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Addressing high excitation conditions in time-resolved X-ray diffraction experiments and issues of biological relevance
Institution:1. Department of Biochemistry, University of Toronto, 1 King''s College Circle, Toronto, ON, M5S 1A8, Canada;2. Departments of Chemistry and Physics, University of Toronto, 80 St. George Street, Toronto, Ontario, M5S 3H6, Canada;1. Institut für Medizinische Physik und Biophysik (CC2), Charité, and, Zentrum für Biophysik und Bioinformatik, Humboldt-Unversität zu Berlin, Berlin, 10117, Germany;2. Eccles Institute of Neuroscience, John Curtin School of Medical Research, The Australian National University, Canberra, ACT 2600, Australia;1. Department of Structural and Molecular Biology, University College London, London, United Kingdom;2. Department of Applied Physics, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, Bangi, Malaysia;1. Center for Computational Mathematics, Flatiron Institute, 162 5th Ave, New York, NY, 10010, United States;2. Center for Computational Biology, Flatiron Institute, 162 5th Ave, New York, NY, 10010, United States;3. Department of Computer Science, Princeton University, 35 Olden St, Princeton, NJ, 08544, United States
Abstract:One of the most important fundamental questions connecting chemistry to biology is how chemistry scales in complexity up to biological systems where there are innumerable possible pathways and competing processes. With the development of ultrabright electron and x-ray sources, it has been possible to literally light up atomic motions to directly observe the reduction in dimensionality in the barrier crossing region to a few key reaction modes. How do these chemical processes further couple to the surrounding protein or macromolecular assembly to drive biological functions? Optical methods to trigger photoactive biological processes are needed to probe this issue on the relevant timescales. However, the excitation conditions have been in the highly nonlinear regime, which questions the biological relevance of the observed structural dynamics.
Keywords:Time-resolved crystallography  Structure–function relationships  Laser illumination guidelines
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