[NMR paper] Analysis of the electronic structure of the Special Pair of a Bacterial Photosynthetic Reaction Center by (13) C Photochemically Induced Dynamic Nuclear Polarization Magic-Angle Spinning NMR Using a Double-Quantum Axis.
Analysis of the electronic structure of the Special Pair of a Bacterial Photosynthetic Reaction Center by (13) C Photochemically Induced Dynamic Nuclear Polarization Magic-Angle Spinning NMR Using a Double-Quantum Axis.
Related ArticlesAnalysis of the electronic structure of the Special Pair of a Bacterial Photosynthetic Reaction Center by (13) C Photochemically Induced Dynamic Nuclear Polarization Magic-Angle Spinning NMR Using a Double-Quantum Axis.
Photochem Photobiol. 2017 Jul 26;:
Authors: Najdanova M, Gräsing D, Alia A, Matysik J
Abstract
The origin of the functional symmetry break in bacterial photosynthesis challenges since several decades. Although structurally very similar, the two branches of cofactors in the reaction center (RC) protein complex act very differently. Upon photochemical excitation, an electron is transported along one branch, while the other remains inactive. Photochemically induced dynamic nuclear polarization (photo-CIDNP) magic-angle spinning (MAS) (13) C NMR revealed that the two bacteriochlorophyll cofactors forming the "Special Pair" donor dimer are already well distinguished in the electronic ground-state. These previous studies are relying solely on (13) C-(13) C correlation experiments as Radio-Frequency Driven Recoupling (RFDR) and dipolar-assisted rotational resonance (DARR). Obviously, the chemical shift assignment is difficult in a dimer of tetrapyrrole macrocycles, having eight pyrrole rings of similar chemical shifts. To overcome this problem, an INADEQUATE type of experiment using a POST C7 symmetry based approach is applied to selectively isotope labeled bacterial RC of Rhodobacter (R.) sphaeroides wild-type (WT). We, therefore, were able to distinguish unresolved sites of the macro-molecular dimer. The obtained chemical shift pattern is in-line with a concentric assembly of negative charge within the common center of the Special Pair super-molecule in the electronic ground-state. This article is protected by copyright. All rights reserved.
PMID: 28746728 [PubMed - as supplied by publisher]
[NMR paper] Photochemically Induced Dynamic Nuclear Polarization Observed by Solid-state NMR in a Uniformly (13)C-isotope Labeled Photosynthetic Reaction Center.
Photochemically Induced Dynamic Nuclear Polarization Observed by Solid-state NMR in a Uniformly (13)C-isotope Labeled Photosynthetic Reaction Center.
Related Articles Photochemically Induced Dynamic Nuclear Polarization Observed by Solid-state NMR in a Uniformly (13)C-isotope Labeled Photosynthetic Reaction Center.
J Phys Chem B. 2015 Jun 25;
Authors: Paul S, Bode BE, Matysik J, Alia A
Abstract
A sample of solubilized and quinone-depleted reaction centers (RC) from the purple bacterium Rhodobacter (R.) sphaeroides wild-type (WT)...
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Symmetry Break of Special Pair: Photochemically Induced Dynamic Nuclear Polarization NMR Confirms Control by Nonaromatic Substituents
Symmetry Break of Special Pair: Photochemically Induced Dynamic Nuclear Polarization NMR Confirms Control by Nonaromatic Substituents
Karthick Babu Sai Sankar Gupta, A. Alia, Huub J.M. de Groot and Jo?rg Matysik
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja402238w/aop/images/medium/ja-2013-02238w_0006.gif
Journal of the American Chemical Society
DOI: 10.1021/ja402238w
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07-03-2013 01:46 PM
[NMR paper] Symmetry break of special pair: Photochemically induced dynamic nuclear polarization NMR confirms control by nonaromatic substituents.
Symmetry break of special pair: Photochemically induced dynamic nuclear polarization NMR confirms control by nonaromatic substituents.
Symmetry break of special pair: Photochemically induced dynamic nuclear polarization NMR confirms control by nonaromatic substituents.
J Am Chem Soc. 2013 Jun 6;
Authors: Sai Sankar Gupta KB, Alia A, de Groot HJ, Matysik J
Abstract
Despite the high structural symmetry of cofactor arrangement and protein environment, light-induced electron transfer in photosynthetic reaction centers (RCs) of the purple...
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06-07-2013 10:04 AM
Intermolecular Structure Determination of Amyloid Fibrils with Magic-Angle Spinning and Dynamic Nuclear Polarization NMR
Intermolecular Structure Determination of Amyloid Fibrils with Magic-Angle Spinning and Dynamic Nuclear Polarization NMR
Marvin J. Bayro, Galia T. Debelouchina, Matthew T. Eddy, Neil R. Birkett, Catherine E. MacPhee, Melanie Rosay, Werner E. Maas, Christopher M. Dobson and Robert G. Griffin
http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jacsat/0/jacsat.ahead-of-print/ja203756x/aop/images/medium/ja-2011-03756x_0002.gif
Journal of the American Chemical Society
DOI: 10.1021/ja203756x
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08-13-2011 02:47 AM
Intermolecular structure determination of amyloid fibrils with magic-angle spinning and dynamic nuclear polarization NMR.
Intermolecular structure determination of amyloid fibrils with magic-angle spinning and dynamic nuclear polarization NMR.
Intermolecular structure determination of amyloid fibrils with magic-angle spinning and dynamic nuclear polarization NMR.
J Am Chem Soc. 2011 Jul 21;
Authors: Bayro MJ, Debelouchina GT, Eddy MT, Birkett NR, Macphee CE, Rosay MM, Maas WE, Dobson CM, Griffin RG
We describe magic-angle spinning NMR experiments designed to elucidate the interstrand architecture of amyloid fibrils. Three methods are introduced for this purpose, two...