Abstract

X-ray free-electron lasers generate intense femtosecond X-ray pulses, so that high-resolution structure determination becomes feasible from noncrystalline samples, such as single particles or single molecules. At the moment, the orientation of sample particles cannot be precisely controlled, and consequently the unknown orientation needs to be recovered using computational algorithms. This delays the model reconstruction until all the scattering patterns have been re-oriented, which often entails a long elapse of time and until the completion of the experiment. The scattering patterns from single particles or multiple particles can be summed to form a virtual powder diffraction pattern, and the low-resolution region, corresponding to the small-angle X-ray scattering (SAXS) regime, can be analysed using existing SAXS methods. This work presents a pipeline that converts single-particle data sets into SAXS data, from which real-time model reconstruction is achieved using the model retrieval approach implemented in the software package SASTBX [Liu, Hexemer & Zwart (2012). J. Appl. Cryst.45, 587-593]. To illustrate the applications, two case studies are presented with real experimental data sets collected at the Linac Coherent Light Source.

Highlights

  • One of the ultimate goals for the structural biology community is to study molecular structure and dynamics using single molecules as samples

  • The signals are spherically averaged, yielding a one-dimensional scattering profile that contains structural information. This is the so-called small/wide-angle X-ray scattering (SAXS/ WAXS) method, which is a powerful technique for studying molecular structure and dynamics in solution (Datta et al, 2009; Hura et al, 2009; Putnam et al, 2007; Nishimura et al, 2009)

  • 666 Ma and Liu Model reconstruction for single-particle scattering using small-angle X-ray scattering (SAXS) methods back detector measures the desired data, which are the focus for the analysis presented here

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Summary

Introduction

One of the ultimate goals for the structural biology community is to study molecular structure and dynamics using single molecules as samples. Heretofore X-rays have been widely applied in structure determinations of matter at microscopic scales. Because of the radiation damage induced by X-rays, the dosage has to be limited to ensure that the sample is not destroyed during measurement. The signals are spherically averaged, yielding a one-dimensional scattering profile that contains structural information. This is the so-called small/wide-angle X-ray scattering (SAXS/ WAXS) method, which is a powerful technique for studying molecular structure and dynamics in solution (Datta et al, 2009; Hura et al, 2009; Putnam et al, 2007; Nishimura et al, 2009)

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