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• W4385743567 abstract "For a comprehensive understanding, the structure and function of molecules and molecular complexes should be investigated in their operational environment. To this end, many efforts have been made to develop in-situ biological spectroscopy. In the late 1970s, the intact enveloped virus PM2 was studied by 31P wide-line NMR, because of its simplicity, lipid envelope, and high yield, and it was possible to obtain in-situ information about the membrane and infectivity. The dynamic structures of the chromosomes were then analysed by 31P cross-polarisation NMR. Once the high-resolution solid-state NMR was established, cell walls and cell components were extensively investigated in situ using specific isotope-labelling. Dynamic nuclear polarisation (DNP) was also used to increase sensitivity. The intact structure of a light-harvesting device, the chlorosome, could be determined by uniform 13C-labelling and the proton-driven spin-diffusion caused by 13C–13C dipolar interactions, because the basic unit, bacteriochlorophyll c, was relatively small. Currently, in-situ analysis of photo-intermediates of a photoreceptor protein has been carried out using photo-illumination, cryo-trapping and DNP. Thermodynamic parameters regulating the energy transduction at the Foa–c subunit interface have been estimated from the structure analysis of a biological molecular motor, FoF1ATP synthase, using specific SAIL-labelling and in-situ CP/MAS-NMR." @default.
• W4385743567 created "2023-08-11" @default.
• W4385743567 creator A5088721614 @default.
• W4385743567 date "2023-01-01" @default.
• W4385743567 modified "2023-09-26" @default.
• W4385743567 title "In-situ solid-state nuclear magnetic resonance spectroscopy of intact biological systems" @default.
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• W4385743567 doi "https://doi.org/10.1016/bs.arnmr.2023.07.001" @default.
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