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Related Concept Videos

Labeling DNA Probes03:31

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DNA probes are fragments of DNA labeled with a reporter tag to enable their detection or purification. The resulting labeled DNA probes can then hybridize to target nucleic acid sequences through complementary base-pairing, and may be used to recover or identify these regions.
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Immunoelectron microscopy utilizes immunogold labeling of endogenous proteins with specific antibodies to detect and localize these proteins in cells and tissues. The procedure provides insights into the distribution and quantification of protein under different stimulation conditions offering clues about their functions. Conjugating highly electron-dense gold particles with primary or secondary antibodies allow antigen detection on and within cells, with high resolution and specificity.
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Related Experiment Video

Updated: Jul 13, 2025

Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells
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Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells

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Cell-selective bioorthogonal labeling.

Wei Huang1, Scott T Laughlin1

  • 1Department of Chemistry and Institute for Chemical Biology and Drug Discovery, Stony Brook University, Stony Brook, NY 11794, USA.

Cell Chemical Biology
|October 14, 2023
PubMed
Summary
This summary is machine-generated.

Bioorthogonal chemistry enables cell-selective labeling by controlling tag incorporation, reagent localization, or reaction activation. This advances targeted biomolecule analysis in specific cell populations.

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Area of Science:

  • Biochemistry
  • Chemical Biology
  • Molecular Imaging

Background:

  • Classic bioorthogonal labeling incorporates tags into biomolecules via cellular machinery.
  • This method labels cells indiscriminately, leading to background noise in specific cell population studies.

Purpose of the Study:

  • To review advances in bioorthogonal chemistry for cell-selective labeling.
  • To highlight strategies for targeting bioorthogonal labeling to specific cell types.

Main Methods:

  • Cell-selective expression of engineered enzymes for tag incorporation.
  • Preferential localization of bioorthogonal reagents to target cells.
  • Caging bioorthogonal reagent reactivity for selective activation within specific cell populations.

Main Results:

  • Demonstrated three distinct strategies for achieving cell-selective bioorthogonal labeling.
  • Enabled targeted labeling of specific cell types, reducing non-specific background.

Conclusions:

  • Cell-selective bioorthogonal labeling overcomes limitations of traditional methods.
  • Advances in bioorthogonal chemistry facilitate precise biomolecule analysis in targeted cells.