigated photobiomodulation (PBM) mechanisms using transient absorption spectroscopy on porcine complex III. Red light did not significantly alter heme dynamics, ruling out PBM effects via axial ligand photodissociation.
Area of Science:
- Biophysics
- Cellular Mechanisms
- Spectroscopy
Background:
- Photobiomodulation (PBM) mechanisms remain unclear.
- Understanding PBM requires studying molecular interactions with light.
- Complex III (C-III) is a key component of the electron transport chain.
Purpose of the Study:
- To investigate the effect of red light on the heme dynamics of porcine C-III.
- To determine if continuous wave laser coupled transient absorption spectroscopy (CW-TAS) can detect PBM effects.
- To elucidate the molecular mechanisms of PBM initiation.
Main Methods:
- Characterization of porcine C-III using transient absorption spectroscopy (TAS).
- Application of a novel continuous wave laser coupled TAS (CW-TAS) procedure.
- Analysis of heme dynamics in the c1 reduced state of C-III under red light (635 nm, 4.7 mW/cm2).
Main Results:
- Vibrational cooling time constant for the oxidized state: 3.3 ± 0.3 ps.
- Axial ligand rebinding time constant for the c1 reduced state: 4.9 ± 0.4 ps.
- No significant changes in C-III heme dynamics were observed using CW-TAS.
Conclusions:
- The applied red light (635 nm, 4.7 mW/cm2) does not induce photobiomodulation (PBM) effects on C-III heme dynamics.
- Photodissociation of the axial ligand of C-III is not a mechanism for PBM initiation under these conditions.
- Further research is needed to fully understand PBM initiation mechanisms.
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