Abstract

The advent of ultrafast X-ray free-electron lasers (XFELs) opens the tantalizing possibility of the atomic-resolution imaging of reproducible objects such as viruses, nanoparticles, single molecules, clusters, and perhaps biological cells, achieving a resolution for single particle imaging better than a few tens of nanometers. Improving upon this is a significant challenge which has been the focus of a global single particle imaging (SPI) initiative launched in December 2014 at the Linac Coherent Light Source (LCLS), SLAC National Accelerator Laboratory, USA. A roadmap was outlined, and significant multi-disciplinary effort has since been devoted to work on the technical challenges of SPI such as radiation damage, beam characterization, beamline instrumentation and optics, sample preparation and delivery and algorithm development at multiple institutions involved in the SPI initiative. Currently, the SPI initiative has achieved 3D imaging of rice dwarf virus (RDV) and coliphage PR772 viruses at ~10 nm resolution by using soft X-ray FEL pulses at the Atomic Molecular and Optical (AMO) instrument of LCLS. Meanwhile, diffraction patterns with signal above noise up to the corner of the detector with a resolution of ~6 Ångström (Å) were also recorded with hard X-rays at the Coherent X-ray Imaging (CXI) instrument, also at LCLS. Achieving atomic resolution is truly a grand challenge and there is still a long way to go in light of recent developments in electron microscopy. However, the potential for studying dynamics at physiological conditions and capturing ultrafast biological, chemical and physical processes represents a tremendous potential application, attracting continued interest in pursuing further method development. In this paper, we give a brief introduction of SPI developments and look ahead to further method development.

Highlights

  • The advent of ultrafast X-ray free-electron lasers (XFELs) opens the tantalizing possibility of the atomic-resolution imaging of reproducible objects such as viruses, nanoparticles, single molecules, clusters, and perhaps biological cells, achieving a resolution for single particle imaging better than a few tens of nanometers

  • Special diagnostics required for the experiment, such as the ion/e− TOF, high speed camera, fluorescence detector and pumping laser system and the space they require should be taken into consideration

  • Finding, background subtraction detector large calibrations the XFELadvanced focus and the patterns areHit collected by the detector

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Summary

Coherent Diffraction Imaging Using Synchrotron Light Source

High-resolution structure determination of macromolecular and biological particles is an important tool for the life science and biological community [1,2,3,4]. Fifty of them [24,31,32,38,42,43,44,45,46,47,48,49,50,51,52,53,54,55,56,57,58,59,60,61,62,63,64,65,66,67,68,69,70,71,72,73,74,75,76,77,78,79,80,81,82,83,84,85,86,87] were selected to generate the word cloud of Figure 1 which shows that reconstruction, diffraction, sample, resolution, structure and coherent are the most used terms during the last 18 years of synchrotron-based CDI papers. Looking forward, the investment X-ray facilities are putting into DLSR operations will yield

Coherent
The Road Map
Setup and the Experiment Procedure
Current Status
Schematic of a single-particleimaging imaging measurement using femtosecond
Lightand
(Figures were reproduced from
Sample Selection
Detector and Data Analysis
Diffusion
Summary
Findings
Methods
Full Text
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