Evidence map›Paper›PMID 24806933›Full record

ArticleBiophysical journal2014

Single-molecule spectroscopy unmasks the lowest exciton state of the B850 assembly in LH2 from Rps. acidophila.

Ralf Kunz, Kõu Timpmann, June Southall, Richard J Cogdell, Arvi Freiberg, Jürgen Köhler

Abstract read
In one paragraph

Article in Biophysical journal, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors.

Ralf KunzExperimental Physics IV and Bayreuth Institute for Macromolecular Research (BIMF), University of Bayreuth, Bayreuth, Germany.
Kõu TimpmannInstitute of Physics, University of Tartu, Tartu, Estonia.
June SouthallInstitute of Molecular, Cell and Systems Biology, College of Medical Veterinary and Life Sciences, Biomedical Research Building, University of Glasgow, Glasgow, Scotland, United Kingdom.
Richard J CogdellInstitute of Molecular, Cell and Systems Biology, College of Medical Veterinary and Life Sciences, Biomedical Research Building, University of Glasgow, Glasgow, Scotland, United Kingdom.
Arvi FreibergInstitute of Physics, University of Tartu, Tartu, Estonia; Institute of Molecular and Cell Biology, University of Tartu, Tartu, Estonia.
Jürgen KöhlerExperimental Physics IV and Bayreuth Institute for Macromolecular Research (BIMF), University of Bayreuth, Bayreuth, Germany. Electronic address: juergen.koehler@uni-bayreuth.de.

Funding

Biotechnology and Biological Sciences Research Council BB/G003831/1
6 · The paper itself

Abstract

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.

Indexed as

DiffusionLight-Harvesting Protein ComplexesRhodopseudomonasSpectrometry, FluorescenceLight-Harvesting Protein Complexes

Identifiers

PMID24806933
PMCPMC4017283

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