Related Experiment Video
Updated: Jul 9, 2026

Visualization of miniSOG Tagged DNA Repair Proteins in Combination with Electron Spectroscopic Imaging (ESI)
Published on: September 24, 2015
Non-enzymatic covalent protein labeling using a reactive tag.
Hiroshi Nonaka1, Shinya Tsukiji, Akio Ojida
1Department of Synthetic Chemistry and Biological Chemistry, Graduate School of Engineering, Kyoto University, Katsura Campus, Nishikyo-ku, Kyoto, 615-8510, Japan.
Researchers developed a novel covalent protein labeling method using a peptide tag and molecular probe. This technique enables rapid, specific labeling of proteins, even within living cells, offering facile modification and high specificity.
Area of Science:
- Biochemistry
- Molecular Biology
- Chemical Biology
Background:
- Protein labeling is crucial for studying protein function and interactions.
- Existing methods may lack specificity or require harsh conditions.
- A need exists for efficient and specific protein labeling techniques.
Purpose of the Study:
- To introduce a new method for covalent protein labeling.
- To demonstrate the specificity and efficiency of this novel labeling technique.
- To validate the method's applicability in various conditions, including intracellular environments.
Main Methods:
- Utilizing a complementary recognition pair consisting of a peptide tag and a synthetic molecular probe.
- Achieving covalent labeling through selective molecular recognition between the tag and probe.
- Performing labeling experiments under diverse conditions, including in vitro and in cellulo.
Main Results:
- Successful rapid and specific covalent labeling of tag-fused proteins was achieved.
- The method demonstrated facile functional modification of proteins.
- High labeling specificity was observed across various experimental conditions.
- The technique proved effective for labeling proteins within living cells.
Conclusions:
- The developed method offers a robust approach for covalent protein labeling.
- Its high specificity and ease of use make it valuable for biological research.
- The ability to label proteins in situ expands its utility for cellular studies.
More Related Videos
10:36Covalent Labeling with Diethylpyrocarbonate for Studying Protein Higher-Order Structure by Mass Spectrometry
Published on: June 15, 2021
14:02Optimizing the Genetic Incorporation of Chemical Probes into GPCRs for Photo-crosslinking Mapping and Bioorthogonal Chemistry in Live Mammalian Cells
Published on: April 9, 2018
Related Concept Videos
Tagging and Fusion Proteins
Labeling DNA Probes
Radioisotopes, fluorophores, or small molecule binding partners like biotin or digoxigenin, are the most widely used reporter tags for labeling DNA probes. These labels can be attached to the probe DNA molecule via...
Immunogold Electron Microscopy
Covalently Linked Protein Regulators
These groups modify specific amino acids in a protein.
Covalently Linked Protein Regulators
These groups modify specific amino acids in a protein.
Protein Dynamics in Living Cells
Fluorescent recovery after photobleaching (FRAP) is a fluorescent-protein-based detection technique used to quantify protein movement rates within the cell. This method exposes a small portion of the cell to an intense laser beam. The laser beam causes permanent photobleaching of the fluorophore-tagged proteins in the exposed region. As the bleached...