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      Sub-millisecond time-resolved SAXS using a continuous-flow mixer and X-ray microbeam

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          Abstract

          The development of a high-duty-cycle microsecond time-resolution SAXS capability at the Biophysics Collaborative Access Team beamline (BioCAT) 18ID at the Advanced Photon Source, Argonne National Laboratory, USA, is reported.

          Abstract

          Small-angle X-ray scattering (SAXS) is a well established technique to probe the nanoscale structure and interactions in soft matter. It allows one to study the structure of native particles in near physiological environments and to analyze structural changes in response to variations in external conditions. The combination of microfluidics and SAXS provides a powerful tool to investigate dynamic processes on a molecular level with sub-millisecond time resolution. Reaction kinetics in the sub-millisecond time range has been achieved using continuous-flow mixers manufactured using micromachining techniques. The time resolution of these devices has previously been limited, in part, by the X-ray beam sizes delivered by typical SAXS beamlines. These limitations can be overcome using optics to focus X-rays to the micrometer size range providing that beam divergence and photon flux suitable for performing SAXS experiments can be maintained. Such micro-SAXS in combination with microfluidic devices would be an attractive probe for time-resolved studies. Here, the development of a high-duty-cycle scanning microsecond-time-resolution SAXS capability, built around the Kirkpatrick–Baez mirror-based microbeam system at the Biophysics Collaborative Access Team (BioCAT) beamline 18ID at the Advanced Photon Source, Argonne National Laboratory, is reported. A detailed description of the microbeam small-angle-scattering instrument, the turbulent flow mixer, as well as the data acquisition and control and analysis software is provided. Results are presented where this apparatus was used to study the folding of cytochrome  c. Future prospects for this technique are discussed.

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          Author and article information

          Journal
          J Synchrotron Radiat
          J Synchrotron Radiat
          J. Synchrotron Rad.
          Journal of Synchrotron Radiation
          International Union of Crystallography
          0909-0495
          1600-5775
          01 November 2013
          01 October 2013
          01 October 2013
          : 20
          : Pt 6 ( publisher-idID: s130600 )
          : 820-825
          Affiliations
          [a ]BioCAT, CSRRI and Department BCS, Illinois Institute of Technology , 3101 South Dearborn, Chicago, IL 60616, USA
          [b ]Department of Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School , 364 Plantation Street, LRB 919, Worcester, MA 01605, USA
          Author notes
          Correspondence e-mail: rita.graceffa@ 123456gmail.com
          [‡]

          Present address: Institute for X-ray Physics, Georg-August-Universität Göttingen, Friedrich-Hund-Platz 1, 37077 Göttingen, Germany.

          [§]

          Present address: Department of Physics, DePaul University, 2219 North Kenmore Avenue, Chicago, IL 60614, USA.

          Article
          ys5080 JSYRES S0909049513021833
          10.1107/S0909049513021833
          3795536
          24121320
          6848c9cb-e729-491f-9d58-533f637292bc
          © Rita Graceffa et al. 2013

          This is an open-access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.

          History
          : 30 May 2013
          : 05 August 2013
          Categories
          Diffraction Structural Biology

          Radiology & Imaging
          micro-saxs,time-resolved,protein folding
          Radiology & Imaging
          micro-saxs, time-resolved, protein folding

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