Titlebook: Biophysical Techniques in Photosynthesis; Volume II Thijs J. Aartsma,J?rg Matysik Book 2008 Springer Science+Business Media B.V. 2008 Prote

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https://doi.org/10.1007/978-3-662-08273-7tential of unlocking many novel details of cytoplasmic order and macromolecular structure with nanometer resolution. Interfacing this plethora of structural information with genomic and physiological data holds the promise of unprecedented advancement in biology and medicine. Three-dimensional elect

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Ulf Lubienetzki,Heidrun Schüler-Lubienetzkitures of these complexes are indispensable for a better understanding of the underlying molecular mechanism of light reactions. The key step in the structure determination of these complexes by X-ray crystallography is crystallization. Here we review the major aspects concerning membrane protein cry

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https://doi.org/10.1007/978-3-662-61829-5llization and X-ray structure analysis of the large photosynthetic protein complexes are discussed. In the second part of the chapter, selected structures of the protein complexes are presented and the function of the proteins is briefly discussed based on the structural information.

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,50?Years of Lassa Fever Research, molecules. Electron crystallography of two-dimensional crystals has become a powerful alternative to X-ray crystallography and NMR spectroscopy for the determination of the structure of proteins or protein complexes. The electron crystallography approach is particularly suitable for the study of me

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Arnold Mendelssohn an Lassalle,emonstration and validation of new methods using simple dilute dye solutions, many applications of these new techniques have been to photosynthetic systems. The reasons for this are not hard to find: photosynthetic pigment protein complexes function through a delicate interplay of interpigment and p

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https://doi.org/10.1007/978-88-470-0511-2le as an image with time and wavelength along the axes. The instrument response width is about 1% of the time range (of typically 200 ps to 2 ns). The spectral window of 250 nm may lie between 250 and 850 nm. Such spectrotemporal measurements using low excitation intensities have become routine. Sop