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  X-ray damage to the Mn4Ca complex in single crystals of photosystem II: A case study for metalloprotein crystallography

Yano, J., Kern, J., Irrgang, K., Latimer, M. J., Bergmann, U., Glatzel, P., et al. (2005). X-ray damage to the Mn4Ca complex in single crystals of photosystem II: A case study for metalloprotein crystallography. Proceedings of the National Academy of Sciences of the USA, 102(34), 12047-12052. doi:10.1073/pnas.0505207102.

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 Urheber:
Yano, Junko, Autor
Kern, Jana1, 2, Autor           
Irrgang, Klaus−Dieter, Autor
Latimer, Matthew J., Autor
Bergmann, Uwe, Autor
Glatzel, Pieter, Autor
Pushkar, Yulia N., Autor
Biesiadka, Jacek, Autor
Loll, Bernhard3, Autor           
Sauer, Kenneth, Autor
Messinger, Johannes, Autor
Zouni, Athina, Autor
Yachandra, Vittal K., Autor
Affiliations:
1Structure of neocortical circuits, Max Planck Institute for Medical Research, Max Planck Society, ou_1497742              
2Department of Biomedical Optics, Max Planck Institute for Medical Research, Max Planck Society, ou_1497699              
3Department of Biomolecular Mechanisms, Max Planck Institute for Medical Research, Max Planck Society, ou_1497700              

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Schlagwörter: manganese, oxygen evolution, water oxidation, x-ray spectroscopy
 Zusammenfassung: X-ray absorption spectroscopy was used to measure the damage caused by exposure to x-rays to the Mn(4)Ca active site in single crystals of photosystem II as a function of dose and energy of x-rays, temperature, and time. These studies reveal that the conditions used for structure determination by x-ray crystallography cause serious damage specifically to the metal-site structure. The x-ray absorption spectra show that the structure changes from one that is characteristic of a high-valent Mn(4)(III(2),IV(2)) oxo-bridged Mn(4)Ca cluster to that of Mn(II) in aqueous solution. This damage to the metal site occurs at a dose that is more than one order of magnitude lower than the dose that results in loss of diffractivity and is commonly considered safe for protein crystallography. These results establish quantitative x-ray dose parameters that are applicable to redox-active metalloproteins. This case study shows that a careful evaluation of the structural intactness of the active site(s) by spectroscopic techniques can validate structures derived from crystallography and that it can be a valuable complementary method before structure-function correlations of metalloproteins can be made on the basis of high-resolution x-ray crystal structures.

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Sprache(n): eng - English
 Datum: 2005-04-242005-08-23
 Publikationsstatus: Erschienen
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 Art der Begutachtung: Expertenbegutachtung
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Titel: Proceedings of the National Academy of Sciences of the USA
  Alternativer Titel : PNAS
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: 102 (34) Artikelnummer: - Start- / Endseite: 12047 - 12052 Identifikator: -