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Related Concept Videos

Molecular Shapes01:18

Molecular Shapes

Molecules have characteristic shapes that are crucial for their function. The arrangement of various electron groups around the central atom dictates their molecular geometry. Electron pairs in the valence shell of a central atom will adopt an arrangement that minimizes repulsions between the electron pairs by maximizing the distance between them. The valence electrons form either bonding pairs, located primarily between bonded atoms, or lone pairs.
Two regions of electron density in a diatomic...
Positive Regulator Molecules01:45

Positive Regulator Molecules

To consistently produce healthy cells, the cell cycle—the process that generates daughter cells—must be precisely regulated.
Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Ions, Molecules, and Compounds01:23

Ions, Molecules, and Compounds

Ions - When an atom participates in a chemical reaction that results in the donation or acceptance of one or more electrons, the atom becomes positively or negatively charged. This frequently happens for most atoms to have a full valence shell. This can happen either by gaining electrons to fill a shell that is more than half-full or by giving away electrons to empty a shell that is less than half-full, thereby leaving the next smaller electron shell as the new, full valence shell. An atom with...
Negative Regulator Molecules01:23

Negative Regulator Molecules

Positive regulators allow a cell to advance through cell cycle checkpoints. Negative regulators have an equally important role as they terminate a cell’s progression through the cell cycle—or pause it—until the cell meets specific criteria.
Molecules and Compounds02:38

Molecules and Compounds

Atoms and Molecules

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Related Experiment Video

Updated: May 8, 2026

Spatiotemporally Controlled Nuclear Translocation of Guests in Living Cells Using Caged Molecular Glues as Photoactivatable Tags
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Spatiotemporally Controlled Nuclear Translocation of Guests in Living Cells Using Caged Molecular Glues as Photoactivatable Tags

Published on: January 17, 2019

Putting molecules in their place.

Bertrand P Cinquin1, Myan Do, Gerry McDermott

  • 1Department of Anatomy, University of California San Francisco, San Francisco, California.

Journal of Cellular Biochemistry
|August 23, 2013
PubMed
Summary
This summary is machine-generated.

Correlative imaging combines cryogenic fluorescence tomography (CFT) with soft X-ray tomography (SXT) for detailed 3D cell analysis. This approach integrates molecular localization with high-resolution cell structure imaging in a near-native state.

Keywords:
CORRELATED IMAGINGFLUORESCENCEMICROSCOPYSOFT X-RAYTOMOGRAPHY

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Spatiotemporally Controlled Nuclear Translocation of Guests in Living Cells Using Caged Molecular Glues as Photoactivatable Tags
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Published on: July 12, 2016

Area of Science:

  • Cell Biology
  • Microscopy
  • Biophysics

Background:

  • Individual microscopy techniques have limitations in capturing comprehensive cell structure and molecular organization.
  • Correlative imaging, combining data from multiple microscopes, offers a solution to overcome these limitations.
  • Emerging microscope technologies are advancing the field of correlative imaging.

Purpose of the Study:

  • To describe the correlation of cryogenic fluorescence tomography (CFT) with soft X-ray tomography (SXT).
  • To integrate 3D molecular localization data with high-resolution 3D cell reconstruction.
  • To present the current state and future outlook of correlative CFT-SXT.

Main Methods:

  • Imaging cells using cryogenic fluorescence tomography (CFT) for 3D molecular localization.
  • Imaging the same cells using soft X-ray tomography (SXT) for high-resolution 3D reconstruction.
  • Correlating data from both CFT and SXT modalities.
  • Imaging specimens in a near-native, cryopreserved state.

Main Results:

  • Successful integration of 3D molecular localization data (CFT) with high-resolution 3D cell reconstruction (SXT).
  • Demonstration of correlative cryogenic fluorescence tomography-soft X-ray tomography (CFT-SXT) for comprehensive cellular analysis.
  • Imaging cells in a cryopreserved state preserves native structure and molecular information.

Conclusions:

  • Correlative CFT-SXT provides a powerful method for detailed 3D cellular and molecular analysis.
  • This integrated approach overcomes the limitations of individual microscopy techniques.
  • The described method represents the current state of the art and offers promising future applications in cell biology research.