| Literature DB >> 24466387 |
Rolf Mitzner1, Jens Rehanek2, Jan Kern3, Sheraz Gul4, Johan Hattne4, Taketo Taguchi5, Roberto Alonso-Mori6, Rosalie Tran4, Christian Weniger1, Henning Schröder7, Wilson Quevedo1, Hartawan Laksmono8, Raymond G Sierra8, Guangye Han4, Benedikt Lassalle-Kaiser4, Sergey Koroidov9, Katharina Kubicek10, Simon Schreck7, Kristjan Kunnus7, Maria Brzhezinskaya2, Alexander Firsov2, Michael P Minitti6, Joshua J Turner6, Stefan Moeller6, Nicholas K Sauter4, Michael J Bogan8, Dennis Nordlund11, William F Schlotter6, Johannes Messinger9, Andrew Borovik5, Simone Techert12, Frank M F de Groot13, Alexander Föhlisch7, Alexei Erko2, Uwe Bergmann6, Vittal K Yachandra4, Philippe Wernet1, Junko Yano4.
Abstract
L-edge spectroscopy of 3d transition metals provides important electronic structure information and has been used in many fields. However, the use of this method for studying dilute aqueous systems, such as metalloenzymes, has not been prevalent because of severe radiation damage and the lack of suitable detection systems. Here we present spectra from a dilute Mn aqueous solution using a high-transmission zone-plate spectrometer at the Linac Coherent Light Source (LCLS). The spectrometer has been optimized for discriminating the Mn L-edge signal from the overwhelming O K-edge background that arises from water and protein itself, and the ultrashort LCLS X-ray pulses can outrun X-ray induced damage. We show that the deviations of the partial-fluorescence yield-detected spectra from the true absorption can be well modeled using the state-dependence of the fluorescence yield, and discuss implications for the application of our concept to biological samples.Entities:
Keywords: Excited States; Photochemistry; Spectroscopy
Year: 2013 PMID: 24466387 PMCID: PMC3901369 DOI: 10.1021/jz401837f
Source DB: PubMed Journal: J Phys Chem Lett ISSN: 1948-7185 Impact factor: 6.475