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Determination of Crystal Structures01:29

Determination of Crystal Structures

124
In the late 1800s, the revelation that light extended beyond visible wavelengths led to the discovery of X-rays by Wilhelm Roentgen. Recognized as high-energy electromagnetic radiation with short wavelengths, X-rays prompted exploration into their interaction with crystals. Max von Laue proposed in 1912 that the periodic arrangement of atoms, ions, or molecules in crystals would cause them to diffract X-rays, a hypothesis confirmed through experiments with copper sulfate and zinc sulfide...
124
X-ray Crystallography02:18

X-ray Crystallography

27.2K
The size of the unit cell and the arrangement of atoms in a crystal may be determined from measurements of the diffraction of X-rays by the crystal, termed X-ray crystallography.
Diffraction
Diffraction is the change in the direction of travel experienced by an electromagnetic wave when it encounters a physical barrier whose dimensions are comparable to those of the wavelength of the light. X-rays are electromagnetic radiation with wavelengths about as long as the distance between neighboring...
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X-ray Diffraction of Biological Samples01:10

X-ray Diffraction of Biological Samples

5.2K
X-ray diffraction or XRD is an analytical tool that utilizes X-rays to study ordered structures such as crystalline organic and inorganic samples, polycrystalline materials, proteins, carbohydrates, and drugs.
According to Bragg's law, when X-rays strike the sample positioned on a stage, the rays are  scattered by the electron clouds around the sample atoms. The  X-ray diffraction or scattering is caused by constructive interference of the X-ray waves that reflect off the internal...
5.2K
Crystallographic Point Groups01:29

Crystallographic Point Groups

109
Crystallographic point groups represent the various symmetry operations that can occur within crystals. They are unique in that at least one point will always remain unchanged during these actions. For instance, consider the triclinic system. This system, devoid of any axis or plane of symmetry, aligns with the C1 and Ci point groups.where Cᵢ is characterized solely by a center of inversion.Contrastingly, the monoclinic system introduces an element of symmetry. This system with one plane...
109

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Updated: Apr 18, 2026

Microcrystallography of Protein Crystals and In Cellulo Diffraction
09:35

Microcrystallography of Protein Crystals and In Cellulo Diffraction

Published on: July 21, 2017

9.7K

Serial crystallography for the masses?

Jonathan P Wright1

  • 1ESRF , 71 Avenue des Martyrs, Grenoble, 38000, France.

Iucrj
|January 23, 2015
PubMed
Summary
This summary is machine-generated.

Serial crystallography is now feasible with more radiation sources. Researchers can recover crystallographic intensities from sparse, randomly oriented frames, expanding experimental possibilities.

Keywords:
EMC algorithmreconstruction of diffraction intensityserial crystallographysparse data

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Area of Science:

  • Crystallography
  • Structural Biology
  • Materials Science

Background:

  • Serial crystallography typically requires high-intensity, focused X-ray beams for successful data collection.
  • Indexing diffraction patterns from randomly oriented microcrystals is a significant challenge in serial crystallography.

Purpose of the Study:

  • To demonstrate that crystallographic intensities can be recovered from sparse diffraction data.
  • To expand the applicability of serial crystallography to a wider range of radiation sources.

Main Methods:

  • Utilizing computational methods to process diffraction frames from randomly oriented microcrystals.
  • Developing algorithms capable of extracting intensity information from frames that are too sparse for traditional indexing.

Main Results:

  • Crystallographic intensities were successfully recovered from sparse, randomly oriented diffraction frames.
  • The findings suggest that serial crystallography is viable with less intense or more divergent radiation sources.

Conclusions:

  • The study broadens the scope of accessible radiation sources for serial crystallography.
  • This advancement facilitates structural determination for a wider array of samples and experimental setups.