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Investigation of reaction mechanisms of cytochrome c and mitochondria with transient absorption spectroscopy

机译:瞬态吸收光谱法研究细胞色素c与线粒体的反应机理

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We performed Transient Absorption Spectroscopy (TAS) on samples of cytochrome c in its reduced and oxidized statesas well as mitochondria, and we use kinetic analysis to determine the decay rates of the transients. We also tested thesamples following red light exposures to determine if there were any changes in transient decay rates. Mitochondria wereisolated from hTERT-RPE1 cells and were tested in a glutamate buffer solution while cytochrome c was tested in a SodiumPhosphate solution (Na_2PO_4). Femtosecond TAS was performed with a pump pulse with wavelength centered at 418 nmand a supercontinuum probe pulse with a spectrum between 440 and 760 nm. Red light illuminations were performed witha 635 nm continuous wave light source at an intensity of 1.6 mW/cm~2 for 0.5 hours. We find transients and kinetic decayrates for reduced and oxidized cytochrome c that are consistent with previous literature. However, we do not find anytransients for mitochondria under our current TAS testing parameters, and we expect that this may be due to low Signalto-Noise ratio or choice of pump wavelength.
机译:我们对处于还原态和氧化态\ r \ nas以及线粒体的细胞色素c样品进行了瞬态吸收光谱(TAS),并使用动力学分析来确定瞬态的衰减率。我们还测试了红光照射后的样本,以确定瞬态衰减率是否有任何变化。线粒体从hTERT-RPE1细胞中分离出来,并在谷氨酸缓冲液中测试,而细胞色素c在磷酸钠溶液(Na_2PO_4)中测试。飞秒TAS用波长在418 nm \ r \ n处的泵浦脉冲和光谱在440和760 nm之间的超连续谱探针进行。用635nm连续波光源以1.6mW / cm 2的强度进行0.5小时的红光照射。我们发现还原和氧化的细胞色素c的瞬态和动力学衰减\ r \ nrates与以前的文献一致。但是,在当前的TAS测试参数下,我们找不到线粒体的任何瞬态,并且我们希望这可能是由于低信噪比或泵浦波长的选择。

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  • 来源
    《Mechanisms of Photobiomodulation Therapy XIV》|2019年|108610E.1-108610E.10|共10页
  • 会议地点 1605-7422;2410-9045
  • 作者单位

    Department of Physics and Astronomy, Texas AM University, College Station, TX 77843 sean_oconnor@tamu.edu;

    Department of Biomedical Engineering, Texas AM University, College Station, TX 77843;

    Engility Corporation, JBSA Fort Sam Houston, TX 78234;

    Engility Corporation, JBSA Fort Sam Houston, TX 78234;

    National Research Council, Airman Systems Directorate, Bioeffects Division, Optical RadiationBioeffects Branch, JBSA Fort Sam Houston, TX 78234 Air Force Research Lab, Airman Systems Directorate, Bioeffects Division, Optical RadiationBioeffects Branch, JBSA Fort Sam Houston, TX 78234;

    Air Force Research Lab, Airman Systems Directorate, Bioeffects Division, Optical RadiationBioeffects Branch, JBSA Fort Sam Houston, TX 78234;

    Department of Physics and Astronomy, Texas AM University, College Station, TX 77843 Department of Physics, Baylor University, Waco, TX 76798;

    Department of Physics and Astronomy, Texas AM University, College Station, TX 77843 Department of Biomedical Engineering, Texas AM University, College Station, TX 77843;

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