期刊
BIOPHYSICAL JOURNAL
卷 106, 期 9, 页码 2008-2016出版社
CELL PRESS
DOI: 10.1016/j.bpj.2014.03.023
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资金
- Deutsche Forschungsgemeinschaft [KO 1359/16-1, GZ: 436 EST 113/4/0-1, GRK1640]
- Estonian Research Council [IUT02-28]
- BBSRC
- BBSRC [BB/G003831/1] Funding Source: UKRI
- Biotechnology and Biological Sciences Research Council [BB/G003831/1] Funding Source: researchfish
We have recorded fluorescence-excitation and emission spectra from single LH2 complexes from Rhodopseudomonas (Rps.) acidophila. Both types of spectra show strong temporal spectral fluctuations that can be visualized as spectral diffusion plots. Comparison of the excitation and emission spectra reveals that for most of the complexes the lowest exciton transition is not observable in the excitation spectra due to the cutoff of the detection filter characteristics. However, from the spectral diffusion plots we have the full spectral and temporal information at hand and can select those complexes for which the excitation spectra are complete. Correlating the red most spectral feature of the excitation spectrum with the blue most spectral feature of the emission spectrum allows an unambiguous assignment of the lowest exciton state. Hence, application of fluorescence-excitation and emission spectroscopy on the same individual LH2 complex allows us to decipher spectral subtleties that are usually hidden in traditional ensemble spectroscopy.
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