Possible Pathway for Ubiquinone Shuttling in Rhodospirillum rubrum Revealed by Molecular Dynamics Simulation

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Pubblicato in:Biophysical Journal vol. 92, no. 1 (Jan 1, 2007), p. 23-33
Autore principale: Aird, A
Altri autori: Wrachtrup, J, Schulten, K, Tietz, C
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Biophysical Society
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100 1 |a Aird, A 
245 1 |a Possible Pathway for Ubiquinone Shuttling in Rhodospirillum rubrum Revealed by Molecular Dynamics Simulation 
260 |b Biophysical Society  |c Jan 1, 2007 
513 |a Journal Article 
520 3 |a In the last decade, the structures of many components of the photosynthetic apparatus of purple bacteria, as well as the mutual organization of these components within the purple membrane, were resolved. One key question that emerged concerned the assembly of the core complex consisting of the reaction center (RC) and the light-harvesting 1 (LH1) complex. In some species, like Rhodobacter sphaeroides, the ring-shaped LH1 complex was found to be open, whereas other species, like Rhodospirillum rubrum, have a closed ring surrounding the reaction center. This poses the question of how the ubiquinone molecule that transports electrons and protons from the RC to the cytochrome bc^sub 1^ complex overcomes the apparent barrier of the LH1 ring. In this study, we investigated how, in the case of a closed LH1 ring, the ubiquinone molecule diffuses through the LH1 ring. For this purpose, the LH1 structure of R. rubrum was modeled and the potential of mean force along the diffusion pathway through the LH1 was determined by steered molecular-dynamics simulations. The potential was reconstructed using the fluctuation theorem in combination with the stiff spring approximation. An upper limit for the mean first-passage time for diffusion of ubiquinone through the LH1 ring, based on a worst-case scenario potential, was calculated as ~8 × 10^sup -3^ s, which is still in agreement with known turnover rates of RC and RC-LH1 complexes in the range of ~1000 Hz. [PUBLICATION ABSTRACT]   In the last decade, the structures of many components of the photosynthetic apparatus of purple bacteria, as well as the mutual organization of these components within the purple membrane, were resolved. One key question that emerged concerned the assembly of the core complex consisting of the reaction center (RC) and the light-harvesting 1 (LH1) complex. In some species, like Rhodobacter sphaeroides, the ring-shaped LH1 complex was found to be open, whereas other species, like Rhodospirillum rubrum, have a closed ring surrounding the reaction center. This poses the question of how the ubiquinone molecule that transports electrons and protons from the RC to the cytochrome bc(1) complex overcomes the apparent barrier of the LH1 ring. In this study, we investigated how, in the case of a closed LH1 ring, the ubiquinone molecule diffuses through the LH1 ring. For this purpose, the LH1 structure of R. rubrum was modeled and the potential of mean force along the diffusion pathway through the LH1 was determined by steered molecular-dynamics simulations. The potential was reconstructed using the fluctuation theorem in combination with the stiff spring approximation. An upper limit for the mean first-passage time for diffusion of ubiquinone through the LH1 ring, based on a worst-case scenario potential, was calculated as approximately 8 x 10(-3) s, which is still in agreement with known turnover rates of RC and RC-LH1 complexes in the range of approximately 1000 Hz. 
650 2 2 |a Biological Transport 
650 2 2 |a Computer Simulation 
650 2 2 |a Electrons 
650 2 2 |a Light-Harvesting Protein Complexes 
650 2 2 |a Lipid Bilayers  |x chemistry 
650 2 2 |a Models, Chemical 
650 2 2 |a Models, Molecular 
650 2 2 |a Models, Statistical 
650 2 2 |a Molecular Conformation 
650 2 2 |a Phosphatidylcholines  |x chemistry 
650 2 2 |a Protein Conformation 
650 2 2 |a Protons 
650 1 2 |a Rhodospirillum rubrum  |x metabolism 
650 1 2 |a Ubiquinone  |x chemistry 
653 |a Bacteria 
653 |a Molecular biology 
653 |a Simulation 
653 |a Membranes 
653 |a Molecules 
653 |a Diffusion 
653 |a Environmental 
700 1 |a Wrachtrup, J 
700 1 |a Schulten, K 
700 1 |a Tietz, C 
773 0 |t Biophysical Journal  |g vol. 92, no. 1 (Jan 1, 2007), p. 23-33 
786 0 |d ProQuest  |t Science Database 
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