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Volume 87, Issue 4, Pages (October 2004)

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1 Volume 87, Issue 4, Pages 2598-2608 (October 2004)
Single-Molecule Spectroscopy Selectively Probes Donor and Acceptor Chromophores in the Phycobiliprotein Allophycocyanin  Davey Loos, Mircea Cotlet, Frans De Schryver, Satoshi Habuchi, Johan Hofkens  Biophysical Journal  Volume 87, Issue 4, Pages (October 2004) DOI: /biophysj Copyright © 2004 The Biophysical Society Terms and Conditions

2 Figure 1 (A) Schematic structure of APC as it was obtained by means of x-ray crystallography. The chromophores are arranged in three pairs. (B) Chemical structure of the phycocyanobilin chromophore. The individual rings have been named from A to D. Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

3 Figure 2 (A) Transient absorption spectrum of APC in PBS as reproduced from Su-Ping et al., (B) Steady-state absorption (solid line) and fluorescence (dashed line with stars, excitation at 632nm) spectra of APC in a PBS buffer, pH 7.4. Shown in the same panel are the calculated individual absorption (solid line with open circles for α84 and solid line with stars for β84) and fluorescence spectra (dashed line with solid circles for α84 and dashed line with open stars for β84) of the chromophores in APC (see text for details). Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

4 Figure 3 Isotropic fluorescence intensity trajectories (60-ms dwell time) from single APC trimers in PVA recorded at 632-nm CW linear polarized excitation showing (A) six, (B) five, (C) four, and (D) three levels of intensity. For each panel the inset is a zoom (10-ms dwell time) of the first part of the trajectory and the graph at right represents the frequency histograms, in logarithmic scale (10-ms dwell time), of the data shown in the main panels. Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

5 Figure 4 (A and C) Time courses of the polarization degree (20 ms/bin) of single APC on 632-nm CW linear polarized excitation. (B and D) Histograms, in logarithmic scale, and Gauss fits of the polarization data from panels A and C, respectively. Also shown are the main values resulting from the fit. Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

6 Figure 5 Representative time-resolved data accounting for a single APC trimer in PVA. (A) Isotropic fluorescence intensity and (B) fluorescence lifetime trajectories. Lifetimes were estimated by MLE fitting each 1000 photons over the single-molecule fluorescence trajectory. (C) Total fluorescence decay constructed from the single-molecule fluorescence trajectory. (D) Unquenched and (E) quenched single-molecule fluorescence decays (1000 photons each) observed during the measurement of the single APC trimer. (F) Histogram of lifetimes from panel B and Gauss fits. (G) Intensity versus lifetime correlation constructed from panels A and B. Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

7 Figure 6 Overall histogram containing lifetimes estimated from decays of 1000 photons from a population of 70 single APC trimers. Also shown is a bimodal Gauss fit (lines with circles). Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

8 Figure 7 (A) Fluorescence spectral run (1s integration/spectrum) detected from a single APC trimer on 568-nm CW excitation. (B) Time course of the emission maximum of the spectra from panel A. Single-molecule fluorescence spectra accounting for (C) single β84, (D) single α84, and (E) mixture of single β84 and α84 chromophores. Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions

9 Figure 8 Photophysical scheme accounting for the processes observed in APC. D, donor; A, acceptor; RC*, radical cation; kabs, k(D)fl, k(A)fl, and kFRET are rate constants for absorption, donor fluorescence, acceptor fluorescence, and Förster energy transfer. kNR1 and kNR2 are rate constants for nonradiative deactivation. Biophysical Journal  , DOI: ( /biophysj ) Copyright © 2004 The Biophysical Society Terms and Conditions


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