Literature DB >> 12080129

Spectroscopy of single phycoerythrocyanin monomers: dark state identification and observation of energy transfer heterogeneities.

P Zehetmayer1, Th Hellerer, A Parbel, H Scheer, A Zumbusch.   

Abstract

Phycoerythrocyanin (PEC) is part of the light harvesting system of cyanobacteria. The PEC monomer contains one phycoviolobilin chromophore, which transfers excitation energy onto two phycocyanobilin chromophores. Many spectroscopical methods have been used in the past to study the bulk properties of PEC. These methods average over many molecules. Therefore, differences in the behavior of individual molecules remain hidden. The energy transfer within photosynthetic complexes is however sensitive to changes in the spectroscopic properties of the participating subunits. Knowledge about heterogeneities is therefore important for the description of the energy transfer in photosynthetic systems. Here, the recording of the fluorescence emission of single PEC molecules is used as a tool to obtain such information. Spectrally resolved detection as well as double resonance excitation of single PEC molecules is used to investigate their bleaching behavior. The trans isomer of the phycoviolobilin chromophore is identified as a short-lived dark state of monomeric PEC. Polarization sensitive single molecule detection is used for the direct observation of the energy transfer in individual PEC molecules. The experiments reveal that more than one-half of the PEC molecules exhibit an energy transfer behavior significantly different from the bulk. These heterogeneities persist on a time scale of several seconds. Model calculations lead to the conclusion that they are caused by minor shifts in the spectra of the chromophores.

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Year:  2002        PMID: 12080129      PMCID: PMC1302156          DOI: 10.1016/S0006-3495(02)75178-3

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  10 in total

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4.  Real-time light-driven dynamics of the fluorescence emission in single green fluorescent protein molecules.

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7.  Refined three-dimensional structure of phycoerythrocyanin from the cyanobacterium Mastigocladus laminosus at 2.7 A.

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8.  Myosin conformational states determined by single fluorophore polarization.

Authors:  D M Warshaw; E Hayes; D Gaffney; A M Lauzon; J Wu; G Kennedy; K Trybus; S Lowey; C Berger
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9.  Three-stepped rotation of subunits gamma and epsilon in single molecules of F-ATPase as revealed by polarized, confocal fluorometry.

Authors:  K Häsler; S Engelbrecht; W Junge
Journal:  FEBS Lett       Date:  1998-04-24       Impact factor: 4.124

10.  Carbocyanine dye orientation in red cell membrane studied by microscopic fluorescence polarization.

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Journal:  Biophys J       Date:  1979-06       Impact factor: 4.033

  10 in total
  4 in total

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3.  FRAP analysis on red alga reveals the fluorescence recovery is ascribed to intrinsic photoprocesses of phycobilisomes than large-scale diffusion.

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4.  Light-induced energetic decoupling as a mechanism for phycobilisome-related energy dissipation in red algae: a single molecule study.

Authors:  Lu-Ning Liu; Abdalmohsen T Elmalk; Thijs J Aartsma; Jean-Claude Thomas; Gerda E M Lamers; Bai-Cheng Zhou; Yu-Zhong Zhang
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  4 in total

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